Academic literature on the topic 'Barraquer -Simons Syndrome'

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Journal articles on the topic "Barraquer -Simons Syndrome"

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Small, Juan E., Yasir N. Jassam, Kirstin M. Small, et al. "Barraquer-Simons Syndrome." American Journal of the Medical Sciences 352, no. 3 (2016): 280–84. http://dx.doi.org/10.1016/j.amjms.2016.05.007.

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Mansouri Hattab, N., S. Lahmiti, S. Aimadeddine, S. Fawzi, M. El Bouihi, and T. Fikry. "Syndrome de Barraquer-Simons." Revue de Stomatologie et de Chirurgie Maxillo-faciale 112, no. 3 (2011): 172–73. http://dx.doi.org/10.1016/j.stomax.2011.03.005.

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Bellon, N., F. Lioté, M. Bagot, E. Bourrat, and A. Petit. "Syndrome de Barraquer-Simons." Annales de Dermatologie et de Vénéréologie 140, no. 12 (2013): S603. http://dx.doi.org/10.1016/j.annder.2013.09.545.

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Dutta, Mita, Munira Afroz Siddika, Mohammad Aminul Islam, and Hurjahan Banu. "Barraquer–Simons syndrome: A case report." Bangabandhu Sheikh Mujib Medical University Journal 18, no. 2 (2025): e78654. https://doi.org/10.3329/bsmmuj.v18i2.78654.

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Murakhovskaya, E. V., and N. T. Starkova. "To the diagnosis of Barraquer-Simons syndrome." Problems of Endocrinology 44, no. 3 (1998): 29–31. http://dx.doi.org/10.14341/probl199844329-31.

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Abstract:
Barraquer-Simons syndrome is a rare disease characterized by the disappearance of subcutaneous fat in the upper half of the body with normal or excessive deposition of fat in the lower half of the body. There are other terms that refer to this disease: Hollander-Simons syndrome, progressive lipodystrophy, partial lipodystrophy, paradoxical lipodystrophy, progressive segmental lipodystrophy, i.e. the name emphasizes the disappearance of fat in certain parts of the body.
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Sedova, Tatiana G., Vladimir D. Elkin, Marina Y. Kobernik, and Elena N. Borodina. "A clinical case of Barraquer-Simons syndrome." Almanac of Clinical Medicine 49, no. 8 (2021): 564–70. http://dx.doi.org/10.18786/2072-0505-2021-49-067.

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Barraquer-Simons syndrome (SBS) belongs to the groupof lipodystrophy with complex etiology and pathophysiology and is characterized by progressive loss of subcutaneous fat, presumably related to autoimmune destruction of adipocytes. SBS is frequently associated with autoimmune disorders. Its first signs are found in childhood or puberty. It is characterized by gradual onset from the face with subsequent extension of the pathological process downwards without the involvement of the lower extremities. At the same time, there is a clear delimitation between the lipodystrophic and unaffected zones
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Tuzun, Binnur, Deniz Kircuval, Cuyan Demirkesen, Nadir Goksugur, Gaye Unal, and Yalcin Tuzun. "Barraquer-Simons syndrome with benign infundibulocystic proliferation." International Journal of Dermatology 42, no. 3 (2003): 210–12. http://dx.doi.org/10.1046/j.1365-4362.2003.01172.x.

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Requena Caballero, Celia, Miguel Ángel Navarro Mira, Isabel Febrer Bosch, José Miguel Fortea Bauxauli, and Adolfo Aliaga Boniche. "Barraquer-Simons lipodystrophy associated with antiphospholipid syndrome." Journal of the American Academy of Dermatology 49, no. 4 (2003): 768–69. http://dx.doi.org/10.1067/s0190-9622(03)00789-8.

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Simsek-Kiper, Pelin Ozlem, Emir Roach, Gulen Eda Utine, and Koray Boduroglu. "Barraquer-Simons syndrome: A rare clinical entity." American Journal of Medical Genetics Part A 164, no. 7 (2014): 1756–60. http://dx.doi.org/10.1002/ajmg.a.36491.

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Ferrarini, A., D. Milani, M. Bottigelli, G. Cagnoli, and Angelo Selicorni. "Two new cases of Barraquer-Simons syndrome." American Journal of Medical Genetics 126A, no. 4 (2004): 427–29. http://dx.doi.org/10.1002/ajmg.a.20623.

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Dissertations / Theses on the topic "Barraquer -Simons Syndrome"

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QUEZEL-GUERRAZ, JEROME. "Le syndrome de Barraquier-Simons : à propos de deux cas." Toulouse 3, 1989. http://www.theses.fr/1989TOU31221.

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Book chapters on the topic "Barraquer -Simons Syndrome"

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"Barraquer-Simons syndrome." In Dermatology Therapy. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/3-540-29668-9_342.

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