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Sezer Acar

Showing results (31-40 of 48) with videos related to

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Frontiers in Genetics|July 11, 2022
A Null Mutation of <i>TNFRSF11A</i> Causes Dysosteosclerosis, Not OsteopetrosisTarık Kırkgöz, Behzat Özkan, Filiz Hazan, et al.
International Journal of Obesity (2005)|June 6, 2021
Oxytocin receptor gene polymorphism and low serum oxytocin level are associated with hyperphagia and obesity in adolescentsGönül Çatli, Sezer Acar, Gülten Cingöz, et al.
Turkish Journal of Medical Sciences|January 24, 2021
The relationship of carotid intima-media thickness with anthropometric and metabolic parameters in patients with classic congenital adrenal hyperplasiaHale Tuhan, Tülay Öztürk, Gönül Çatlı, et al.
The Turkish Journal of Pediatrics|October 27, 2020
A novel compound heterozygous variant in CYP19A1 resulting in aromatase deficiency with normal ovarian tissueSezer Acar, İbrahim Mert Erbaş, Ahu Paketçi, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|April 18, 2022
Hyperandrogenism correlates with psychological symptoms in adolescents with polycystic ovary syndromeZeynep Donbaloğlu, Hale Tuhan, Özge Gizli Çoban, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 15, 2025
Is oxytocin related to psychiatric symptoms in adolescents with obesity?Gonca Özyurt, Gönül Çatlı, Sezer Acar, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|September 27, 2019
NOVEL <i>VDR</i> MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATIONKorcan Demir, Minjing Zou, Roua A Al-Rijjal, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 18, 2018
Targeted next generation sequencing in patients with maturity-onset diabetes of the young (MODY)Taha R Özdemir, Özgür Kırbıyık, Bumin N Dündar, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 12, 2023
Atypical Presentation and Course of ACTH-independent Cushing's Syndrome in Two FamiliesKübra Yüksek Acinikli, Sezer Acar, Ahu Paketçi, et al.
Diabetes|January 27, 2021
Loss of MANF Causes Childhood-Onset Syndromic Diabetes Due to Increased Endoplasmic Reticulum StressHossam Montaser, Kashyap A Patel, Diego Balboa, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
Frontiers in Genetics|July 11, 2022
A Null Mutation of <i>TNFRSF11A</i> Causes Dysosteosclerosis, Not OsteopetrosisTarık Kırkgöz, Behzat Özkan, Filiz Hazan, et al.
International Journal of Obesity (2005)|June 6, 2021
Oxytocin receptor gene polymorphism and low serum oxytocin level are associated with hyperphagia and obesity in adolescentsGönül Çatli, Sezer Acar, Gülten Cingöz, et al.
Turkish Journal of Medical Sciences|January 24, 2021
The relationship of carotid intima-media thickness with anthropometric and metabolic parameters in patients with classic congenital adrenal hyperplasiaHale Tuhan, Tülay Öztürk, Gönül Çatlı, et al.
The Turkish Journal of Pediatrics|October 27, 2020
A novel compound heterozygous variant in CYP19A1 resulting in aromatase deficiency with normal ovarian tissueSezer Acar, İbrahim Mert Erbaş, Ahu Paketçi, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|April 18, 2022
Hyperandrogenism correlates with psychological symptoms in adolescents with polycystic ovary syndromeZeynep Donbaloğlu, Hale Tuhan, Özge Gizli Çoban, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 15, 2025
Is oxytocin related to psychiatric symptoms in adolescents with obesity?Gonca Özyurt, Gönül Çatlı, Sezer Acar, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|September 27, 2019
NOVEL <i>VDR</i> MUTATIONS IN PATIENTS WITH VITAMIN D-DEPENDENT RICKETS TYPE 2A: A MILD DISEASE PHENOTYPE CAUSED BY A NOVEL CANONICAL SPLICE-SITE MUTATIONKorcan Demir, Minjing Zou, Roua A Al-Rijjal, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 18, 2018
Targeted next generation sequencing in patients with maturity-onset diabetes of the young (MODY)Taha R Özdemir, Özgür Kırbıyık, Bumin N Dündar, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 12, 2023
Atypical Presentation and Course of ACTH-independent Cushing's Syndrome in Two FamiliesKübra Yüksek Acinikli, Sezer Acar, Ahu Paketçi, et al.
Diabetes|January 27, 2021
Loss of MANF Causes Childhood-Onset Syndromic Diabetes Due to Increased Endoplasmic Reticulum StressHossam Montaser, Kashyap A Patel, Diego Balboa, et al.
Pageof 5