Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Murat Durdu"'
Autor:
Dilek Bayramgürler, Abdullah Demirbaş, Murat Durdu, Göktuğ Aslankoç, Tuğrul Eruyar, Cüyan Demirkesen
Publikováno v:
Dermatology Practical & Conceptual, Vol 14, Iss 2 (2024)
Externí odkaz:
https://doaj.org/article/8d5945ac2c494f9c92088895592c81c7
Autor:
Asude Kara Polat, Mehmet Kamil Mülayim, Tuğba Falay Gür, Ayda Acar, Burçin Cansu Bozca, Can Ceylan, Fadime Kılınç, Rukiye Yasak Güner, Hülya Albayrak, Murat Durdu, Ayşe Esra Koku Aksu, Fatma Nalbant, Ekin Şavk, Dilek Bayramgürler, Munise Daye, Ralfi Singer, Emine Tuğba Alataş, Vefa Aslı Erdemir, Mehmet Salih Gürel, Soner Uzun, Savaş Yaylı
Publikováno v:
Dermatology Practical & Conceptual, Vol 14, Iss 2 (2024)
Introduction: Pemphigus vulgaris (PV) is an autoimmune disease that mostly affects the oral mucosa. Objectives: This study aimed to determine the demographic, clinical and treatment characteristics as well as the quality of life of patients with P
Externí odkaz:
https://doaj.org/article/0da095482aab48ba9e51610151a87008
Publikováno v:
Dermatology Practical & Conceptual, Vol 13, Iss 3 (2023)
Externí odkaz:
https://doaj.org/article/d0c23f1303524051b4c079bdabb00e6a
Publikováno v:
Lipids in Health and Disease, Vol 18, Iss 1, Pp 1-6 (2019)
Abstract Background Chanarin Dorfman Syndrome (CDS) is a rare autosomal recessive disorder characterized by the multisytemic accumulation of neutral lipids inside the cytoplasmic lipid droplets. This condition is caused by mutations in the abhydrolas
Externí odkaz:
https://doaj.org/article/a13e6b28d1bb4119abece008a752de3f
Publikováno v:
European Journal of Translational Myology (2021)
ABHD5 protein is widely involved in lipid and energy homeostasis. Mutations in the ABHD5 gene are associated with the onset of Neutral Lipid Storage Disease with Ichthyosis (NLSDI), historically known as Chanarin Dorfman Syndrome (CDS). CDS is a rare
Externí odkaz:
https://doaj.org/article/3c3c50d297c74c2a8d91fd5ee1d908aa
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)
Abstract Background Chanarin Dorfman Syndrome (CDS) is a rare autosomal recessive disorder characterized by ichthyosiform non-bullous erythroderma and variable involvement of the liver and the neuromuscular system. In CDS patients, the accumulation o
Externí odkaz:
https://doaj.org/article/236a233c87c5425898d3c586e89125ea
Publikováno v:
Cukurova Medical Journal, Vol 43, Iss 1, Pp 227-230 (2018)
Piyoderma gangrenozum, hızlı bir şekilde geniş, ağrılı ve nekrotik ülserlere dönüşen kutanöz papülo-püstüller ile karakterize nadir bir inflamatuvar cilt hastalığıdır. Bu lezyonlar başlangıçta sıklıkla yara enfeksiyonu ve nekr
Externí odkaz:
https://doaj.org/article/b2f4dcb5ffc14e7085235b39cfc04b1e
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 3, Pp 1142-1143 (2019)
Externí odkaz:
https://doaj.org/article/b68f9d7890d946d58c6fa22807c2698b
Publikováno v:
Cukurova Medical Journal, Vol 40, Iss 3, Pp 614-618 (2015)
Chanarin Dorfman Sendromu multisistemik genetik geçişli metabolik hastalık olup konjenital iktiyozis ve çeşitli hücrelerde lipid depolanması ile ilişkilidir. İktiyozisli hastalarda periferik kan yaymasında nötrofillerde lipid vakuollerinin
Externí odkaz:
https://doaj.org/article/47b7dbce30234560aca0a76f8e8c9c38
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 40, Iss 3, Pp 614-618 (2015)
Chanarin Dorfman Syndrome is a multisystem inherited metabolic disorder associated with congenital ichthyosis and accumulation of lipid droplets in varios types of cells. Observation of lipid vacuoles in neutrophils (Jordan's anomaly) in peirpheral b
Externí odkaz:
https://doaj.org/article/1b15b0d578534600b718c52f32f67486