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Edip Ünal
Observed names:
E Unal,
E. Unal,
Edip UNAL,
Edip Unal,
Edip Unal³,
Unal E,
Unal, Edip
show all 7
Institution:
Dicle University
Observed institutions:
Dicle University,
Dokuz Eylül University,
Dicle Üniversitesi Hastaneleri,
Sağlık Bilimleri Üniversitesi,
Diyarbakır Gazi Yaşargil Eğitim ve Araştırma Hastanesi,
Kocaeli Üniversitesi
show all 6
ORCID:
0000-0002-9809-0977
Observed ORCID:
0000-0002-9809-0977
OpenAlex ID:
A5083441426
YIPF5 mutations cause neonatal diabetes and microcephaly through endoplasmic reticulum stress
2020
·
Elisa De Franco
, Maria Lytrivi
, et al.
·
Journal of Clinical Investigation
·
93
PDF
Frequency of Celiac Disease and Spontaneous Normalization Rate of Celiac Serology in Children and Adolescent Patients with Type 1 Diabetes
2020
·
Edip Unal
, Meliha Demiral
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
56
PDF
GLI1 inactivation is associated with developmental phenotypes overlapping with Ellis–van Creveld syndrome
2017
·
Adrian Palencia-Campos
, Asmat Ullah
, et al.
·
Human Molecular Genetics
·
54
PDF
Association of Subclinical Hypothyroidism with Dyslipidemia and Increased Carotid Intima-Media Thickness in Children
2016
·
Edip Unal
, Alper Akın
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
46
PDF
Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency
2021
·
Melek Yildiz
, Emregul Isik
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
45
PDF
Evaluation of QT dispersion and Tp‐e interval in children with subclinical hypothyroidism
2018
·
Alper Akın
, Edip Unal
, et al.
·
Pacing and Clinical Electrophysiology
·
29
17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort
2024
·
Zeynep Siklar
, Emine Camtosun
, et al.
·
Endocrine
·
26
PDF
A novel variant inLCHGRgene in 3 siblings with type 1 Leydig cell hypoplasia
2020
·
Amine Aktar Karakaya
, Edip Unal
, et al.
·
Gynecological Endocrinology
·
25
Validity of Six Month L-Thyroxine Dose for Differentiation of Transient or Permanent Congenital Hypothyroidism
2020
·
Muhammet Asena
, Meliha Demiral
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
25
PDF
Aromatase Deficiency due to a Novel Mutation in CYP19A1 Gene
2018
·
Edip Ünal
, Ruken Yıldırım
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
22
PDF
A novel mutation of AMHR2 in two siblings with persistent Müllerian duct syndrome
2018
·
Edip Unal
, Yusuf Kenan Haspolat
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
21
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets
2019
·
Zeynep Şıklar
, Serap Turan
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
19
PDF
Management of Thyrotoxicosis in Children and Adolescents: A Turkish Multi-center Experience
2018
·
Ihsan Esen
, Elvan Bayramoğlu
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
18
PDF
Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations
2020
·
Huseyin Demirbilek
, Atilla Cayir
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
17
PDF
Molecular Diagnosis of Monogenic Diabetes and Clinical/Laboratory Features in Turkish Children
2021
·
Damla Gökşen
, Ediz Yeşilkaya
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
15
PDF
Evaluation of the novel coronavirus disease in Turkish children: Preliminary outcomes
2020
·
kamil YILMAZ
, Ayfer Gozu Pirinccioglu
, et al.
·
Pediatric Pulmonology
·
14
PDF
Cytochrome P450 oxidoreductase deficiency caused by a novel mutation in the POR gene in two siblings: case report and literature review
2020
·
Edip Unal
, Meliha Demiral
, et al.
·
HORMONES
·
12
A rare cause of neonatal hypoglycemia in two siblings: TBX19 gene mutation
2018
·
Edip Unal
, Ruken Yıldırım
, et al.
·
HORMONES
·
12
A rare cause of delayed puberty and primary amenorrhea: 17α-hydroxylase enzyme deficiency
2021
·
Aslı Beştaş
, Semih Bolu
, et al.
·
Endocrine
·
11
Ectopic Posterior Pituitary, Polydactyly, Midfacial Hypoplasia and Multiple Pituitary Hormone Deficiency due to a Novel Heterozygous IVS11-2A>C(c.1957-2A>C) Mutation in the GLI2 Gene
2019
·
Meliha Demiral
, Hüseyin Demirbilek
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
11
PDF
Left and right ventricular functions may be impaired in children diagnosed with subclinical hypothyroidism
2020
·
Alper Akın
, Edip Unal
, et al.
·
Scientific Reports
·
9
PDF
A Different Perspective of Elevated Lactate in Pediatric Patients With Diabetic Ketoacidosis.
2020
·
E Unal
, A G Pirinccioglu
, et al.
·
PubMed
·
9
Clinical Characteristics of 46,XX Males with Congenital Adrenal Hyperplasia
2020
·
Şenay Savaş-Erdeve
, Zehra Aycan
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
8
PDF
Variant characterisation and clinical profile in a large cohort of patients with Ellis-van Creveld syndrome and a family with Weyers acrofacial dysostosis
2024
·
Umut Altunoglu
, Adrian Palencia-Campos
, et al.
·
Journal of Medical Genetics
·
7
PDF
The clinical and laboratory features of patients with triple A syndrome: a single-center experience in Turkey
2022
·
Ruken Yıldırım
, Edip Unal
, et al.
·
Endocrine
·
7
PDF
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Works count:
88
Citation count:
718
H-index:
15
I10-index:
20
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