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Selim Kurtoglu

Showing results (141-150 of 150) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|February 26, 2014
Neonatal diabetes in an infant of diabetic mother: same novel INS missense mutation in the mother and her offspringMehmet Adnan Ozturk, Selim Kurtoglu, Osman Bastug, et al.
Pediatrics and Neonatology|September 28, 2014
Investigation on malondialdehyde, S100B, and advanced oxidation protein product levels in significant hyperbilirubinemia and the effect of intensive phototherapy on these parametersDilek Sarici, Tamer Gunes, Cevat Yazici, et al.
European Journal of Medical Genetics|June 9, 2024
Congenital Adrenal Hyperplasia with Combined 21-hydroxylase deficiency and 17α-hydroxylase/17,20-lyase deficiency: An undervirilized maleLeyla Kara, Dilek Cicek, Ulku Gul Siraz, et al.
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University|December 22, 2017
Evaluation of aortic intima-media thickness in newborns with Down syndromeDilek Sarici, Selim Kurtoglu, Serdar Umit Sarici, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 18, 2008
Reference body mass index curves for Turkish children 6 to 18 years of ageAhmet Ozturk, Mumtaz M Mazicioglu, Nihal Hatipoglu, et al.
International Journal for Vitamin and Nutrition Research. Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Journal International De Vitaminologie Et De Nutrition|June 5, 2019
Effects of Lycopene in Hyperoxia-Induced Lung Injury in Newborn RatsOsman Bastug, Mehmet Fatih Sonmez, Mehmet Adnan Ozturk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesisHakan Cangul, Zehra Aycan, Halil Saglam, et al.
The Journal of Clinical Endocrinology and Metabolism|March 12, 2016
The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter StudyZeynep Atay, Ediz Yesilkaya, Senay Savas Erdeve, et al.
Human Mutation|February 4, 2014
Expanding the mutational spectrum of CRLF1 in Crisponi/CISS1 syndromeRoberta Piras, Francesca Chiappe, Ilaria La Torraca, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiencyLeyla Akin, Karine Rizzoti, Louise C Gregory, et al.
Pageof 15

Showing results (141-150 of 150) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 150 results.
Journal of Pediatric Endocrinology & Metabolism : JPEM|February 26, 2014
Neonatal diabetes in an infant of diabetic mother: same novel INS missense mutation in the mother and her offspringMehmet Adnan Ozturk, Selim Kurtoglu, Osman Bastug, et al.
Pediatrics and Neonatology|September 28, 2014
Investigation on malondialdehyde, S100B, and advanced oxidation protein product levels in significant hyperbilirubinemia and the effect of intensive phototherapy on these parametersDilek Sarici, Tamer Gunes, Cevat Yazici, et al.
European Journal of Medical Genetics|June 9, 2024
Congenital Adrenal Hyperplasia with Combined 21-hydroxylase deficiency and 17α-hydroxylase/17,20-lyase deficiency: An undervirilized maleLeyla Kara, Dilek Cicek, Ulku Gul Siraz, et al.
Advances in Clinical and Experimental Medicine : Official Organ Wroclaw Medical University|December 22, 2017
Evaluation of aortic intima-media thickness in newborns with Down syndromeDilek Sarici, Selim Kurtoglu, Serdar Umit Sarici, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 18, 2008
Reference body mass index curves for Turkish children 6 to 18 years of ageAhmet Ozturk, Mumtaz M Mazicioglu, Nihal Hatipoglu, et al.
International Journal for Vitamin and Nutrition Research. Internationale Zeitschrift Fur Vitamin- Und Ernahrungsforschung. Journal International De Vitaminologie Et De Nutrition|June 5, 2019
Effects of Lycopene in Hyperoxia-Induced Lung Injury in Newborn RatsOsman Bastug, Mehmet Fatih Sonmez, Mehmet Adnan Ozturk, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesisHakan Cangul, Zehra Aycan, Halil Saglam, et al.
The Journal of Clinical Endocrinology and Metabolism|March 12, 2016
The Etiology and Clinical Features of Non-CAH Gonadotropin-Independent Precocious Puberty: A Multicenter StudyZeynep Atay, Ediz Yesilkaya, Senay Savas Erdeve, et al.
Human Mutation|February 4, 2014
Expanding the mutational spectrum of CRLF1 in Crisponi/CISS1 syndromeRoberta Piras, Francesca Chiappe, Ilaria La Torraca, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiencyLeyla Akin, Karine Rizzoti, Louise C Gregory, et al.
Pageof 15