Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Tulay Guran

Showing results (21-30 of 128) with videos related to

Pageof 13
Sort By:
Clinical Dysmorphology|October 23, 2010
Radiologic and hormonal evaluation of pituitary abnormalities in patients with Bardet-Biedl syndromeTulay Guran, Gazanfer Ekinci, Zeynep Atay, et al.
Clinical Endocrinology|September 11, 2014
Reference values for serum dehydroepiandrosterone-sulphate in healthy children and adolescents with emphasis on the age of adrenarche and pubarcheTulay Guran, Irfan Firat, Feyza Yildiz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 20, 2025
Positive neonatal screening test for congenital adrenal hyperplasia in a case with 3β-Hydroxysteroid dehydrogenase type 2 deficiencyMerve Anik, Deniz Erdogan, Tugba Baris, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 19, 2011
Comparison of oral alendronate versus prednisolone in treatment of infants with vitamin D intoxicationRabia G Sezer, Tulay Guran, Cem Paketçi, et al.
American Journal of Medical Genetics. Part A|July 6, 2022
A homozygous Y443C variant in the RNPC3 is associated with severe syndromic congenital hypopituitarism and diffuse brain atrophyDiğdem Bezen, Orkide Kutlu, Stephane Mouilleron, et al.
Hormone Research in Paediatrics|March 27, 2023
An Overlooked Manifestation of Hypercortisolism: Cerebral Cortical Atrophy and Challenges in Identifying the Etiology of Hypercortisolism - A Report of 2 Pediatric CasesElif Eviz, Gul Yesiltepe Mutlu, Ayfer Arduc Akcay, et al.
Magnesium Research|April 15, 2011
Cognitive and psychosocial development in children with familial hypomagnesaemiaTulay Guran, Ayse Arman, Teoman Akcay, et al.
European Journal of Pediatrics|October 25, 2012
Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasiaBelma Haliloglu, Tulay Guran, Zeynep Atay, et al.
Hormone Research in Paediatrics|February 14, 2015
Premature pubarche, hyperinsulinemia and hypothyroxinemia: novel manifestations of congenital portosystemic shunts (Abernethy malformation) in childrenSerpil Bas, Tulay Guran, Zeynep Atay, et al.
European Journal of Endocrinology|November 11, 2008
Puberty in a case with novel 17-hydroxylase mutation and the putative role of estrogen in development of pubic hairSerap Turan, Abdullah Bereket, Tulay Guran, et al.
Pageof 13

Showing results (21-30 of 128) with videos related to

Sort By:
Pageof 13
Clinical Dysmorphology|October 23, 2010
Radiologic and hormonal evaluation of pituitary abnormalities in patients with Bardet-Biedl syndromeTulay Guran, Gazanfer Ekinci, Zeynep Atay, et al.
Clinical Endocrinology|September 11, 2014
Reference values for serum dehydroepiandrosterone-sulphate in healthy children and adolescents with emphasis on the age of adrenarche and pubarcheTulay Guran, Irfan Firat, Feyza Yildiz, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 20, 2025
Positive neonatal screening test for congenital adrenal hyperplasia in a case with 3β-Hydroxysteroid dehydrogenase type 2 deficiencyMerve Anik, Deniz Erdogan, Tugba Baris, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 19, 2011
Comparison of oral alendronate versus prednisolone in treatment of infants with vitamin D intoxicationRabia G Sezer, Tulay Guran, Cem Paketçi, et al.
American Journal of Medical Genetics. Part A|July 6, 2022
A homozygous Y443C variant in the RNPC3 is associated with severe syndromic congenital hypopituitarism and diffuse brain atrophyDiğdem Bezen, Orkide Kutlu, Stephane Mouilleron, et al.
Hormone Research in Paediatrics|March 27, 2023
An Overlooked Manifestation of Hypercortisolism: Cerebral Cortical Atrophy and Challenges in Identifying the Etiology of Hypercortisolism - A Report of 2 Pediatric CasesElif Eviz, Gul Yesiltepe Mutlu, Ayfer Arduc Akcay, et al.
Magnesium Research|April 15, 2011
Cognitive and psychosocial development in children with familial hypomagnesaemiaTulay Guran, Ayse Arman, Teoman Akcay, et al.
European Journal of Pediatrics|October 25, 2012
Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasiaBelma Haliloglu, Tulay Guran, Zeynep Atay, et al.
Hormone Research in Paediatrics|February 14, 2015
Premature pubarche, hyperinsulinemia and hypothyroxinemia: novel manifestations of congenital portosystemic shunts (Abernethy malformation) in childrenSerpil Bas, Tulay Guran, Zeynep Atay, et al.
European Journal of Endocrinology|November 11, 2008
Puberty in a case with novel 17-hydroxylase mutation and the putative role of estrogen in development of pubic hairSerap Turan, Abdullah Bereket, Tulay Guran, et al.
Pageof 13