Academician profile · PROFESÖR
SERDAR CEYLANER
- Ana Dal Sağlık Bilimleri Temel Alanı
- Yan Dal Tıbbi Genetik
- TIP FAKÜLTESİ
- DAHİLİ TIP BİLİMLERİ BÖLÜMÜ
Scopus (SJR)
Q1
22
Q2
48
Q3
20
Q4
2
WoS (JCR)
Q1
10
Q2
15
Q3
29
Q4
38
TR Index
19
articles
Articles
- 2022 Vitamin D receptor gene polymorphisms in pediatric patients with leukemia-lymphoma: Does it have an impact on malignancy?
- 2018 Siblings with Ethylmalonic Encephalopathy: Case Report
- 2018 A 6-Month-Old Boy with Reddish, Scaly Skin: Netherton Syndrome
- 2018 “Double Hit” Homozygous Mutations for Two Different Rare Inborn Errors of Metabolism: A Burden for Countries with High Prevalences of Consangineous Marriages
- 2018 Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty
- 2017 A novel mutation in the desmoplakin gene in two female siblings with a rare form of dilated cardiomyopathy: Carvajal syndrome
- 2017 Impaired glucose tolerance in fanconi-bickel syndrome: eight patients with two novel mutations
- 2017 Delayed Diagnosis of a 17-Hydroxylase/17,20-Lyase Deficient Patient Presenting as a 46,XY Female: A Low Normal Potassium Level Can Be an Alerting Diagnostic Sign
- 2017 Microcephaly and developmental delay caused by short-chain acyl-coa dehydrogenase deficiency
- 2017 Beta-ketothiolase deficiency: an unusual cause of recurrent ketoacidosis
- 2017 An infant with glutaric aciduria type iic diagnosed with a novel mutation
- 2017 A Mutation in INSR in a Child Presenting with Severe Acanthosis Nigricans
- 2017 P.val452ile mutation of the slc25a13 gene in a turkish patient with citrin deficiency
- 2016 Genotypic and phenotypic features of the cystinosis patients from the south eastern part of turkey
- 2016 A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek Population
- 2015 Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene
- 2013 Primary Adrenal Insufficiency Caused by a Novel Mutation in DAX1 Gene
- 2013 A child with L-2 hydroxyglutaric aciduria presenting with dilated cardiomyopathy: Coincidence or a new syndrome?
- 2008 Autosomal dominant inheritance of congenital dislocation of the hip in 16 members of a family