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Korcan Demir

Showing results (91-100 of 136) with videos related to

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Journal of Clinical Research in Pediatric Endocrinology|February 13, 2024
Salivary Sex Steroid Levels in Infants and the Relation with Infantile ColicFulya Mete Kalaycı, Özlem Gürsoy Doruk, İbrahim Mert Erbaş, et al.
Life Science Alliance|November 24, 2021
MANF supports the inner hair cell synapse and the outer hair cell stereocilia bundle in the cochleaKuu Ikäheimo, Anni Herranen, Vilma Iivanainen, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 13, 2025
Concerns for mood disorders in children presenting with early menarche is not an indication for pubertal suppressionKübra Yüksek Acinikli, Ozge Besci, Gözde Akın Kağızmanlı, 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.
Hormones (Athens, Greece)|July 12, 2023
Which method is more effective in predicting adult height in pubertal girls treated with gonadotropin-releasing hormone agonist?Gözde Akın Kağızmanlı, Reyhan Deveci Sevim, Özge Besci, et al.
Clinical Endocrinology|September 30, 2014
Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated familiesHuseyin Demirbilek, M Nuri Ozbek, Korcan Demir, et al.
Hormones (Athens, Greece)|March 14, 2022
Atypical comorbidities in a child considered to have type 1 diabetes led to the diagnosis of SLC29A3 spectrum disorderÖzge Besci, Kashyap Amratlal Patel, Gizem Yıldız, et al.
Hormone Research in Paediatrics|September 24, 2014
Psychomotor retardation caused by a defective thyroid hormone transporter: report of two families with different MCT8 mutationsAhmet Anık, Simone Kersseboom, Korcan Demir, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 17, 2025
What is the Most Effective Method for Predicting Adult Height in Boys with Constitutional Delay of Growth and Puberty?Gözde Akın Kağızmanlı, Deniz Özalp Kızılay, Reyhan Deveci Sevim, 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.
Pageof 14

Showing results (91-100 of 136) with videos related to

Sort By:
Pageof 14
Journal of Clinical Research in Pediatric Endocrinology|February 13, 2024
Salivary Sex Steroid Levels in Infants and the Relation with Infantile ColicFulya Mete Kalaycı, Özlem Gürsoy Doruk, İbrahim Mert Erbaş, et al.
Life Science Alliance|November 24, 2021
MANF supports the inner hair cell synapse and the outer hair cell stereocilia bundle in the cochleaKuu Ikäheimo, Anni Herranen, Vilma Iivanainen, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 13, 2025
Concerns for mood disorders in children presenting with early menarche is not an indication for pubertal suppressionKübra Yüksek Acinikli, Ozge Besci, Gözde Akın Kağızmanlı, 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.
Hormones (Athens, Greece)|July 12, 2023
Which method is more effective in predicting adult height in pubertal girls treated with gonadotropin-releasing hormone agonist?Gözde Akın Kağızmanlı, Reyhan Deveci Sevim, Özge Besci, et al.
Clinical Endocrinology|September 30, 2014
Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated familiesHuseyin Demirbilek, M Nuri Ozbek, Korcan Demir, et al.
Hormones (Athens, Greece)|March 14, 2022
Atypical comorbidities in a child considered to have type 1 diabetes led to the diagnosis of SLC29A3 spectrum disorderÖzge Besci, Kashyap Amratlal Patel, Gizem Yıldız, et al.
Hormone Research in Paediatrics|September 24, 2014
Psychomotor retardation caused by a defective thyroid hormone transporter: report of two families with different MCT8 mutationsAhmet Anık, Simone Kersseboom, Korcan Demir, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 17, 2025
What is the Most Effective Method for Predicting Adult Height in Boys with Constitutional Delay of Growth and Puberty?Gözde Akın Kağızmanlı, Deniz Özalp Kızılay, Reyhan Deveci Sevim, 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.
Pageof 14