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Yuksel, Bilgin
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1

Plasma pentraxin‐3 levels and its role in childhood obesity..:

Uysal, Merve ; Mete, Burak ; Kara, Ertan...
Clinical Endocrinology.  101 (2024)  1 - p. 13-22 , 2024
Link: https://doi.org/10.1111/..
 
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2

17α Hydroxylase/17,20 lyase deficiency: clinical features a..:

Siklar, Zeynep ; Camtosun, Emine ; Bolu, Semih...
Endocrine.  , 2024
Link: https://doi.org/10.1007/..
 
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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/..
 
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4

The utility of annual growth velocity standard deviation sc..:

Ozdemir Dilek, Semine ; Turan, Ihsan ; Gurbuz, Fatih..
Hormones.  21 (2022)  3 - p. 391-397 , 2022
Link: https://doi.org/10.1007/..
 
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5

PLXNB1 mutations in the etiology of idiopathic hypogonadotr..:

Welch, Bradley A. ; Cho, Hyun‐ju ; Ucakturk, Seyit Ahmet...
Journal of Neuroendocrinology.  34 (2022)  4 - p. , 2022
Link: https://doi.org/10.1111/..
 
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6

A novel homozygous nonsense NDNF variant in Kallmann syndro..:

Kotan, Leman Damla ; Yildiz, Melek ; Turan, Ihsan...
American Journal of Medical Genetics Part A.  191 (2022)  3 - p. 831-834 , 2022
Link: https://doi.org/10.1002/..
 
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7

Inactivating NHLH2 variants cause idiopathic hypogonadotrop..:

Topaloglu, A. Kemal ; Simsek, Enver ; Kocher, Matthew A....
Human Genetics.  141 (2022)  2 - p. 295-304 , 2022
Link: https://doi.org/10.1007/..
 
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8

Loss-of-function variants in SEMA3F and PLXNA3 encoding sem..:

Kotan, Leman Damla ; Ternier, Gaetan ; Cakir, Aydilek Dagdeviren...
Genetics in Medicine.  23 (2021)  6 - p. 1008-1016 , 2021
Link: https://doi.org/10.1038/..
 
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9

Short stature and insulin-like growth Factor-I in neurofibr..:

Ucar, Habibe ; Altunbasak, Sakir ; Incecik, Faruk...
Annals of Medical Research.  28 (2021)  9 - p. 1763 , 2021
Link: https://doi.org/10.5455/..
 
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10

Clinical Characteristics and Long-term Follow-up of Patient..:

Demirbilek, Huseyin ; Cayir, Atilla ; Flanagan, Sarah E...
The Journal of Clinical Endocrinology & Metabolism.  105 (2020)  12 - p. e4351-e4359 , 2020
Link: https://doi.org/10.1210/..
 
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11

21-Hydroxylase deficiency: Mutational spectrum and Genotype..:

Turan, Ihsan ; Tastan, Mehmet ; Boga, Duygu D....
European Journal of Medical Genetics.  63 (2020)  4 - p. 103782 , 2020
Link: https://doi.org/10.1016/..
 
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12

Prevalence and associated phenotypes of PLXNA1 variants in ..:

Kotan, Leman D. ; Isik, Emregul ; Turan, Ihsan...
Clinical Genetics.  95 (2018)  2 - p. 320-324 , 2018
Link: https://doi.org/10.1111/..
 
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13

Molecular genetic studies in a case series of isolated hypo..:

Turan, Ihsan ; Kotan, Leman Damla ; Tastan, Mehmet...
Clinical Endocrinology.  88 (2018)  6 - p. 799-805 , 2018
Link: https://doi.org/10.1111/..
 
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14

Predicted Benign and Synonymous Variants in CYP11A1 Cause P..:

Maharaj, Avinaash ; Buonocore, Federica ; Meimaridou, Eirini...
Journal of the Endocrine Society.  3 (2018)  1 - p. 201-221 , 2018
Link: https://doi.org/10.1210/..
 
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15

The Authors' Reply: In systemic pseudohypoaldosteronism typ..:

Turan, Ihsan ; Topaloglu, Ali Kemal ; Yuksel, Bilgin
Clinical Endocrinology.  89 (2018)  2 - p. 241-242 , 2018
Link: https://doi.org/10.1111/..
 
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