Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Hande KÜÇÜK KURTULGAN"'
Autor:
Nurullah Çelik, Hande Küçük Kurtulgan, Fatih Kılıçbay, Gaffari Tunç, Ayça Kömürlüoğlu, Onur Taşçı, Cemile Ece Çağlar Şimşek, Taha Çınar, Yeşim Sıdar Duman
Publikováno v:
JCRPE, Vol 14, Iss 4, Pp 469-474 (2022)
The genetic cause of 46, XY disorder of sex development (DSD) still cannot be determined in about half of the cases. GATA-4 haploinsufficiency is one of the rare causes of DSD in genetic males (46, XY). Twenty-two cases with 46, XY DSD due to GATA-4
Externí odkaz:
https://doaj.org/article/6262eb38c6b84ebeac9a5a6b0758d61f
Publikováno v:
Journal of Pediatric Research, Vol 9, Iss 2, Pp 132-137 (2022)
Aim:Atopy is associated with a genetic predisposition to develop allergic diseases such as allergic rhinitis, asthma, and atopic dermatitis. In this study, we aimed to compare the prevalence of Familial Mediterranean Fever (FMF) mutations in asthma a
Externí odkaz:
https://doaj.org/article/264c570d284642b5b23b6dba9f4d37a8
Autor:
Hande Küçük Kurtulgan, Emine Elif Altuntaş, Malik Ejder Yıldırım, Öztürk Özdemir, Binnur Bağcı, İlhan Sezgin
Publikováno v:
Journal of International Advanced Otology, Vol 15, Iss 3, Pp 373-378 (2019)
Externí odkaz:
https://doaj.org/article/3253458e0f814d6c8a0254a155f030a1
Autor:
Taha Çınar, Cemile Ece Çağlar Şimşek, Hande Küçük Kurtulgan, Ayça Kömürlüoğlu, Onur Taşcı, Fatih Kılıçbay, Yeşim Sıdar Duman, Gaffari Tunç, Nurullah Çelik
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 14:469-474
The genetic cause of 46, XY Disorder of Sex Development(DSD) still cannot be determined in about half of the cases. GATA-4 haploinsufficiency is one of the rare causes of DSD in genetic males (46, XY). Twenty-two cases with 46, XY DSD due to GATA-4 h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51c242ff6a50a2b93987c660948766ab
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0112
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0112
Publikováno v:
Turkiye Klinikleri Journal of Case Reports. 29:230-233
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1adeec67c96b34a6380ad3960c3e353
https://doi.org/10.5336/caserep.2021-83838
https://doi.org/10.5336/caserep.2021-83838
Autor:
Malik Ejder Yildirim, Gokhan Bagci, Mansur Kayataş, Hande Küçük Kurtulgan, Meryem Timucin, Ilhan Sezgin, Burak Baser, Suleyman Koz
Publikováno v:
Turkish Journal of Nephrology. 29:304-309
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c77cededbe4705966fc094039991f48
https://doi.org/10.5152/turkjnephrol.2020.4300
https://doi.org/10.5152/turkjnephrol.2020.4300
Autor:
Hasan Kilicgun, Malik Ejder Yildirim, Ilhan Sezgin, Hande Küçük Kurtulgan, Öztürk Özdemir, Burak Baser, Didem S. Aydemir
Publikováno v:
Annals of Saudi Medicine
Annals of Saudi Medicine, Vol 39, Iss 6, Pp 382-387 (2019)
Annals of Saudi Medicine, Vol 39, Iss 6, Pp 382-387 (2019)
BACKGROUND: Familial Mediterranean fever (FMF), an autosomal recessive, autoinflammatory disease that is common in Arabs, Jews, Armenians and Turks, is caused by mutations in the MEFV gene, which encodes a protein called pyrin. The disease is charact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b72d7073f8d05422c4c28358a69bd0c5
https://doi.org/10.5144/0256-4947.2019.382
https://doi.org/10.5144/0256-4947.2019.382
Publikováno v:
Volume: 10, Issue: 1 232-237
ENT Updates
ENT Updates (2020)
ENT Updates
ENT Updates (2020)
Objective: Chronic otitis media (COM) is a multifactorial disorder, the pathogenesis of which has yet to be fully elucidated. Numerous aetiological factors, including genetics, eustachian tube dysfunction, autoimmunity, infection, osteoclastic activi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a2ca7287a867bc3c64358ca27b9cb49
https://dergipark.org.tr/tr/pub/entupdates/issue/53920/594272
https://dergipark.org.tr/tr/pub/entupdates/issue/53920/594272
Publikováno v:
Journal of gynecology obstetrics and human reproduction. 48(7)
Objective Chromosomal abnormalities are more common in the first trimester abortions. We aimed to investigate the types and prevalence of chromosomal abnormalities in couples with recurrent first trimester miscarriages in Sivas, Turkey. Materials and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::917d23c82bf014cfa64521179dda38d7
https://pubmed.ncbi.nlm.nih.gov/31085277
https://pubmed.ncbi.nlm.nih.gov/31085277
Publikováno v:
Journal of Clinical and Analytical Medicine (2019)
WOS: 000451875800022
Aim: Matrix metalloproteinases (MMPs) may influence many biological and pathological processes including inflammatory responses. Thrombospondins (TSP) are a glycoprotein group of the extracellular matrix. In this study, we a
Aim: Matrix metalloproteinases (MMPs) may influence many biological and pathological processes including inflammatory responses. Thrombospondins (TSP) are a glycoprotein group of the extracellular matrix. In this study, we a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87c2af79c58ba736ad474b43859c2e29
https://www.bayrakol.org/tr/2019/january2019/original-article-2019/item/2034-a-possible-interaction-of-timp-1-and-tsp-1-with-familial-mediterranean-fever
https://www.bayrakol.org/tr/2019/january2019/original-article-2019/item/2034-a-possible-interaction-of-timp-1-and-tsp-1-with-familial-mediterranean-fever