Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Wafaa M. Ramadan"'
Publikováno v:
Journal of Dermatological Treatment, Vol 34, Iss 1 (2023)
Background: Hereditary hypotrichosis simplex is a rare genetic hair disease that affects the scalp. Failure to grow normal hair in terms of length and density is the main complaint of patients. Diagnosis usually established by exclusion of other cong
Externí odkaz:
https://doaj.org/article/e739b985adba436e88ee63158ef3c4d4
Publikováno v:
The Medical Journal of Cairo University. 87:1439-1448
Background: Vitiligo is an acquired pigmentary disorder of unknown etiology that affects up to 1% of the general population of all skin types.It is a multifactorial disorder. There are numerous medical and surgical treatments aimed at repigmentation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::816e6893be74bb269c3c899db59d4da5
https://doi.org/10.21608/mjcu.2019.53513
https://doi.org/10.21608/mjcu.2019.53513
Publikováno v:
Journal of the Egyptian Womenʼs Dermatologic Society. 15:158-164
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9b029579fd4781a685cf0aa1c48230e
https://doi.org/10.1097/01.ewx.0000541495.17892.bd
https://doi.org/10.1097/01.ewx.0000541495.17892.bd
Publikováno v:
Journal of the Egyptian Womenʼs Dermatologic Society. 14:128-136
Background Aquaporin-3 (AQP-3), an aquaglyceroporin, has recently been ascribed a potential role in cell proliferation, migration, and tumorigenesis. Objective The aims of this study was to determine the expression and localization of AQP-3 in normal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::988fdc97d2710de9eae360c468784273
https://doi.org/10.1097/01.ewx.0000513084.47849.72
https://doi.org/10.1097/01.ewx.0000513084.47849.72