Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ece Oge‐Enver"'
Autor:
Tanyel Zubarioglu, Harika Oyku Dinc, Duhan Hopurcuoglu, Ruveyda Gulmez, Esma Uygur, Gizem Yilmaz, Saffa Ahmadzada, Gozde Uzunyayla-Inci, Ece Oge-Enver, Ertugrul Kiykim, Bekir Kocazeybek, Cigdem Aktuglu-Zeybek
Publikováno v:
Frontiers in Immunology, Vol 13 (2023)
IntroductionSARS-CoV-2 infection can lead to a life-threatening acute metabolic decompensation in children with inborn errors of metabolism (IEM), so vaccination is mandatory. However, IEMs can also impair innate or adaptive immunity, and the impact
Externí odkaz:
https://doaj.org/article/d3691e481b3b4379a8ce328ecf93fabc
Autor:
Gulin Sunter, Ece Oge Enver, Azad Akbarzade, Serap Turan, Pinar Vatansever, Dilek Ince Gunal, Goncagul Haklar, Abdullah Bereket, Kadriye Agan, Tulay Guran
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Congenital sphingosine-1-phosphate (S1P) lyase deficiency due to biallelic mutations in SGPL1 gene has recently been described in association with primary adrenal insufficiency and steroid-resistant nephrotic syndrome. S1P lyase,
Externí odkaz:
https://doaj.org/article/bd219541ea214e42ad4d4ea3ea85a112
Autor:
Esra Isat, Ece Oge-Enver, Esma Uygur, Saffa Ahmadzada, Tanyel Zubarioglu, Cigdem Aktuglu-Zeybek, Ertugrul Kiykim, Mehmet Serif Cansever, Duhan Hopurcuoglu
Publikováno v:
Telemedicine and e-Health. 28:258-265
Background: The prognosis of phenylketonuria (PKU) in terms of neurocognitive outcome is directly related to lifelong phenylalanine (Phe) levels and adherence to treatment. Monitoring and treatment of PKU patients can be complicated in challenging ci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1045154ceec8c37692023306f157dfb0
https://doi.org/10.1089/tmj.2020.0569
https://doi.org/10.1089/tmj.2020.0569
Autor:
Tanyel Zubarioglu, Sinem Oral‐Cebeci, Duhan Hopurcuoglu, Esma Uygur, Saffa Ahmadzada, Gözde Uzunyayla‐Inci, Ece Oge‐Enver, Sedanur Akca, Mirsaid Aghalarov, Gizem Yilmaz, Ertugrul Kiykim, Cigdem Aktuglu‐Zeybek
Publikováno v:
Journal of paediatrics and child health.
There are no recommended guidelines or clinical studies on safety of COVID-19 vaccines in patients with inborn errors of metabolism (IEMs). Here, we aimed to examine the relationship between COVID-19 vaccination and metabolic outcome in paediatric IE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38b73aeda3f20c863b9d5facb15def88
https://pubmed.ncbi.nlm.nih.gov/36173142
https://pubmed.ncbi.nlm.nih.gov/36173142
Autor:
Didem Tezen, Cigdem Aktuglu Zeybek, Ertugrul Kiykim, Aysegul Gunduz, Ece Oge Enver, Meral E. Kiziltan
Publikováno v:
Parkinsonism & Related Disorders. 80:12-14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f6037368926f227e2a711d7dd30e7c9
https://doi.org/10.1016/j.parkreldis.2020.09.002
https://doi.org/10.1016/j.parkreldis.2020.09.002
Autor:
Ece Oge Enver, Goncagül Haklar, Pinar Vatansever, Abdullah Bereket, Tulay Guran, Leyla Bilgin, Perran Boran, Omer Guran, Serap Turan
Publikováno v:
Pediatric research. 92(1)
BACKGROUND Interpretation of the results of steroid hormone measurements is challenging at early infancy. The liquid chromatography-tandem mass spectrometry (LC-MS/MS) method provides a powerful tool for diagnosing steroidogenesis disorders. We aimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7583ec9774367884359ea3753bdfd19e
https://pubmed.ncbi.nlm.nih.gov/34556810
https://pubmed.ncbi.nlm.nih.gov/34556810
Autor:
Tanyel Zubarioglu, Seffa Ahmadzada, Duhan Hopurcuoglu, Ece Oge Enver, Ayse Cigdem Aktuglu Zeybek, Ertugrul Kiykim
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 34(1)
Objectives There has been a recent worldwide outbreak of coronavirus disease (COVID-19). Most of the health system capacity has been directed to COVID-19 patients, and routine outpatient clinics have been suspended. Chronic disease patients, such as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a9c9470de88039d9bf07fd2c1532dc0
https://pubmed.ncbi.nlm.nih.gov/33185576
https://pubmed.ncbi.nlm.nih.gov/33185576
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:
Ayse Cigdem Aktuglu Zeybek, İnci Pınar Bilen, Ertugrul Kiykim, Ece Oge Enver, Tanyel Zubarioglu, Beyza Belde Doğan, Mehmet Serif Cansever
Publikováno v:
Türk Pediatri Arşivi.
Aim 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. Material and methods This retrospective study was conducted between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22bf25b766a71aa7324b6640f4374080
https://doi.org/10.14744/turkpediatriars.2019.23281
https://doi.org/10.14744/turkpediatriars.2019.23281
Autor:
Tulay Guran, Ece Oge Enver, Abdullah Bereket, Serap Turan, Dilek Ince Gunal, Goncagül Haklar, Kadriye Agan, Gulin Sunter, Pinar Vatansever, Azad Akbarzade
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-6 (2018)
BMC Neurology
BMC Neurology
Background Congenital sphingosine-1-phosphate (S1P) lyase deficiency due to biallelic mutations in SGPL1 gene has recently been described in association with primary adrenal insufficiency and steroid-resistant nephrotic syndrome. S1P lyase, on the ot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c40eaaf3e1ac80f254394cc77c401499
https://doi.org/10.1186/s12883-018-1049-9
https://doi.org/10.1186/s12883-018-1049-9