Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Senol Citli"'
Autor:
Nadir Koçak, Şenol Çitli
Publikováno v:
Journal of Contemporary Medicine, Vol 12, Iss 5, Pp 804-810 (2022)
Background: Familial Mediterranean Fever (FMF) is an autoinflammatory disease and may express as various clinical findings. Chemokines are crucial elements of the inflammatory process. MCP-1 and its’ receptor CCR2 are the main chemokines for monocy
Externí odkaz:
https://doaj.org/article/81f5efb18e55438382130e2d45248af9
Publikováno v:
Journal of Contemporary Medicine, Vol 11, Iss 4, Pp 494-499 (2021)
Introduction: In the pathogenesis of the FMF disease, cytokines play important roles in the inflammation of the serous membranes. This study aims to investigate the relationship between serum levels of IL-1β, IL-18 and caspase-1 with CRP, ESR, fibri
Externí odkaz:
https://doaj.org/article/03782e1403114921921a2c84e7c12f26
Publikováno v:
Journal of Contemporary Medicine, Vol 11, Iss 4, Pp 494-499 (2021)
Introduction: In the pathogenesis of the FMF disease, cytokines play important roles in the inflammation of the serous membranes. This study aims to investigate the relationship between serum levels of IL-1β, IL-18 and caspase-1 with CRP, ESR, fibri
Externí odkaz:
https://doaj.org/article/6905c7b03e1f4ba0adc08f5e800c526d
Autor:
Ulas Emre Akbulut, Hamdi Cihan Emeksiz, Senol Citli, Alper Han Cebi, Hatice Ayca Ata Korkmaz, Gaye Baki
Publikováno v:
Jornal de Pediatria (Versão em Português), Vol 95, Iss 3, Pp 350-357 (2019)
Objective: The prevalence of non‐alcoholic fatty liver disease in children has risen significantly, owing to the worldwide childhood obesity epidemic in the last two decades. Non‐alcoholic fatty liver disease is closely linked to sedentary lifest
Externí odkaz:
https://doaj.org/article/0b459b0678bc4cd5a382db90406b42e8
Autor:
Ahmet Cevdet Ceylan, Senol Citli, Haktan Bagis Erdem, Ibrahim Sahin, Elif Acar Arslan, Murat Erdogan
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)
Abstract Background Chromosomal microarray analysis is a first-stage test that is used for the diagnosis of intellectual disability and global developmental delay. Chromosomal microarray analysis can detect well-known microdeletion syndromes. It also
Externí odkaz:
https://doaj.org/article/b8828a53ac01469e9274f04ea1d966f7
Publikováno v:
Brain and Development. 45:300-305
Autor:
Senol Citli
Balanced chromosomal re-arrangements (BCR) are re-arrangements with no loss or gain of genetic material and usually not associated with clinical abnormalities. However, BCR carriers may have children with a chromosomal anomaly as a result of an unbal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52e87ee2b9fdb81b89bbffc7a7d981a7
Autor:
Senol Citli, Esra Serdaroglu
Introduction: Complex cortical dysplasia with other brain malformations-7 (a.k.a. polymicrogyria) caused by mutations in TUBB2B gene is a clinically heterogeneous condition. Case report: We report two siblings with polymicrogyria. Brain MRI showed po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d266fac04a91cb9e39450f162f04864
https://avesis.gazi.edu.tr/publication/details/867f740c-1328-4ad6-aff6-12fe2ac3a8dd/oai
https://avesis.gazi.edu.tr/publication/details/867f740c-1328-4ad6-aff6-12fe2ac3a8dd/oai
Autor:
Ibrahim Sahin, Ahmet Cevdet Ceylan, Haktan Bağış Erdem, Murat Erdogan, Elif Acar Arslan, Senol Citli
Publikováno v:
Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-9 (2018)
Background Chromosomal microarray analysis is a first-stage test that is used for the diagnosis of intellectual disability and global developmental delay. Chromosomal microarray analysis can detect well-known microdeletion syndromes. It also contribu