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Murat Öcal
Observed name:
Murat ÖCAL
Institution:
Pamukkale University
Observed institutions:
Sağlık Bilimleri Üniversitesi,
Diyarbakır Gazi Yaşargil Eğitim ve Araştırma Hastanesi,
Pamukkale University
ORCID:
0000-0001-7190-075X
Observed ORCID:
0000-0001-7190-075X
OpenAlex ID:
A5102795119
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
Testicular Adrenal Rest Tumors in Patients with Congenital Adrenal Hyperplasia: A Case Series
2020
·
Didem Yildirimçakar
, Selda Ayça Altincik
, et al.
·
Trends in Pediatrics
·
19
PDF
Capillary Bedside Blood Glucose Measurement in Neonates: Missing a Diagnosis of Galactosemia
2015
·
Mehmet Nuri Özbek
, Murat Öcal
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
6
PDF
Hyperchloremia and Prolonged Acidosis During Treatment for Pediatric Diabetic Ketoacidosis
2024
·
Didem Yıldırımçakar
, Murat Öcal
, et al.
·
Pediatric Emergency Care
·
5
Could MOTS-C Levels in Children with Type 1 Diabetes Mellitus Be an İndicator for Early Diabetic Kidney Disease?
2024
·
İlknur Girisgen
, Selda Ayça Altıncık
, et al.
·
Journal of Clinical Research in Pediatric Endocrinology
·
4
PDF
Incidence of Autoimmune Thyroid Disease in Patients with Type 1 Diabetes
2020
·
Edip Unal
, Meliha Demiral
, et al.
·
Güncel Pediatri
·
1
Evaluation of the Epidemiological, Presenting and Follow-up Characteristics and their Impacts on the Glycemic Control in a Large Cohort of Pediatric Type 1 Diabetes Mellitus Patients from Southeastern Anatolian Region of Turkey
2016
·
Mehmet Nuri Özbek
, Hüseyin Demirbilek
, et al.
·
55th ESPE Meeting
·
1
Transient neonatal diabetes mellitus
2023
·
Gülay SÖNMEZ DEMİR
, Didem YILDIRIM ÇAKAR
, et al.
·
Pamukkale Medical Journal
PDF
Tip 1 Diyabetli Hastalarda Otoimmün Tiroid Hastaliği Sıklığı
2020
·
Edip Ünal
, Meliha Demiral
, et al.
·
Güncel Pediatri
PDF
Kallmann Syndrome Due to a Homozygous Missense c.217C>T (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene
2016
·
Mehmet Nuri Ozturk
, Hüseyin Demirbilek
, et al.
·
55th ESPE Meeting
Presenting Characteristics, Auxological, and Aetiologic Evaluation of 364 Patients with GH Deficiency
2015
·
Mehmet Nuri Özbek
, Birsen Baysal
, et al.
·
54th Annual ESPE
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Works count:
11
Citation count:
61
H-index:
4
I10-index:
2
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