Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ayşe Çiğdem AKTUĞLU ZEYBEK"'
Autor:
Tuğçe Uçar, Mehmet Şerif Cansever, Esra Isat, Tanyel Zubarioğlu, Ayşe Çiğdem Aktuğlu Zeybek, Birol Topçu, Nurhan Seyahi, Ertuğrul Kıykım
Publikováno v:
Balkan Medical Journal, Vol 41, Iss 2, Pp 113-120 (2024)
Background: Fabry disease is characterized by the accumulation of globotriaosylceramide. Substrate accumulation in lysosomes is thought to trigger an inflammatory response and is responsible for progressive organ damage through the induction of autoi
Externí odkaz:
https://doaj.org/article/6e1cc7cc23c746899aabeb3684aa9b24
Autor:
Mehmet Şerif CANSEVER, Zeynep KALAYCIOĞLU, Tanyel ZÜBARİOĞLU, Ertuğrul KIYKIM, Ayşe Çiğdem AKTUĞLU ZEYBEK, Fatma Bedia ERİM
Publikováno v:
Namık Kemal Tıp Dergisi, Vol 8, Iss 2, Pp 264-270 (2020)
Aim:L-2-hydroxyglutaric aciduria (L2HGA) which is autosomal recessive and characterized by psychomotor retardation, cerebellar ataxia, variable macrocephaly, and epilepsy is a rarely seen neurometabolic disease. The disease is biochemically identifie
Externí odkaz:
https://doaj.org/article/c78fee3bec314140a965fb1edd6c0d1d
Autor:
Ayşe Çiğdem, Aktuğlu Zeybek, Ertuğrul, Kıykım, Kenan, Barut, Tanyel, Zübarioğlu, Mehmet Şerif, Cansever, Özgür, Kasapçopur
Publikováno v:
Turkish Journal of Medical Sciences. 52:724-729
Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in childhood and manifests mainly as autoinflammation of the joints and other tissues. Several treatment options such as nonsteroidal antiinflammatory drugs, methotrexate, and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5052bedce6cd830dc6a8e9b59d145a38
https://doi.org/10.55730/1300-0144.5366
https://doi.org/10.55730/1300-0144.5366
Autor:
Yalçın Erdoğan, Ayşe Çiğdem Aktuğlu Zeybek, Mehmet Burak Dal, Ertugrul Kiykim, Necdet Güler, Altan Alim, Koray Acarli
Publikováno v:
Turkiye Klinikleri Journal of Pediatrics. 30:138-144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd4f04a4017242a4d0cc89c040dbf55b
https://doi.org/10.5336/pediatr.2020-76150
https://doi.org/10.5336/pediatr.2020-76150
Autor:
Ertugrul Kiykim, Ayşe Çiğdem Aktuğlu Zeybek, Tanyel Zübarioğlu, Mehmet Serif Cansever, Sezgin Sahin, Amra Adrovic, Kenan Barut, Ozgur Kasapcopur
Publikováno v:
Arch Rheumatol
Objectives This study aims to determine the prevalence of Fabry disease (FD) among patients with juvenile systemic lupus erythematosus (SLE). Patients and methods This cross-sectional study included 76 juvenile SLE patients (12 males; 64 females; mea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b93134f1671dc9dcccd1fdf10fcdc0c0
https://europepmc.org/articles/PMC7322306/
https://europepmc.org/articles/PMC7322306/
Autor:
Ayşe Çiğdem Aktuğlu Zeybek, Gozde Yesil, Tanyel Zübarioğlu, Cengiz Yalcinkaya, Ertugrul Kiykim, Ece Oge Enver, Alper Gezdirici, Cigdem Oruc, Mehmet Serif Cansever
Publikováno v:
Türk Pediatri Arşivi.
Aim L-2-hydroxyglutaric aciduria is a slowly progressive neurometabolic disorder caused by an enzymatic deficiency of L-2-hydroxyglutarate dehydrogenase. Here, we aimed to evaluate the clinical, neuroradiologic, and genotypic characteristics of patie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08ebe10b77f6940ba333ea48b47f30fe
https://doi.org/10.14744/turkpediatriars.2019.06926
https://doi.org/10.14744/turkpediatriars.2019.06926
Autor:
Tanyel, Zübarioğlu, İnci Pınar, Bilen, Ertugrul, Kıykım, Beyza Belde, Doğan, Ece Öge, Enver, Mehmet Şerif, Cansever, Ayşe Çiğdem Aktuğlu, Zeybek
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
The primary purpose of the present study is to evaluate the effect of chenodeoxycholic acid treatment on skeletal system findings in patients with cerebrotendinous xanthomatosis.This retrospective study was conducted between June 2013 and December 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1bfd043fac87d1528143885ea7ad6036
https://pubmed.ncbi.nlm.nih.gov/31384146
https://pubmed.ncbi.nlm.nih.gov/31384146
Long-term N-carbamylglutamate treatment of hyperammonemia in patients with classic organic acidemias
Autor:
Ertugrul Kiykim, Ozge Oguz, Cisem Duman, Tanyel Zubarioglu, Mehmet Serif Cansever, Ayse Cigdem Aktuglu Zeybek
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 26, Iss , Pp 100715- (2021)
Background: Classic organic acidurias (OAs) usually characterized by recurrent episodes of acidemia, ketonuria, and hyperammonemia leading to coma and even death if left untreated. Acute hyperammonemia episodes can be treated effectively with N-carba
Externí odkaz:
https://doaj.org/article/72b178e8a17447feb49364cb13920588