Zobrazeno 1 - 10
of 1 331
pro vyhledávání: '"JUNCTIONAL EPIDERMOLYSIS BULLOSA"'
Publikováno v:
Indian Dermatology Online Journal, Vol 15, Iss 5, Pp 834-836 (2024)
Epidermolysis bullosa (EB) is a heterogeneous group of genetic disorders characterized by the formation of blisters either spontaneously or at the sites of trauma. These heal with post-inflammatory hypopigmentation, scarring, or milia formation. We h
Externí odkaz:
https://doaj.org/article/f52fb9b3de854230ac0a60e1b64aba6c
Autor:
May El Hachem, Andrea Diociaiuti, Giovanna Zambruno, Tonia Samela, Francesca Ferretti, Claudia Carnevale, Renata Linertová, Christine Bodemer, Dédée F. Murrell, Damiano Abeni
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-10 (2024)
Abstract Background Inherited epidermolysis bullosa (EB) is a clinically and genetically heterogeneous group of skin fragility disorders characterized by blister formation following minor trauma. Four major types are distinguished based on the level
Externí odkaz:
https://doaj.org/article/021ea3190f5a49efb5f6f7aefcca65e4
Autor:
Lily Hertel, BS, Mollie Hutton, MS, Paul Bogner, MD, Raminder Grover, MD, Drew Kuraitis, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 46, Iss , Pp 11-14 (2024)
Externí odkaz:
https://doaj.org/article/0adb8c7046bb459a96b87aac0e4cdd9f
Autor:
Kazufumi Yoshida, Soshi Yoshida, Yoshimasa Hori, Hideki Tsubota, Ryosuke Mochizuki, Tohru Nagano, Tadaaki Koyama
Publikováno v:
Journal of Cardiothoracic Surgery, Vol 19, Iss 1, Pp 1-6 (2024)
Abstract Background Junctional epidermolysis bullosa is a rare skin and mucosal disorder characterized by blister formation in response to minor trauma and extracutaneous manifestations. There have been no reports of cardiac surgery and prognosticati
Externí odkaz:
https://doaj.org/article/5ca37815c62e4e76be21069466b54be2
Publikováno v:
Journal of Plastic and Reconstructive Surgery, Vol 2, Iss 4, Pp 156-162 (2023)
Epidermolysis bullosa is a group of inherited skin fragility disorders with blister formation in the basement membrane zone. Chronic scarring after repeated blistering of the hands causes narrowing of the first web, flexion contractures of the digits
Externí odkaz:
https://doaj.org/article/b4905d21ce9442bf999e0526f40366bb
Publikováno v:
Vestnik Dermatologii i Venerologii, Vol 98, Iss 6, Pp 17-38 (2023)
Junctional epidermolysis bullosa most commonly results from mutations in the LAMA3, LAMB3, LAMC2, COL17A1, ITGA6 and ITGB4 genes. Junctional epidermolysis bullosa is characterized by clinical heterogeneity. To date, scientific findings allow to evalu
Externí odkaz:
https://doaj.org/article/1be20f00f6d241e8a75f9fecfa633c06
Publikováno v:
Journal of South Asian Association of Pediatric Dentistry, Vol 5, Iss 3, Pp 176-179 (2022)
Epidermolysis bullosa (EB) is a group of hereditary disorders characterized by the mechanical fragility of skin and the appearance of blisters, bullae, and ulcers. This case report presents a 10-year-old boy with junctional EB (JEB) diagnosed at 2 mo
Externí odkaz:
https://doaj.org/article/ce26bebc46874f1ab8f4e4a44ac703b8
Autor:
Widhiati S, Dewi ST, Yefta, Danarti R, Soebono H, Irmawati YE, Puspitasari M, Trisnowati N, Wibawa T, Purnomosari D, Wirohadidjojo YW
Publikováno v:
Clinical, Cosmetic and Investigational Dermatology, Vol Volume 15, Pp 2197-2202 (2022)
Suci Widhiati,1,2 Shinta Trilaksmi Dewi,3 Yefta,3 Retno Danarti,3 Hardyanto Soebono,3 Yulia Eka Irmawati,3 Monika Puspitasari,3 Niken Trisnowati,3 Tri Wibawa,4 Dewajani Purnomosari,5 Yohanes Widodo Wirohadidjojo3 1Department of Dermatology and Venere
Externí odkaz:
https://doaj.org/article/0f667ed3819743509872f992c59a0130
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