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Fatih Gurbuz

Showing results (1-10 of 35) with videos related to

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American Journal of Medical Genetics. Part A|January 3, 2025
Hajdu-Cheney Syndrome, a Rare Cause of Acro-Osteolysis and Osteoporosis With Zoledronic Acid ExperienceGonul Buyukyilmaz, Mehmet Adiguzel, Fatih Gurbuz, et al.
Hormones (Athens, Greece)|March 4, 2022
The utility of annual growth velocity standard deviation scores and measurements of biochemical parameters in long-term treatment monitoring of children with 21-hydroxylase deficiencySemine Ozdemir Dilek, Ihsan Turan, Fatih Gurbuz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 26, 2014
The effect of lifestyle change and metformin therapy on serum arylesterase and paraoxonase activity in obese childrenAtilla Çayır, Mehmet İbrahim Turan, Fatih Gurbuz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 29, 2016
Sertoli cell only syndrome with ambiguous genitaliaFatih Gurbuz, Serdar Ceylaner, Seyda Erdogan, et al.
Indian Journal of Pediatrics|September 6, 2013
Etiological evaluation of patients presenting with isolated micropenis to an academic health care centerTugba Bilmez Aslan, Fatih Gurbuz, Fatih Temiz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 22, 2023
Body mass index evolution and ovarian function in adolescent girls who received GnRH agonist treatment for central precocious puberty or early and fast pubertyGonul Buyukyilmaz, Serkan Bilge Koca, Keziban Toksoy Adiguzel, et al.
Clinical Endocrinology|March 28, 2018
Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistanceIhsan Turan, Leman Damla Kotan, Mehmet Tastan, et al.
European Journal of Pediatrics|April 13, 2026
Menarche timing after GnRHa treatment in cases of central precocious puberty or early and fast pubertyDuygu Deligozoglu, Gonul Buyukyilmaz, Irem Gokdemir, et al.
Molecular Syndromology|June 11, 2026
CHOPS Syndrome: A Rare Malformation Syndrome with de novo AFF4 Gene VariantIrem Gokdemir, Sirmen Kizilcan Cetin, Esra Kilic, et al.
European Journal of Medical Genetics|October 6, 2019
21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplificationIhsan Turan, Mehmet Tastan, Duygu D Boga, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics. Part A|January 3, 2025
Hajdu-Cheney Syndrome, a Rare Cause of Acro-Osteolysis and Osteoporosis With Zoledronic Acid ExperienceGonul Buyukyilmaz, Mehmet Adiguzel, Fatih Gurbuz, et al.
Hormones (Athens, Greece)|March 4, 2022
The utility of annual growth velocity standard deviation scores and measurements of biochemical parameters in long-term treatment monitoring of children with 21-hydroxylase deficiencySemine Ozdemir Dilek, Ihsan Turan, Fatih Gurbuz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 26, 2014
The effect of lifestyle change and metformin therapy on serum arylesterase and paraoxonase activity in obese childrenAtilla Çayır, Mehmet İbrahim Turan, Fatih Gurbuz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 29, 2016
Sertoli cell only syndrome with ambiguous genitaliaFatih Gurbuz, Serdar Ceylaner, Seyda Erdogan, et al.
Indian Journal of Pediatrics|September 6, 2013
Etiological evaluation of patients presenting with isolated micropenis to an academic health care centerTugba Bilmez Aslan, Fatih Gurbuz, Fatih Temiz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 22, 2023
Body mass index evolution and ovarian function in adolescent girls who received GnRH agonist treatment for central precocious puberty or early and fast pubertyGonul Buyukyilmaz, Serkan Bilge Koca, Keziban Toksoy Adiguzel, et al.
Clinical Endocrinology|March 28, 2018
Molecular genetic studies in a case series of isolated hypoaldosteronism due to biosynthesis defects or aldosterone resistanceIhsan Turan, Leman Damla Kotan, Mehmet Tastan, et al.
European Journal of Pediatrics|April 13, 2026
Menarche timing after GnRHa treatment in cases of central precocious puberty or early and fast pubertyDuygu Deligozoglu, Gonul Buyukyilmaz, Irem Gokdemir, et al.
Molecular Syndromology|June 11, 2026
CHOPS Syndrome: A Rare Malformation Syndrome with de novo AFF4 Gene VariantIrem Gokdemir, Sirmen Kizilcan Cetin, Esra Kilic, et al.
European Journal of Medical Genetics|October 6, 2019
21-Hydroxylase deficiency: Mutational spectrum and Genotype-Phenotype relations analyses by next-generation sequencing and multiplex ligation-dependent probe amplificationIhsan Turan, Mehmet Tastan, Duygu D Boga, et al.
Pageof 4