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1 . Academic Journal
Identification of a novel homozygous NR5A1 variant in a patient with a 46,XY disorders of sex development.
저자
by
Kırkgöz, Tarık
;
Gürsoy, Semra
;
Acar, Sezer
;
Köprülü, Özge
;
Özkaya, Beyhan
, et al.
소스
Journal of Pediatric Endocrinology & Metabolism; Jun2024, Vol. 37 Issue 6, p575-579, 5p
Full Text(De Gruyter)
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7 . Academic Journal
Primary adrenal insufficiency in children: Diagnosis and management
저자
by
Kirkgoz, Tarik
;
Guran, Tulay
.
소스
In
Best Practice & Research Clinical Endocrinology & Metabolism
August 2018 32(4):397-424
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4 . Periodical
Identification of a novel homozygous NR5A1variant in a patient with a 46,XY disorders of sex development
저자
by
Kırkgöz, Tarık
;
Gürsoy, Semra
;
Acar, Sezer
;
Köprülü, Özge
;
Özkaya, Beyhan
, et al.
소스
Journal of Pediatric Endocrinology & Metabolism; June 2024, Vol. 37 Issue: 6 p575-579, 5p
Full Text(De Gruyter)
Web of Science
Scopus
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7 . Academic Journal
Evaluation of Serum Advanced Glycation End Product Levels and Microvascular Complications in Children and Adolescents with Type 1 Diabetes Mellitus.
저자
by
Kırkgöz, Tarık
;
Acar, Sezer
;
Küme, Tuncay
;
Kırkgöz, Hatice Hilal
;
Tabanlı, Gülin
, et al.
소스
Turkish Archives of Pediatrics
. Jan2024, Vol. 59 Issue 1, p31-37. 7p.
Scopus
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7 . Academic Journal
Challenges in the Management of a 7-Year-Old Child with Thyrotropin-Secreting Pituitary Adenoma and the Review of the Literature.
저자
by
Kirkgoz, Tarik
;
Abali, Saygin
;
Seker, Askin
;
Gurpinar Tosun, Busra
;
Eltan, Mehmet
, et al.
소스
Hormone Research in Paediatrics
. 2023, Vol. 96 Issue 5, p527-537. 11p.
Web of Science
Scopus
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7 . Academic Journal
Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty
저자
by
Kırkgöz, Tarık
;
Kaygusuz, Sare Betül
;
Alavanda, Ceren
;
Helvacıoğlu, Didem
;
Abalı, Zehra Yavaş
, et al.
소스
Journal of Pediatric Endocrinology and Metabolism
. 36(4):401-408
Full Text(De Gruyter)
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7 . Periodical
Molecular analysis of MKRN3gene in Turkish girls with sporadic and familial idiopathic central precocious puberty
저자
by
Kırkgöz, Tarık
;
Kaygusuz, Sare Betül
;
Alavanda, Ceren
;
Helvacıoğlu, Didem
;
Abalı, Zehra Yavaş
, et al.
소스
Journal of Pediatric Endocrinology & Metabolism; April 2023, Vol. 36 Issue: 4 p401-408, 8p
Full Text(De Gruyter)
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7 . Academic Journal
Distinctively Different Phenotypes of Two Cases with a Rare Karyotype of 45,X/47,XYY Mosaicism: Case Report and Literature Review.
저자
by
Köprülü, Özge
;
Acar, Sezer
;
Erdoğan, Kadri Murat
;
Nalbantoğlu, Özlem
;
Kırkgöz, Tarık
, et al.
소스
Journal of Pediatric Research
. Dec2022, Vol. 9 Issue 4, p401-408. 8p.
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7 . Academic Journal
A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis.
저자
by
Kırkgöz, Tarık
;
Özkan, Behzat
;
Hazan, Filiz
;
Acar, Sezer
;
Nalbantoğlu, Özlem
, et al.
소스
Frontiers in Genetics; 6/24/2022, Vol. 13, p1-7, 7p
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7 . Academic Journal
Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features.
저자
by
Eltan, Mehmet
;
Yavas Abali, Zehra
;
Turkyilmaz, Ayberk
;
Gokce, Ibrahim
;
Abali, Saygın
, et al.
소스
Calcified Tissue International
. Apr2022, Vol. 110 Issue 4, p441-450. 10p.
Web of Science
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