High heels without heels: architectural fashion 2018

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"Brassiere" redirects here. For the type of restaurant, see.

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A bra (), short for brassiere (, UK or ), is a designed to support or cover the wearer's.,, and may have built-in breast support.

Bras are complex garments made of many parts. Most come in 36 ; standards and methods of measurement vary widely. Up to 85 per cent of women may be wearing the wrong size.



Bodice (: brassière) from 1900

The term brassiere was used by the Evening Herald in Syracuse, New York, in 1893. It gained wider acceptance in 1904 when the DeBevoise Company used it in their advertising copy—although the word is actually Norman French for a child's undershirt. In French, it is called a soutien-gorge (literally, "throat-supporter"). It and other early versions resembled a stiffened with boning.

magazine first used the term brassiere in 1907, and by 1911 the word had made its way into the. On 3 November 1914, the newly formed US patent category for "brassieres" was inaugurated with the first patent issued to. In the 1930s brassiere was gradually shortened to bra.


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Wearing a garment to support the breasts may date back to. Women wore an apodesmos, later stēthodesmē,mastodesmos and mastodeton, all meaning "breast-band", a band of wool or linen that was wrapped across the breasts and tied or pinned at the back. Roman women wore breast-bands during sport, such as those shown on the mosaic (also known as the "Bikini mosaic").

Roman women wearing breast-bands during sport,, Sicily, 4th century AD

Fragments of linen textiles found in in Austria dated to between 1440 and 1485 are believed to have been bras. Two of them had cups made from two pieces of linen sewn with fabric that extended to the bottom of the torso with a row of six eyelets for fastening with a lace or string. One had two shoulder straps and was decorated with lace in the cleavage.

From the 16th century, the undergarments of wealthier women in the Western world were dominated by the, which pushed the breasts upwards. In the later 19th century, clothing designers began experimenting with alternatives, splitting the corset into multiple parts: a -like restraining device for the lower torso, and devices that suspended the breasts from the shoulder to the upper torso.

Women have played a large part in the design and manufacture of the bra, accounting for half the patents filed. The -based German, Christine Hardt, patented the first modern brassiere in 1899. Sigmund Lindauer from Stuttgart-Bad Cannstatt, Germany, developed a brassiere for mass production in 1912 and patented it in 1913. It was mass-produced by Mechanische Trikotweberei Ludwig Maier und Cie. in Böblingen, Germany.[] In the United States, received a patent in 1914 for the first brassiere design that is recognized as the basis for modern bras. Mass production in the early 20th century made the garment widely available to women in the United States, England, Western Europe, and other countries influenced by western fashion. Metal shortages in World War I encouraged the end of the corset.

Brassieres were initially manufactured by small production companies and supplied to retailers. The term "cup" was not used until 1916, and manufacturers relied on stretchable cups to accommodate different sized breasts. Women with larger or pendulous breasts had the choice of long-line bras, built-up backs, wedge-shaped inserts between the cups, wider straps, power Lastex, firm bands under the cup, and light boning.[]

In October 1932, the S.H. Camp and Company correlated the size and pendulousness of breasts to letters A through D. Camp's advertising featured letter-labeled profiles of breasts in the February 1933 issue of Corset and Underwear Review. In 1937, Warner began to feature cup sizing in its products. Adjustable bands were introduced using multiple hook and eye closures in the 1930s. By the time World War II ended, most fashion-conscious women in Europe and North America were wearing brassieres, and women in Asia, Africa, and Latin America began to adopt it.

An that the brassiere was invented by a man named ("tit sling") who lost a lawsuit with Phillip de Brassiere ("fill up the brassiere") originated with the 1971 book Bust-Up: The Uplifting Tale of Otto Titzling and the Development of the Bra and was propagated in a comedic song from the movie.


In employers and companies are permitted to require their female employees to wear a brassiere as part of the dress code, and may sack female employees who do not wear them.



A seamstress sews a bra in Puerto Rico

Mass-produced bras are manufactured to fit a prototypical woman standing with both arms at her sides. The design assumes that both breasts are equally sized and symmetrical.

A bra is one of the most complicated garments to make. A typical design has between 20 and 48 parts, including the band, hooks, cups, lining, and straps. Bras are built on a square frame model. Lingerie designer Chantal Thomass said,

It's a highly technical garment, made of lots of tiny pieces of fabric, with so many sizes to consider for the different cups, etc. It's a garment you wash every day, so the seams and structure need to be extremely robust. It's very different from a piece of clothing; it's in direct contact with the skin, it needs to be super solid.

The bra's main components are a chest band that wraps around the torso, two cups, and. The chest band is usually closed in the back by a hook and eye, but may be fastened at the front. Sleep bras or do not have fasteners and are pulled on over the head and breasts. The section between the cups is called a gore. The section under the armpit where the band joins the cups is called the "back wing".

Bra components, including the cup top and bottom (if seamed), the central, side and back panels, and straps, are cut to manufacturer's specifications. Many layers of fabric may be cut at the same time using computer-controlled lasers or bandsaw shearing devices. The pieces are assembled by piece workers using industrial sewing machines or automated machines. Coated metal hooks and eyes are sewn in by machine and heat processed or ironed into the back ends of the band and a tag or label is attached or printed onto the bra itself. The completed bras are folded (mechanically or manually), and packaged for shipment.

The chest band and cups, not the shoulder straps, are designed to support the weight of women's breasts. Strapless bras rely on an and additional seaming and stiffening panels to support them. The shoulder straps of some sports bras cross over at the back to take the pressure off the shoulders when arms are raised. Manufacturers continually experiment with proprietary frame designs. For example, the Playtex "18-Hour Bra" model utilizes an M-Frame design.


Selection of bras in, Egypt, 2013

Bras were originally made of linen, cotton broadcloth, and twill weaves and sewn using flat-felled or bias-tape seams. They are now made of a variety of materials, including,, Spanette,,,,, foam, mesh, and, which are blended to achieve specific purposes. Spandex, a synthetic fiber with built-in "stretch memory", can be blended with cotton, polyester, or nylon. Mesh is a high-tech synthetic composed of ultra-fine filaments that are tightly knit for smoothness.

Sixty to seventy per cent of bras sold in the UK and US have cups. The underwire is made of metal, plastic, or resin. Underwire is built around the perimeter of the cup where it attaches to the band, increasing its rigidity to improve support, lift, and separation.

Wirefree or softcup bras have additional seaming and internal reinforcement. T-shirt bras utilize molded cups that eliminate seams and hide nipples. Others use padding or shaping materials to enhance bust size or cleavage.


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In most countries, bras come in a band and cup size, such as 34C; 34 is the band width, which is the measurement directly underneath the breasts, and C is the cup size, which refers to the volume of the breasts. Most bras are offered in 36 sizes; the Triumph "Doreen" comes in 67 sizes, up to 46J.Bra cup size is relative to the band size, as the volume of a woman's breast changes with the dimension of her chest. A B cup on a 34 band is not the same size as a B cup on a 36 band. In countries that have adopted the European dress-size standard, the measurement is rounded to the nearest multiple of 5 centimetres (2.0 in).

Measuring cup and band size

A poorly fitted bra can cause back and neck pain. Women with larger breasts tend to buy bras that are too small, while smaller-breasted women do the opposite. Because manufacturing standards vary widely, finding a correctly fitting bra is difficult. Women tend to find a bra that appears to fit and stay with that size, even though they may lose and gain weight. In a survey in the United Kingdom, 60 per cent of over 2,000 women between the ages of 16 to 75 said they had had a bra fitting, and 99 per cent said that fit was the least important factor when selecting a bra. Increased publicity about the issue of poorly fitted bras has increased the number of women seeking a fitting. The UK retailer stated that about 8,000 women are fitted for bras in their stores weekly. Despite this, about 80–85 per cent of women still wear the wrong bra size.

Bra experts recommend professional bra fittings from the lingerie department of a clothing store or a specialty lingerie store, especially for cup sizes D or larger, and particularly if there has been significant weight gain or loss, or if the wearer is continually adjusting her bra. Women in the UK change their bra size on average six times over their lifetimes.

Bra extension for the band

Signs of a loose bra band include the band riding up the back. If the band causes flesh to spill over the edges, it is too small. A woman can test whether a bra band is too tight or loose by reversing the bra on her torso so that the cups are in the back and then check for fit and comfort. Experts suggest that women choose a band size that fits using the outermost set of hooks. This allows the wearer to use the tighter hooks as the bra stretches during its lifetime.


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Bras may be designed to enhance a woman's breast size, or to create, or for other aesthetic, fashion or more practical considerations. are designed to aid. Compression bras, such as, push against and minimize breast movement, whereas encapsulation bras have cups for support. Breast support may be built into some swimsuits, camisoles and dresses.

Bras come in a variety of styles, including backless, balconette, convertible, shelf, full cup, demi-cup, minimizing, padded, plunge, posture, push-up, racerback, sheer, strapless, T-shirt, underwire, unlined, and soft cup.



While there are medical and surgical needs for brassieres, most are worn for fashion or cultural reasons. Women's choices about what bra to wear are consciously and unconsciously affected by social perceptions of the ideal, which changes over time. As lingerie, bras are also about expressing female sex appeal and expressions of sexual fantasy. Bras are also used to make a statement as evidenced by Jean Paul Gautier's designs and Madonna's Blond Ambition Tour.

In the 1920s in the United States, the fashion was to flatten the breasts as typified in the era. During the 1940s and 1950s, the became fashionable, supported by a (known also as a torpedo or cone bra) as worn by and. In the early 1960s, smaller breasts gained popularity, and in the late 1990s larger breasts became more fashionable. described preferences in the United States in 1990: "round, sitting high on the chest, large but not bulbous, with the look of firmness." This is regarded as contradictory in several ways.

As outerwear, bras in the form of bikini tops in the 1950s became the acceptable public display in modern times. During the 1960s, designers and manufacturers introduced padded and underwire bras. After the in September 1968, manufacturers were concerned that women would stop wearing bras. In response, many altered their marketing and claimed that wearing their bra was like "not wearing a bra". In the 1970s women sought more comfortable and natural-looking bras.

commissions a fantasy bra every fall. In 2003 it hired the jeweller to design one containing more than 2500 carats of diamonds and sapphires; valued at US million, it was the world's most valuable bra at the time.

Undergarment as outerwear[]

See also:

It became fashionable from the early 1990s to wear clothing that showed bra straps., in particular, are often worn as outerwear.'s fall 2013 couture collection featured fashions that were open in the front, revealing underwire bras.

was one of the first to start showing her bra straps, in the late 1980s. A corset she wore as outerwear during her 1990 sold for US,000 in 2012 at the Christie's Pop Culture auction in London.

Wearing clothes that reveal the bra or straps became so common that Cosmopolitan created guidelines in 2012 on how to expose them. Advice included avoiding plain, flesh-toned, smooth-cup bras, so that the exposure does not appear accidental; making sure the bra is in good condition; and wearing a style that either matches the colour of the outerwear or is dramatically different.


Bras are not worn around the world; in some third-world countries bras may cost up to 10–30 hours of a woman's wages, making them unaffordable to most of the population. As of 2011, women in needed to pay up to a week's wages for a new bra. Bras are highly prized at second-hand markets in. The Uplift Project provides recycled bras to women in developing countries. Since 2005 they have shipped 330,000, including to Fiji, Vanuatu, Tonga, and Cambodia.

In 2009 Somalia's hard-line Islamic group forced women to shake their breasts at gunpoint to see if they were wearing bras, which they called "un-Islamic". A resident of whose daughters were whipped said, "The Islamists say a woman's chest should be firm naturally, or flat." In 2009, Elena Bodnar invented the Emergency Bra, which doubles as a gas mask; she came up with the idea when as a young doctor she witnessed the Chernobyl nuclear disaster. She received the Public Health Prize for her design.

Surveys have reported that 5–25 per cent of Western women do not wear a bra. A commissioned by asked more than 1,000 women what they like in a bra. Among the respondents, 67 per cent said they prefer wearing a bra to going braless, while 85 per cent wanted to wear a "shape-enhancing bra that feels like nothing at all." They were split as regards underwire bras: 49 per cent said they prefer underwire bras, the same percentage as those who said they prefer wireless bras.

According to underwire manufacturer S & S Industries of New York, who supply bras to,,,,, and other labels, about 70 per cent of bra-wearing women wear underwire bras.

In an online survey for magazine in 2013, 25 per cent of women reported that they do not wear a bra every day. A "National No-Bra Day" was first observed in the United States on 9 July in 2011. Women posted on Twitter about the relief they feel when taking off their bra. More than 250,000 people expressed an interest in "attending" the day on a Facebook page.

Wearing a bra does not prevent breasts from sagging. Many women, in the mistaken belief that breasts cannot anatomically support themselves, think that wearing a will prevent their breasts from sagging later in life. Researchers, bra manufacturers, and health professionals cannot find any evidence to support the idea that wearing a bra for any amount of time slows breast ptosis.Bra manufacturers are careful to claim that bras only affect the shape of breasts while they are being worn.

Economic impact[]

Consumers spend around  billion a year worldwide on bras. In the US during 2012, women owned an average of nine bras and wore six on a regular basis. That increased from 2006, when the average American woman owned six, one of which was strapless, and one in a colour other than white. British women in a 2009 survey reported that they owned an average of 16 bras.

The average bra size among North American women has changed from 34B in 1983 to a 34DD in 2012–2013, and from 36C last year[] to 36DD in the UK during 2014–2015. The change in bra size has been linked to growing obesity rates, breast implants, increased birth control usage, estrogen mimicking pollutants, the availability of a larger selection of bras, and women wearing better fitting bras.

Bra shirt with built-in support, 2015

Bras are made in Asian countries, including Sri Lanka, India, and China. While there has been some social pressure from the and on manufacturers to reduce use of labour, most major apparel manufacturers rely on them directly and indirectly. Prior to 2005, a trade agreement limited textile imports to the European Union and the US. China was exporting US.9 billion in textiles and clothing each year to the EU and the US. When those quotas expired on 1 January 2005, the so-called Bra Wars began. Within six months, China shipped 30 million more bras to the two markets: 33 per cent more to the US and 63 per cent more to the EU. As of 2014, an average bra cost £29.80. As of 2012, Africa imported US7 million worth of bras, with South Africa accounting for 40 per cent. Morocco was second and Nigeria third, while Mauritius topped purchasing on a basis.

In countries where labour costs are low, bras that cost US–7 to manufacture sell for US or more in American retail stores. As of 2006, female garment workers in Sri Lanka earned about US.20 per day. Similarly, Honduran garment factory workers in 2003 were paid US

We review the normal anatomy of the white matter (WM) tracts as they appear on directional diffusion tensor imaging (DTI) color maps, which will almost certainly be available to the general radiologist as part of a commercial DTI software package in the near future. Anatomic drawings and gross dissection photographs are correlated with the directional DTI color maps to review the anatomy of those tracts readily seen in most cases. We also include several correlative examples of so-called tractograms in which specific tracts are traced and displayed by using computer-graphical techniques (). Since several excellent reviews focusing on tractography and other sophisticated DTI postprocessing techniques are already published (–), we focus on the directional eigenvector color maps. A brief review of the basic principles underlying DTI is also included; several more comprehensive reviews are available for the reader who wishes to delve deeper into the technical aspects of DTI (, ). Finally, we briefly review the DTI patterns that result when a cerebral neoplasm involves WM tracts; knowledge of these patterns becomes critically important when neurosurgeons use DTI in planning tumor resections, as they frequently do at our institution (, ).

The Physics of DTI

By applying the appropriate magnetic field gradients, MR imaging may be sensitized to the random, thermally driven motion (diffusion) of water molecules in the direction of the field gradient. Diffusion is anisotropic (directionally dependent) in WM fiber tracts, as axonal membranes and myelin sheaths present barriers to the motion of water molecules in directions not parallel to their own orientation. The direction of maximum diffusivity has been shown to coincide with the WM fiber tract orientation (). This information is contained in the diffusion tensor, a mathematic model of diffusion in three-dimensional space. In general, a tensor is a rather abstract mathematic entity having specific properties that enable complex physical phenomena to be quantified. In the present context, the tensor is simply a matrix of numbers derived from diffusion measurements in several different directions, from which one can estimate the diffusivity in any arbitrary direction or determine the direction of maximum diffusivity.

The tensor matrix may be easily visualized as an ellipsoid whose diameter in any direction estimates the diffusivity in that direction and whose major principle axis is oriented in the direction of maximum diffusivity () (). With use of DTI, both the degree of anisotropy and the local fiber direction can be mapped voxel by voxel, providing a new and unique opportunity for studying WM architecture in vivo.

Fig 1. Fig 1.

Top left, Fiber tracts have an arbitrary orientation with respect to scanner geometry (x, y, z axes) and impose directional dependence (anisotropy) on diffusion measurements.

Top right, The three-dimensional diffusivity is modeled as an ellipsoid whose orientation is characterized by three eigenvectors (ϵ1, ϵ2, ϵ3) and whose shape is characterized three eigenvalues (λ1, λ2, λ3). The eigenvectors represent the major, medium, and minor priniciple axes of the ellipsoid, and the eigenvalues represent the diffusivities in these three directions, respectively.

Bottom, This ellipsoid model is fitted to a set of at least six noncollinear diffusion measurements by solving a set of matrix equations involving the diffusivities (ADC’s) and requiring a procedure known as matrix diagonalization. The major eigenvector (that eigenvector associated with the largest of the three eigenvalues) reflects the direction of maximum diffusivity, which, in turn, reflects the orientation of fiber tracts. Superscript T indicates the matrix transpose.

The tensor model of diffusion consists of a 3 × 3 matrix derived from diffusivity measurements in at least six noncollinear directions. The tensor matrix is diagonally symmetric (Dij = Dji) with six degrees of freedom (ie, only six of the tensor matrix’s nine entries are independent and so the matrix is fully determined by these six parameters), such that a minimum of six diffusion-encoded measurements are required to accurately describe the tensor. Using more than six encoding directions will improve the accuracy of the tensor measurement for any arbitrary orientation (–).

The tensor matrix is subjected to a linear algebraic procedure known as diagonalization, the result of which is a set of three eigenvectors representing the major, medium, and minor principle axes of the ellipsoid fitted to the data and the corresponding three eigenvalues (λ1, λ2, λ3), which represent the apparent diffusivities along these axes. (The word eigen is Germanic in origin, meaning “peculiar” or “special.” The term eigenvalue was used by British algebraists in the late 19th century to refer to a “characteristic value” of a matrix; specifically, a number k is called an eigenvalue of the matrix A if there exists a nonzero vector v such that Av = kv. In this case, the vector v is called an eigenvector of A corresponding to k [].) This procedure may be thought of as a rotation of the x, y, and z coordinate system in which the data were acquired (dictated by scanner geometry) to a new coordinate system whose axes are dictated by the directional diffusivity information ().

Diffusion anisotropy is easily understood as the extent to which the shape of the tensor ellipsoid deviates from that of a sphere; mathematically, this translates to the degree to which the three tensor eigenvalues differ from one another. Any of several anisotropy metrics may be used, one of the most common being fractional anisotropy (FA) (), which derives from the standard deviation of the three eigenvalues and ranges from 0 (isotropy) to 1 (maximum anisotropy): Math1 where λ̄ denotes the mean of the three eigenvalues, which is equal to the directionally averaged diffusivity. The direction of maximum diffusivity may be mapped by using red, green, and blue (RGB) color channels with color brightness modulated by FA, resulting in a convenient summary map from which the degree of anisotropy and the local fiber direction can be determined () ().

Fig 2. Fig 2.

A, FA map without directional information.

B, Combined FA and directional map. Color hue indicates direction as follows: red, left-right; green, anteroposterior; blue, superior-inferior. This convention applies to all the directional maps in this review. Brightness is proportional to FA.


DTI MR Acquisition and Directional Mapping

DTI MR images for this review were obtained with a 1.5-T system (GE Medical Systems, Milwaukee, WI) by using a quadrature birdcage head coil, single-shot echo planar imaging sequence (4500/71.8/4 [TR/TE/excitations], 240-mm field of view, 3-mm sections, 2 slabs, 20 sections per slab), matrix 128 × 128 zero-filled to 256 × 256, voxel size 1.87 × 1.87 × 3.0 mm interpolated to 0.94 mm isotropic, diffusion encoding in 23 directions (minimum energy optimization []) with b = 0, 1000 s/mm2, postprocessing with Automated Image Registration (), a 3 × 3 in-plane spatial median filter, tensor decoding and diagonalization (, ). The choice of 23 directions represented a somewhat arbitrary balance between accuracy in fitting the tensor model (increasing the number of encoding directions decreases the variance in the tensor model parameters) and the number of sections that could be acquired (our imaging system limits the number of images per series to 512). The eigenvalues and eigenvectors of the diffusion tensor were used to calculate maps of the diffusion tensor trace, FA, and vector orientation maps, which were generated by mapping the major eigenvector directional components in x, y, and z into RGB color channels and weighting the color brightness by FA. The convention we used for directional RGB color mapping is red for left-right, green for anteroposterior, and blue for superior-inferior.

DTI Tractograms

The WM tracts were estimated with tractography by using the previously described tensor deflection (TEND) algorithm (). Tracking was initiated from a start location (or seed point) in both forward and backward directions defined by the major eigenvector at the seed point. The propagation was terminated when the tract trajectory reached a voxel with FA less than 0.2 (the estimated major eigenvector direction becomes less accurate as FA decreases and becomes very sensitive to image noise for FA less than 0.2) or when the angle between two consecutive steps was greater than 45°.

A complete set of fiber trajectories was obtained by placing seeds in all the voxels with FA greater than 0.4 (the estimation of major eigenvector direction for voxels with FA greater than 0.4 is expected to be sufficiently accurate to yield a good estimate of local fiber direction). Estimates of white matter pathways were generated from the center of each seed voxel. A specific tract or fasciculus was separated from the complete set of trajectories by retaining those fibers that intersected predefined regions of interest (ROIs). The ROIs were chosen to enclose tract cross sections that were visible in any of the axial, sagittal, or coronal directional color maps (, ). Corpus callosum was selected by using the apparent tract cross section in the midsagittal plane. The anterior commissure was also selected by using an ROI placed in sagittal cross section; subsequently, only the branches that reached the temporal lobes were retained. The corticospinal tract was obtained by selecting the fibers emerging from the motor cortex and reaching the basis pedunculi. The tracts of the internal capsule were selected in an axial plane situated about halfway through the midbrain. The association fiber tracts were selected by using procedures similar to those described by Lazar et al ().

Fiber trajectories are displayed with colors overlaid onto gray-scale anatomic images in various three-dimensional projections. Note that, unlike the directional color maps in which directional information is color-coded, individual tractograms are displayed by using fixed colors chosen arbitrarily.

Gross Dissections

Brain specimens were removed fresh at autopsy (before fixation) and were stored in a 10% formalin bath until final preparation for dissection. Brains that were not damaged in the area of the planned dissection were rinsed for 1 hour in room- temperature tap water and then were frozen in water in a −20°C freezer for 1 week. At the end of the week, the frozen brain was rinsed with lukewarm tap water until completely thawed (about 1 hour) and then refrozen in water for another week. This process was repeated such that the brain was rinsed and thawed 3 times in total. The entire preparatory process took 3 weeks before dissection could be performed. As many dissections could not be completed in a single sitting, the unfinished specimens were placed in 5% formalin until completed, and then stored in a 10% formalin solution when done.


Correlative line drawings of major tracts have been reproduced from A Functional Approach to Neuroanatomy () with permission from the publisher.

WM Fiber Classification

WM fiber tracts traditionally have been classified as follows: Association fibers interconnect cortical areas in each hemisphere. Fibers of this type typically identified on DTI color maps include cingulum, superior and inferior occipitofrontal fasciculi, uncinate fasciculus, superior longitudinal (arcuate) fasciculus, and inferior longitudinal (occipitotemporal) fasciculus. Projection fibers interconnect cortical areas with deep nuclei, brain stem, cerebellum, and spinal cord. There are both efferent (corticofugal) and afferent (corticopetal) projection fibers. Fibers of this type typically identified on DTI color maps include the corticospinal, corticobulbar, and corticopontine tracts, as well as the geniculocalcarine tracts (optic radiations). Commissural fibers interconnect similar cortical areas between opposite hemispheres. Fibers of this type typically identified on DTI color maps include corpus callosum and anterior commissure.

Other tracts that are occasionally, but not consistently, identified on directional DTI color maps include optic tract, fornix, tapetum, and many fibers of the brain stem and cerebellum. Space limitations preclude a comprehensive review of all tracts potentially visualized with DTI. Rather, we focus on the major tracts that are consistently identified in our practice.

Association Fibers

Cingulum (, , and ).—

Fig 3. Fig 3.

A, Illustration shows the anatomic relationships of several WM fiber tracts in the coronal plane. Circled tracts are those further illustrated in this review. The corpus callosum is “sandwiched” between the cingulum superomedially and the superior occipitofrontal fasciculus inferolaterally. The superior longitudinal fasciculus sweeps along the superior margin of the claustrum in a great arc. The inferior occipitofrontal fasciculus lies along the inferolateral edge of the claustrum. (Reproduced with permission from reference 20.)

B, Directional map corresponding to A. The paired cingula are easily identified in green (yellow arrows) just cephalad to the red corpus callosum (thick white arrow). White arrowheads indicate superior occipitofrontal fasciculus; thin white arrows, inferior occipitofrontal fasciculus; yellow arrowheads, superior longitudinal fasciculus. Like the corpus callosum, the commissural fibers of the anterior commissure are left-right oriented toward the midline, resulting in the characteristic red (open arrows) on this DTI map. Further lateral, the fibers diverge and mingle with other tracts; they are no longer identifiable with DTI, but can be traced with tractography.

Fig 4. Fig 4.

Cingulum, sagittal view.

A, Illustration shows the cingulum arching over the corpus callosum.

B, Gross dissection, median view.

C, Directional map. Because DTI reflects tract orientation voxel by voxel, the color changes from green to blue as the cingulum (arrows) arches around the genu and splenium (arrowheads). Green indicates anteroposterior; red, left-right; blue, superior-inferior.

D, Tractogram. (See also , axial directional map.)

Fig 5. Fig 5.

A, Cingulum, axial directional map. The paired cingula (arrowheads) are easily identified in green on this section obtained just cephalad to the corpus callosum.

B, Inferior occipitofrontal fasciculus (white arrows) and inferior longitudinal fasciculus (yellow arrow), axial directional map. The inferior occipitofrontal fasciculus lies in a roughly axial plane and is easily identified in green; it connects frontal and occipital lobes at the level of the midbrain. Posteriorly, the inferior occipitofrontal fasciculus mingles with the inferior longitudinal fasciculus, optic radiations, superior longitudinal fasciculus, and other fibers to form the sagittal stratum—a vast and complex bundle that connects the occipital lobe to the rest of the brain.

The cingulum begins in the parolfactory area of the cortex below the rostrum of the corpus callosum, then courses within the cingulate gyrus, and, arching around the entire corpus callosum, extends forward into the parahippocampal gyrus and uncus. It interconnects portions of the frontal, parietal, and temporal lobes. Its arching course over the corpus callosum resembles the palm of an open hand with fingertips wrapping beneath the rostrum of the corpus callosum.

Superior Occipitofrontal Fasciculus (, ).—

Fig 6. Fig 6.

Superior and inferior occipitofrontal fasciculi and uncinate fasciculus, sagittal view.

A, Illustration shows the superior occipitofrontal fasciculus arching over the caudate nucleus to connect frontal and occipital lobes, and the uncinate fasciculus hooking around the lateral sulcus to connect inferior frontal and anterior temporal lobes (see also uncinate fasciculus in and ).

B, Gross dissection, lateral view. Like the superior occipitofrontal fasciculus, the inferior occipitofrontal fasciculus connects the frontal and occipital lobes, but it lies more caudad, running inferolateral to the claustrum (see also for axial view). The middle portion of the inferior occipitofrontal fasciculus is bundled together with the middle portion of the uncinate fasciculus.

C and D, Tractograms of the superior (C) and inferior (D) occipitofrontal fasciculi.

Whereas the cingulum wraps around the superior aspect of the corpus callosum, the superior occipitofrontal fasciculus lies beneath it. It connects occipital and frontal lobes, extending posteriorly along the dorsal border of the caudate nucleus. Portions of the superior occipitofrontal fasciculus parallel the superior longitudinal fasciculus (see below), but they are separated from the superior longitudinal fasciculus by the corona radiata and internal capsule.

Inferior Occipitofrontal Fasciculus (, , ).—

The inferior occipitofrontal fasciculus also connects the occipital and frontal lobes but is far inferior compared with the superior occipitofrontal fasciculus. It extends along the inferolateral edge of the claustrum, below the insula. Posteriorly, the inferior occipitofrontal fasciculus joins the inferior longitudinal fasciculus, the descending portion of the superior longitudinal fasciculus, and portions of the geniculocalcarine tract to form most of the sagittal stratum, a large and complex bundle that connects the occipital lobe to the rest of the brain. The middle portion of the inferior occipitofrontal fasciculus is bundled together with the middle portion of the uncinate fasciculus (see below).

Uncinate Fasciculus (, , , ).—

Fig 7. Fig 7.

Uncinate fasciculus and superior longitudinal fasciculus, sagittal view.

A, Illustration shows the uncinate fasciculus hooks around the lateral sulcus to connect inferior frontal and anterior temporal lobes.

B, Tractogram. (See also for gross dissection.)

Fig 8. Fig 8.

Superior longitudinal fasciculus, sagittal view. This massive fiber bundle sweeps along the superior margin of the claustrum in a great arc. The term arcuate fasciculus is often used in reference to the superior longitudinal fasciculus or, specifically, its more arcuate portion.

A, Gross dissection, lateral view.

B, Directional map, parasagittal section. Note the color change from green to blue as the superior longitudinal fasciculus fibers turn from an anteroposterior orientation (white arrows) to a more superior-inferior orientation (arrowhead). The same phenomenon can also be seen in the uncinate fasciculus (yellow arrow).

C, Tractogram. (See also .)

Uncinate is from the Latin uncus meaning “hook.” The uncinate fasciculus hooks around the lateral fissure to connect the orbital and inferior frontal gyri of the frontal lobe to the anterior temporal lobe. The anterior aspect of this relatively short tract parallels, and lies just inferomedial to, the inferior occipitofrontal fasciculus. Its midportion actuallyadjoins the middle part of the inferior occipitofrontal fasciculus before heading inferolaterally into the anterior temporal lobe.

Superior Longitudinal (arcuate) Fasciculus (, , ).—

The superior longitudinal fasciculus is a massive bundle of association fibers that sweeps along the superior margin of the insula in a great arc, gathering and shedding fibers along the way to connect frontal lobe cortex to parietal, temporal, and occipital lobe cortices. The superior longitudinal fasciculus is the largest association bundle.

Inferior Longitudinal (occipitotemporal) Fasciculus ( and ).—

Fig 9. Fig 9.

Inferior longitudinal (occipitotemporal) fasciculus.

A, Directional map, parasagittal section, shows the inferior longitudinal fasciculus (arrow).

B, Tractogram. (See also for gross dissection and for axial directional map.)

The inferior longitudinal fasciculus connects temporal and occipital lobe cortices. This tract traverses the length of the temporal lobe and joins with the inferior occipitofrontal fasciculus, the inferior aspect of the superior longitudinal fasciculus, and the optic radiations to form much of the sagittal stratum traversing the occipital lobe.

Projection Fibers

Corticospinal, Corticopontine, and Corticobulbar Tracts ().—

Fig 10. Fig 10.

Corticospinal tract.

A, Illustration. (Twisting of the tract superior to the internal capsule not shown.) Corticospinal fibers originating along the motor cortex converge through the corona radiata and posterior limb of the internal capsule on their way to the lateral funiculus of the spinal cord.

B, Coronal directional map. Corticospinal fibers (arrows) are easily identified in blue on this DTI map owing to their predominantly superior-inferior orientation. The fibers take on a more violet hue as they turn medially to enter the cerebral peduncles, then become blue again as they descend through the brain stem. Corticospinal fibers run with corticobulbar and corticopontine fibers; these cannot be distinguished on directional maps but can be parsed by using tractographic techniques.

C, Tractogram.

The corticospinal and corticobulbar tracts are major efferent projection fibers that connect motor cortex to the brain stem and spinal cord. Corticospinal fibers converge into the corona radiata and continue through the posterior limb of the internal capsule to the cerebral peduncle on their way to the lateral funiculus. Corticobulbar fibers converge into the corona radiata and continue through the genu of the internal capsule to the cerebral peduncle where they lie medial and dorsal to the corticospinal fibers. Corticobulbar fibers predominantly terminate at the cranial motor nuclei. These bundles run together and are not discriminated on directional DTI color maps, but can be parsed by using sophisticated tractographic algorithms ().

Corona Radiata ().—

Fig 11. Fig 11.

A and B, Illustration (A) and gross dissection, medial view (B) of the corona radiata.

C, Directional map, three adjacent parasagittal sections, with corona radiata identifiable in blue (arrows). Corona radiata fibers interdigitate with laterally directed callosal fibers, resulting in assorted colors in the vicinity of their crossing.

D, Tractogram in which different portions of the corona radiata have been parsed by initiating the tractographic algorithm from different starting locations.

Though not a specific tract per se, the corona radiata is one of the most easily identified structures on directional DTI color maps. Its coronally oriented fibers tend to give it a color quite distinct from that of surrounding tracts, which are oriented primarily light-right (corpus callosum) or anteroposteriorly (superior longitudinal fasciculus). Fibers to and from virtually all cortical areas fan out superolaterally from the internal capsule to form the corona radiata.

Internal Capsule ().—

Fig 12. Fig 12.

Internal capsule, axial view.

A and B, Illustration (A) and directional map (B). Because the anterior limb (small arrow) primarily consists of anteroposteriorly directed frontopontine and thalamocortical projections, it appears green on this DTI map. The posterior limb (large solid arrow), which contains the superior-inferiorly directed tracts of the corticospinal, corticobulbar, and corticopontine tracts, is blue. Note also the blue fibers of the external capsule (arrowhead) and the green fibers of the optic radiations (open arrow) in the retrolenticular portion of the internal capsule.

The internal capsule is a large and compact fiber bundle that serves as a major conduit of fibers to and from the cerebral cortex and is readily identified on directional DTI color maps. The anterior limb lies between the head of the caudate and the rostral aspect of the lentiform nucleus, while the posterior limb lies between the thalamus and the posterior aspect of the lentiform nucleus. The anterior limb passes projection fibers to and from the thalamus (thalamocortical projections) as well as frontopontine tracts, all of which are primarily anteroposteriorly oriented in contradistinction to the posterior limb, which passes the superior-inferiorly oriented fibers of the corticospinal, corticobulbar, and corticopontine tracts. This gives the anterior and posterior limbs distinctly different colors on directional DTI maps.

Geniculocalcarine Tract (optic radiation) ().—

Fig 13. Fig 13.

Geniculocalcarine tract (optic radiation), axial view.

A–D, Illustration (A), gross dissection (B), directional map (C), and tractogram (D). As this tract connects the lateral geniculate nucleus to occipital (primary visual) cortex, the fibers sweep around the posterior horn of the lateral ventricle and terminate in the calcarine cortex (more cephalad fibers of the optic radiation take a more direct path to the visual cortex). The optic radiation (arrows) mingles with the inferior occipitofrontal fasciculus, inferior longitudinal fasciculus, and the inferior aspect of superior longitudinal fasciculus to form much of the sagittal stratum in the occipital lobe.

The optic radiation connects the lateral geniculate nucleus to occipital (primary visual) cortex. The more inferior fibers of the optic radiation sweep around the posterior horns of the lateral ventricles and terminate in the calcarine cortex; the more superior fibers take a straighter, more direct path. The optic radiation mingles with the inferior occipitofrontal fasciculus, inferior longitudinal fasciculus, and inferior aspect of the superior longitudinal fasciculus to form much of the sagittal stratum in the occipital lobe.

Commissural Fibers

Corpus Callosum ( and ).—

Fig 14. Fig 14.

Corpus callosum, axial view.

A–D, Illustration (A), gross dissection (B), directional map (C), and tractogram (D). The largest WM fiber bundle, the corpus callosum connects corresponding areas of cortex between the hemispheres. Close to the midline, its fibers are primarily left-right oriented, resulting in its red appearance on this DTI map. However, callosal fibers fan out more laterally and intermingle with projection and association tracts, resulting in more complex color patterns.

Fig 15. Fig 15.

A and B, Sagittal directional map of the corpus callosum (arrowheads) (A) and tractogram (B). (See also .)

By far the largest WM fiber bundle, the corpus callosum is a massive accumulation of fibers connecting corresponding areas of cortex between the hemispheres. Fibers traversing the callosal body are transversely oriented, whereas those traversing the genu and splenium arch anteriorly and posteriorly to reach the anterior and posterior poles of the hemispheres. Near the midsagittal plane, all of the corpus callosum fibers are left-right oriented and easily identified on directional DTI color maps. However, as they radiate toward the cortex, callosal fibers interdigitate with association and projection fibers; resolving these fiber crossings with DTI is a difficult problem and the subject of intensive research ().

Anterior Commissure ().—

The anterior commissure crosses through the lamina terminalis. Its anterior fibers connect the olfactory bulbs and nuclei; its posterior fibers connect middle and inferior temporal gyri.

Brain Stem

The complex anatomy of the brain stem includes a large number of tracts and nuclei, as well as multiple commissures and decussations, many of which can be resolved on directional DTI color maps. Space prohibits a comprehensive review, but several commonly seen brain stem structures are illustrated in Figs 16 and .

Fig 16. Fig 16.

A and B, Axial illustration (A) and directional map (B) of the rostral midbrain.

Fig 17. Fig 17.

A and B, Axial illustration (A) and directional map (B) of the midpons.

DTI Patterns in WM Tracts Altered by Tumor

The goal of surgical treatment for cerebral neoplasms is to maximize the extent of tumor resection while minimizing postoperative neurologic deficits resulting from damage to intact, functioning brain. This requires preoperative or intraoperative mapping of the tumor and its relationship to functional structures, including cerebral cortex and WM tracts. Cortical mapping can be accomplished with either functional MR imaging or intraoperative electrocortical stimulation. These methods are inadequate, however, for depicting the relationship of tumor to WM tracts. DTI is uniquely suited for this role.

The altered states of WM resulting from cerebral neoplasm () might be expected to influence the measurement of diffusion tensor anisotropy and orientation in various ways, resulting in several possible patterns on directional DTI color maps (, ). Intact WM tracts displaced by tumor might retain their anisotropy and remain identifiable in their new location or orientation on directional DTI color maps. Edematous or tumor-infiltrated tracts might lose some anisotropy but retain enough directional organization to remain identifiable on directional DTI maps. Finally, WM tracts might be destroyed or disrupted to the point where directional organization (and, consequently, diffusion anisotropy) is lost completely.

Fig 18. Fig 18.

Potential patterns of WM fiber tract alteration by cerebral neoplasms. The extent to which these patterns can be discriminated on the basis of DTI is under investigation.

In a series of 20 brain tumors of various histologic diagnoses imaged preoperatively with DTI, we identified four major patterns in affected WM tracts, categorized on the basis of anisotropy and fiber direction or orientation ().

Pattern 1 () consists of normal or only slightly decreased FA with abnormal location and/or direction resulting from bulk mass displacement. This is the most clinically useful pattern in preoperative planning because it confirms the presence of an intact peritumoral tract that can potentially be preserved during resection ().

Fig 19. Fig 19.

DTI pattern 1: normal anisotropy, abnormal location or orientation.

A–E, T2-weighted MR image (A), contrast-enhanced T1-weighted image (B), directional maps in axial (C) and coronal (D) planes, and coronal tractogram of bilateral corticospinal tracts (E). WM tracts are deviated anteriorly, inferiorly, and posterolaterally by this ganglioglioma but retain their normal anisotropy. Therefore, they remain readily identified on DTI (C and D) and readily traced with tractography (E). The AC (red, arrowhead), IOFF (green, open arrow), and CST (blue, solid arrows) are deviated. Note the blue hue of the CST change to red as it deviates toward the axial plane by the tumor (arrow on coronal view [D]).

Pattern 2 () is substantially decreased FA with normal location and direction (ie, normal hues on directional color maps). We frequently observe this pattern in regions of vasogenic edema, although the specificity of this pattern is not yet known; further study is needed to determine the clinical utility of this observation.

Fig 20. Fig 20.

DTI pattern 2: abnormal (low) anisotropy, normal location and orientation.

A–D, T2-weighted MR image (A), contrast-enhanced T1-weighted MR image (B), FA map (C), and directional map (D). The homogeneous region of hyperintensity on the T2-weighted image represents vasogenic edema surrounding a small metastasis (on another section, not shown). Despite diminished anisotropy in this region (darker region outlined on FA map) and diminished color brightness on directional map, the involved fiber tracts retain their normal color hues on the directional map (superior longitudinal fasciculus, green, arrow; corona radiata, blue, arrowhead). This preservation of normal color hues despite a substantial decrease in anisotropy is consistent with the abnormality of vasogenic edema, which enlarges the extracellular space (allowing less restricted diffusion perpendicular to axonal fibers, thus reducing the anisotropy) without disrupting cellular membranes, leaving their directional organization intact. It is not yet known to what extent this pattern is specific for edema, however.

Pattern 3 () is substantially decreased FA with abnormal hues on directional color maps. We have identified this pattern in a small number of infiltrating gliomas in which the bulk mass effect appeared to be insufficient to account for the abnormal hues on directional maps. We speculate that infiltrating tumor disrupts the directional organization of fiber tracts to cause altered color patterns on directional maps, but this phenomenon requires further study.

Fig 21. Fig 21.

DTI pattern 3: abnormal (low) anisotropy, abnormal orientation.

A–D, T2-weighted MR image (A), contrast-enhanced T1-weighted image (B), FA map (C), and directional map (D). This infiltrating astrocytoma is characterized by both diminished anisotropy and abnormal color (arrowhead) on the directional map, suggesting disruption of WM fiber tract organization more severe and complex than that seen with pattern 2 (compare ). Note that the color change cannot easily be attributed to bulk mass effect as in purely deviated tracts.

Pattern 4 () consists of isotropic (or near-isotropic) diffusion such that the tract cannot be identified on directional color maps. This pattern is observed when some portion of a tract is completely disrupted by tumor. This pattern can be useful in preoperative planning in the sense that no special care need be taken during resection to preserve a tract that is shown by DTI to be destroyed.

Fig 22. Fig 22.

DTI pattern 4: near-zero anisotropy, tract unidentifiable.

A–D, T2-weighted MR image (A), contrast-enhanced T1-weighted image (B), FA map (C), and directional map (D). This high-grade astrocytoma has destroyed the body of the corpus callosum, rendering the diffusion essentially isotropic and precluding identification on the directional map (arrow).

It should be noted that combinations of the above patterns may occur; for example, a combination of patterns 1 and 2 may be observed in a tract that is both displaced and edematous.


The polychrome produced by mapping the direction of the diffusion tensor allows rapid and unprecedented visualization of WM tracts in vivo. There is order to the complex beauty of these maps, and their interpretation requires knowledge of fiber tract anatomy that has heretofore not been commonly applied in routine clinical imaging. As DTI rapidly makes its way into the clinical realm, we have attempted to provide a concise pictorial review of the major tract anatomy typically visualized on directional DTI color maps without the more advanced and sophisticated tractographic techniques that will take somewhat longer to reach routine clinical practice. We hope this review is useful to those radiologists who already interpret DTI maps and will inspire those who have not yet incorporated DTI into their practice to do so.


The authors gratefully acknowledge Drs. Konstantinos Arfanakis, Behnam Badie, Brian Witwer, Yijing Wu, and Sandra Zegarra for their assistance on this project.


  • Supported in part by National Institute of Mental Health grant RO1 MH62015.

    Presented in part as an education exhibit at the 88th annual meeting of the Radiological Society of North America, Chicago, IL, December 1–6, 2002.


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  • Received June 8, 2003.
  • Accepted after revision August 7, 2003.
.24 for each sweatshirt they made, less than one-half of one per cent of the retail price. In 2009, residents in the textile manufacturing city of in the province of China made more than 200 million bras. Children were employed to assemble bras and were paid 0.30 for every 100 bra straps they helped assemble. In one day they could earn 20 to 30 yuan.


Informal surveys have found that many women began wearing bras to be fashionable, to conform to social or maternal pressure, or for physical support. Women sometimes wear bras because they mistakenly believe they prevent.[] Very few cited comfort as the reason. While many Western women recognize that they have been socialized to wear bras, they may report feeling exposed or "subject to violation" without one, or that wearing one improves their appearance.

Feminist opinions[]

The feminist bra-burning (see below) finds an echo in an earlier generation of feminists who called for burning corsets as a step toward liberation. In 1873 wrote:

So burn up the corsets! ... No, nor do you save the whalebones, you will never need whalebones again. Make a bonfire of the cruel steels that have lorded it over your thorax and abdomens for so many years and heave a sigh of relief, for your emancipation I assure you, from this moment has begun.

Some feminists began arguing in the 1960s and 1970s that the bra was an example of how women's clothing shaped and even deformed women's bodies to male expectations. Professor listened to feminist talk about bras during a formal college dinner in, in 1964 (Greer had become a member of that college in 1962):

At the graduates' table, Germaine was explaining that there could be no liberation for women, no matter how highly educated, as long as we were required to cram our breasts into bras constructed like mini-Vesuviuses, two stitched white cantilevered cones which bore no resemblance to the female anatomy. The willingly suffered discomfort of the Sixties bra, she opined vigorously, was a hideous symbol of female oppression.

In 1968 at the feminist, protestors symbolically threw a number of feminine products into a "Freedom Trash Can". These included bras, which were among items the protestors called "instruments of female torture" and accoutrements of what they perceived to be enforced. A local news story in the Atlantic City Press erroneously reported that "the bras, girdles, falsies, curlers, and copies of popular women's magazines burned in the 'Freedom Trash Can'". Individuals who were present said that no one burned a bra nor did anyone take off her bra. However, a female reporter (Lindsy Van Gelder) covering the protest drew an analogy between the feminist protesters and protesters who, and the parallel between protesters burning their draft cards and women burning their bras was encouraged by some organizers including. "The media picked up on the bra part", said later. "I often say that if they had called us 'girdle burners,' every woman in America would have run to join us."

Feminism and "bra-burning" became linked in popular culture. The analogous term jockstrap-burning has since been coined as a reference to. While feminist women did not literally burn their bras, some stopped wearing them in protest. The feminist author Bonnie J. Dow has suggested that the association between feminism and bra-burning was encouraged by individuals who opposed the feminist movement. "Bra-burning" created an image that women weren't really seeking freedom from sexism, but were attempting to assert themselves as sexual beings. This might lead individuals to believe, as wrote, that the women were merely trying to be "trendy, and to attract men." Some feminist activists believe that use the bra burning myth and the subject of going braless to trivialize what the protesters were trying to accomplish at the feminist 1968 and the feminist movement in general.

's book (1970) became associated with the anti-bra movement because she pointed out how restrictive and uncomfortable a bra could be. "Bras are a ludicrous invention", she wrote, "but if you make bralessness a rule, you're just subjecting yourself to yet another repression."

in her book Femininity (1984) took the position that women without bras shock and anger men because men "implicitly think that they own breasts and that only they should remove bras."

The feminist author wrote in 2005 that the bra "serves as a barrier to touch" and that a braless woman is "", eliminating the "hard, pointy look that phallic culture posits as the norm." Without a bra, in her view, women's breasts are not consistently shaped objects but change as the woman moves, reflecting the natural body. Other feminist anti-bra arguments from Young in 2005 include that are used to indoctrinate girls into thinking about their breasts as sexual objects and to accentuate their sexuality. Young also wrote in 2007 that, in American culture, breasts are subject to "[c]apitalist, American media-dominated culture [that] objectifies breasts before such a distancing glance that freezes and masters." The academic Wendy Burns-Ardolino wrote in 2007 that women's decision to wear bras is mediated by the "".

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Further reading[]

Casselman, Anne (2005).. Discover. Vol. 26 no. 11. Chicago. pp. 18–19.  . Retrieved 27 April 2018.  Ewing, Elizabeth (1971). Fashion in Underwear. London: Batsford.  .  Freeman, Susan K. (2004). "In Style: Femininity and Fashion Since the Victorian Era". Journal of Women's History. 16 (4): 191–206. :.  . . BBC News. 10 December 2007. Retrieved 27 April 2018.  ; Lindsey, Karen (2000). Dr. Susan Love's Breast Book (3rd ed.). Cambridge, Massachusetts: Perseus Publishing.  .  Pedersen, Stephanie (2004). Bra: A Thousand Years of Style, Support and Seduction. Newton Abbot, England: David & Charles.  .  Seigel, Jessica (13 February 2004).. The New York Times. Retrieved 27 April 2018.  (1998). "Le Corset: A Material Culture Analysis of a Deluxe French Book". The Yale Journal of Criticism. 11 (1): 29–38. :.  .   ———  (2001). The Corset: A Cultural History. New Haven, Connecticut: Yale University Press.  .  (1996). The Breast Book: The Essential Guide to Breast Care & Breast Health for Women of All Ages. New York: DK Publishing.  978-0-7894-0420-6.  Summers, Leigh (2001). Bound to Please: A History of the Victorian Corset. Oxford: Berg.  .  Warner, Lucien T. (1948). Always Starting Things: Through 75 Eventful Years. Bridgeport, Connecticut: Warner Brothers.  .  Yu, W.; Fan, J.; Harlock, S. C.; Ng, S. P. (2006). Innovation and Technology of Women's Intimate Apparel. Boca Raton, Florida: CRC Press.  . 

External links[]


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