Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Ali, Islek"'
Publikováno v:
Eurasian Journal of Medicine, Vol 54, Iss 2, Pp 173-180 (2022)
Externí odkaz:
https://doaj.org/article/0ca52dca143e4ec284bce1c2367c3c0e
Autor:
Cigdem Yuce Kahraman, Ali Islek, Abdulgani Tatar, Özlem Özdemir, Adil Mardinglu, Hasan Turkez
Publikováno v:
Medicina, Vol 57, Iss 2, p 123 (2021)
Wilson disease (WD) (OMIM# 277900) is an autosomal recessive inherited disorder characterized by excess copper (Cu) storage in different human tissues, such as the brain, liver, and the corneas of the eyes. It is a rare disorder that occurs in approx
Externí odkaz:
https://doaj.org/article/4017bb8324694f1b9f03c64ac1977852
Publikováno v:
Medicine Science, Vol 6, Iss 3, Pp 557-9 (2017)
The incidence of pancreatitis in children and adolescents has increased in recent years. The etiology of pancreatitis is more diverse in children compared to adults. Pancreatitis may present as acute pancreatitis, recurrent acute pancreatitis or chro
Externí odkaz:
https://doaj.org/article/2cccf33fa2fa433d8fe0caab5e985016
Autor:
Ali Islek, Gokhan Tumgor
Publikováno v:
World Journal of Hepatology
Although various complex definitions of acute-on-chronic liver failure (ACLF) have been suggested in relation to adult patients, there is currently no universal definition of the syndrome in pediatric patients. In simplified terms, ACLF is characteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c86ba03c1ef6738421bbe7c33f5c8be
http://europepmc.org/articles/PMC8568578
http://europepmc.org/articles/PMC8568578
Publikováno v:
Experimental and Clinical Transplantation. 19:686-692
Objectives Acute-on-chronic liver failure and its outcomes have not yet been evaluated in detail in children. We aimed to evaluate the etiology, acute events, and prognostic factors of acute-on-chronic liver failure in children. Materials and methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d12aff53089b337beb077a9ec1eec29a
https://doi.org/10.6002/ect.2020.0264
https://doi.org/10.6002/ect.2020.0264
Autor:
Ömer Faruk Beşer, Ayca Kiykim, Ali Islek, Serdar Nepesov, Gokhan Baysoy, Elif Karakoc-Aydiner, Sezin Aydemir, Yöntem Yaman, Haluk Cokugras, Bernice Lo, Yasemin Kendir Demirkol, Safa Baris, Satanay Hubrack, Fügen Çullu Çokuğraş, Ahmet Ozen
Publikováno v:
Journal of Clinical Immunology. 41:1406-1410
To the Editor: FCH And Mu Domain Containing Endocytic Adaptor 1 (FCHO1) gene encodes a protein that plays a critical role in clathrin-mediated endocytosis, a biological process that maintains cellular functions in signaling, nutrient- and growth fact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::567d8f10960dce77ea7682b64e613444
https://doi.org/10.1007/s10875-021-01042-2
https://doi.org/10.1007/s10875-021-01042-2
Autor:
Asena Pinar Sefer, Salim Can, Alper Bulutoğlu, Dilek Başer, Ali Islek, Derya Ufuk Altintaş, Safa Baris, Elif Karakoç. Aydiner, Bernice Lo, Ahmet Ozen
Publikováno v:
Clinical Immunology. 250:109587
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac792abaf153ef92bdadd1dbcce28a25
https://doi.org/10.1016/j.clim.2023.109587
https://doi.org/10.1016/j.clim.2023.109587
Autor:
Ali Islek, Gokhan Tumgor
Publikováno v:
World journal of gastrointestinal pharmacology and therapeutics. 13(4)
Biliary atresia (BA) and choledochal cysts are diseases of the intrahepatic and extrahepatic biliary tree. While their exact etiopathogeneses are not known, they should be treated promptly due to the potential for irreversible parenchymal liver disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d8e3902729c9aa60f91b74724720e81
https://pubmed.ncbi.nlm.nih.gov/36051179
https://pubmed.ncbi.nlm.nih.gov/36051179
Autor:
Ersin Sayar, Salih Kalay, Aygen Yilmaz, Osman Oztekin, Ali Islek, Gulsum Ozlem Elpek, Zuhal Kalay, Gonul Tezel, Reha Artan
Publikováno v:
American Journal of Perinatology Reports, Vol 04, Iss 02, Pp e61-e64 (2014)
Abstract Microvillus inclusion disease is one of the congenital diarrheal disorders characterized by the appearance of inclusion bodies on the intestinal epithelium. To date there are a few cases and also a few other associated finding reports relate
Externí odkaz:
https://doaj.org/article/afcb5fd6e9664001a094126bfc90b8bb
Publikováno v:
Acta gastro-enterologica Belgica. 84(2)
Background: Seronegative autoimmune hepatitis (AIH) is a diagnostic challenge with unclear prognosis. This study describes the features and outcomes of seronegative AIH in children. Patients and methods: Patients under 18 years of age, who had been d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::846ff09fdff0a5715fb02eac2f1f44de
https://pubmed.ncbi.nlm.nih.gov/34217180
https://pubmed.ncbi.nlm.nih.gov/34217180