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Catli, Gonul
134
results:
Search for persons
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Online (134)
Mediatypes
Articles (Online) (41)
OpenAccess-fulltext (93)
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english (117)
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1
Genetic Findings in Short Turkish Children Born to Consangu..:
Joustra, Sjoerd D.
;
Isik, Emregul
;
Wit, Jan M.
...
Hormone Research in Paediatrics. , 2024
Link:
https://doi.org/10.1159/..
?
2
Clinical features, diagnosis and treatment outcomes of Cush..:
Tarçın, Gürkan
;
Çatlı, Gönül
;
Çetinkaya, Semra
...
Clinical Endocrinology. 100 (2023) 1 - p. 19-28 , 2023
Link:
https://doi.org/10.1111/..
?
3
POU6F2 mutation in humans with pubertal failure alters GnRH..:
Cho, Hyun-Ju
;
Gurbuz, Fatih
;
Stamou, Maria
...
Frontiers in Endocrinology. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
4
Atypical STAT5B deficiency, severe short stature and mild i..:
Catli, Gonul
;
Gao, Wen
;
Foley, Corinne
...
Molecular and Cellular Endocrinology. 559 (2023) - p. 111799 , 2023
Link:
https://doi.org/10.1016/..
?
5
A childhood primary hyperparathyroidism due to parathyroid ..:
Bulut, Seyran
;
Filibeli, Berna
;
Manyas, Hayrullah
...
Pediatric Academic Case Reports. 1 (2022) 1 - p. 1-4 , 2022
Link:
https://doi.org/10.61107..
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6
Genotype of congenital adrenal hyperplasia patients with te..:
Aycan, Zehra
;
Keskin, Melikşah
;
Lafcı, Naz Güleray
...
European Journal of Medical Genetics. 65 (2022) 12 - p. 104654 , 2022
Link:
https://doi.org/10.1016/..
?
7
Does fludrocortisone treatment cause hypomagnesemia in chil..:
ERBAŞ, İbrahim Mert
;
ALTINCIK, Selda Ayça
;
ÇATLI, Gönül
...
TURKISH JOURNAL OF MEDICAL SCIENCES. 51 (2021) 1 - p. 231-237 , 2021
Link:
https://doi.org/10.3906/..
?
8
The relationship of carotid intima-media thickness with ant..:
TUHAN, Hale
;
ÖZTÜRK, Tülay
;
ÇATLI, Gönül
...
TURKISH JOURNAL OF MEDICAL SCIENCES. 51 (2021) 4 - p. 1738-1746 , 2021
Link:
https://doi.org/10.3906/..
?
9
Oxytocin receptor gene polymorphism and low serum oxytocin ..:
Çatli, Gönül
;
Acar, Sezer
;
Cingöz, Gülten
...
International Journal of Obesity. 45 (2021) 9 - p. 2064-2073 , 2021
Link:
https://doi.org/10.1038/..
?
10
Systematic genetic testing for recessively inherited monoge..:
Patel, Kashyap A.
;
Ozbek, Mehmet N.
;
Yildiz, Melek
...
Diabetologia. 65 (2021) 2 - p. 336-342 , 2021
Link:
https://doi.org/10.1007/..
?
11
Childhood-onset mild diabetes caused by a homozygous novel ..:
Filibeli, Berna Eroğlu
;
Çatli, Gönül
;
Ayranci, İlkay
...
Hormones. 21 (2021) 1 - p. 163-169 , 2021
Link:
https://doi.org/10.1007/..
?
12
Clinical and Hormonal Profiles Correlate With Molecular Cha..:
Yildiz, Melek
;
Isik, Emregul
;
Abali, Zehra Yavas
...
The Journal of Clinical Endocrinology & Metabolism. 106 (2021) 9 - p. e3714-e3724 , 2021
Link:
https://doi.org/10.1210/..
?
13
Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Defi..:
Guran, Tulay
;
Kara, Cengiz
;
Yildiz, Melek
...
The Journal of Clinical Endocrinology & Metabolism. 105 (2020) 4 - p. e1718-e1728 , 2020
Link:
https://doi.org/10.1210/..
?
14
Can ocular changes be detected early in children and adoles..:
Öztürk, Hakan
;
Özen, Bediz
;
Manyas, Hayrullah
..
International Ophthalmology. 40 (2020) 10 - p. 2503-2514 , 2020
Link:
https://doi.org/10.1007/..
?
15
Impaired systolic and diastolic left ventricular function i..:
Tuhan, Hale
;
Demircan, Tülay
;
Altıncık, Ayca
...
Cardiology in the Young. 29 (2019) 3 - p. 319-324 , 2019
Link:
https://doi.org/10.1017/..
1-15