İndolamin 2, 3-Dioksijenaz Gen Polimorfizminin Behçet Hastalığı ve Kliniği Üzerine Etkisi
Ü Uçar - 2022 - search.proquest.com
İNDOLAMİN 2, 3 DİOKSİJENAZ GEN POLİMORFİZMİNİN BEHÇET HASTALIĞI VE KLİNİĞİ
ÜZERİNE ETKİSİ Page 1 TC BURSA ULUDAĞ ÜNİVERSİTESİ TIP FAKÜLTESİ SAĞLIK …
ÜZERİNE ETKİSİ Page 1 TC BURSA ULUDAĞ ÜNİVERSİTESİ TIP FAKÜLTESİ SAĞLIK …
[PDF][PDF] Familial vitiligo in mother and child; the genetic theory connection
MM Oripelaye, OA Olasode, O Onayemi… - Our Dermatology …, 2017 - academia.edu
Vitiligo is an acquired loss of skin pigment of unknown etiology. It frequently occurs in
familial clusters thereby favoring the genetic theory for its pathogenesis. Several genes have …
familial clusters thereby favoring the genetic theory for its pathogenesis. Several genes have …
Hematopoietic Stem Cell Transplantation for BehÇet's Syndrome
LL do Prado, L Piron-Ruiz, M Ruiz… - … and Cellular Therapies …, 2021 - taylorfrancis.com
Behçet's syndrome is a multifactorial, autoinflammatory, chronic variable vessel vasculitis of
unknown etiology characterized by recurrent oral and genital lesions, and internal organs …
unknown etiology characterized by recurrent oral and genital lesions, and internal organs …
1. Epidemiology of Adamantiades-Behçet's
CC ZOUBOULIS - 1994 - books.google.com
Adamantiades-Behçet's disease is a universal disorder with varying prevalence, ie 80–370
pat/100,000 inhabitants in Turkey, 2–30 in the Asian continent and 0.1–7.5 in Europe and …
pat/100,000 inhabitants in Turkey, 2–30 in the Asian continent and 0.1–7.5 in Europe and …
Enfermedad de Behcet
AMT Giraldo, LFP Peñaranda, CJV Franco… - Revista Colombiana de …, 2009 - Elsevier
La enfermedad de Behcet (EB) es una enfermedad multisistémica de causa desconocida,
caracterizada por un curso crónico, recurrente y compromiso inflamatorio de los vasos de …
caracterizada por un curso crónico, recurrente y compromiso inflamatorio de los vasos de …
[PDF][PDF] Aphtes, aphtose buccale récidivante et maladie de Behçet
JP Coulon, E Piette - Encycl Méd Chir, 1999 - researchgate.net
Dans ce chapitre, seront successivement envisagés les aphtes simples, isolés, l'aphtose
buccale récidivante (ABR) et le syndrome de Behçet, véritable maladie générale [8]. De nos …
buccale récidivante (ABR) et le syndrome de Behçet, véritable maladie générale [8]. De nos …
[PDF][PDF] ĠSTANBUL TIP FAKÜLTESĠ DERĠ VE ZÜHREVĠ HASTALIKLARI ANABĠLĠM DALINDA TAKĠPLĠ BEHÇET HASTALIĞI, BĠPOLAR AFTÖZĠS …
MSH JHAĠSH, AA KÖSE - nek.istanbul.edu.tr
Tezimin hazırlanmasında, her aĢamada bana yol gösteren, yapıcı öneri ve eleĢtirileri ile
katkıda bulunan, yakın ilgi ve yardımlarını esirgemeyen tez danıĢmanım, Sayın Prof. Dr. Afet …
katkıda bulunan, yakın ilgi ve yardımlarını esirgemeyen tez danıĢmanım, Sayın Prof. Dr. Afet …
Behçet Syndrome in Children
E Seyahi, I Koné-Paut - Behçet Syndrome, 2020 - Springer
Behçet syndrome (BS) may be occasionally seen in children; its frequency ranges between
4 and 26% among the whole BS population. Genders are equally affected, and familial …
4 and 26% among the whole BS population. Genders are equally affected, and familial …
[HTML][HTML] Behçet's Disease: An Enigmatic Malady with Plethoric Expressions
S Mohamed, AR Krishnan - Different Aspects of Behçet's Disease, 2019 - intechopen.com
Behçet's disease (BD) is a chronic, inflammatory, repetitive, debilitating systemic vasculitis
with conglomerate system involvement of uncharted aetiology portrayed by the triad of oral …
with conglomerate system involvement of uncharted aetiology portrayed by the triad of oral …