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Erdal Eren

Showing results (51-60 of 84) with videos related to

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Journal of Clinical Research in Pediatric Endocrinology|August 22, 2020
Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in TurkeyYasemin Denkboy Öngen, Erdal Eren, Özgecan Demirbaş, et al.
The Journal of Molecular Diagnostics : JMD|July 18, 2024
Genotype and Phenotype Correlation of Patients with Osteogenesis ImperfectaLamiya Aliyeva, Yasemin Denkboy Ongen, Erdal Eren, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|November 12, 2025
Disrupted glutamate-gaba balance in children with adenoid hypertrophy:a targeted metabolomic and clinical correlation studyTuğba Yemiş, Medeni Arpa, Mehmet Birinci, et al.
Hormone Research in Paediatrics|December 23, 2014
GPR30 Gene Polymorphisms Are Associated with Gynecomastia Risk in AdolescentsHüseyin Anıl Korkmaz, Tuba Edgünlü, Erdal Eren, et al.
Gene|March 15, 2014
Genetic variants of estrogen beta and leptin receptors may cause gynecomastia in adolescentErdal Eren, Tuba Edgunlu, Huseyin Anil Korkmaz, et al.
Irish Journal of Medical Science|July 27, 2025
Genetic and clinical characteristics of children with mody: insights into novel HNF4A variants and genotype-phenotype correlationMeltem Buhur Pirimoglu, Ozge Beyza Gundogdu Ogutlu, Hatice Nursoy, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 27, 2014
An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesisHakan Cangul, Halil Saglam, Yaman Saglam, et al.
Global Medical Genetics|August 25, 2021
Psychomotor Delay in a Child with <i>FGFR3</i> G380R Pathogenic Mutation Causing AchondroplasiaMahmut C Ergoren, Erdal Eren, Elena Manara, et al.
Hormone Molecular Biology and Clinical Investigation|September 27, 2018
Effect of experimentally induced hypothyroidism during gestation period on activity dependent neurotrophic factor (ADNF) in newborn rat brain tissueGökhan Cesur, Mehtap Kılıç Eren, Erdal Eren, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 30, 2025
Impact of the Transition Council in Type 1 Diabetes: Bridging the Gap to Adult CareErhan Hocaoglu, Hatice Nursoy, Filiz Mercan Saridas, et al.
Pageof 9

Showing results (51-60 of 84) with videos related to

Sort By:
Pageof 9
Journal of Clinical Research in Pediatric Endocrinology|August 22, 2020
Genotype and Phenotype Heterogeneity in Neonatal Diabetes: A Single Centre Experience in TurkeyYasemin Denkboy Öngen, Erdal Eren, Özgecan Demirbaş, et al.
The Journal of Molecular Diagnostics : JMD|July 18, 2024
Genotype and Phenotype Correlation of Patients with Osteogenesis ImperfectaLamiya Aliyeva, Yasemin Denkboy Ongen, Erdal Eren, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|November 12, 2025
Disrupted glutamate-gaba balance in children with adenoid hypertrophy:a targeted metabolomic and clinical correlation studyTuğba Yemiş, Medeni Arpa, Mehmet Birinci, et al.
Hormone Research in Paediatrics|December 23, 2014
GPR30 Gene Polymorphisms Are Associated with Gynecomastia Risk in AdolescentsHüseyin Anıl Korkmaz, Tuba Edgünlü, Erdal Eren, et al.
Gene|March 15, 2014
Genetic variants of estrogen beta and leptin receptors may cause gynecomastia in adolescentErdal Eren, Tuba Edgunlu, Huseyin Anil Korkmaz, et al.
Irish Journal of Medical Science|July 27, 2025
Genetic and clinical characteristics of children with mody: insights into novel HNF4A variants and genotype-phenotype correlationMeltem Buhur Pirimoglu, Ozge Beyza Gundogdu Ogutlu, Hatice Nursoy, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 27, 2014
An essential splice site mutation (c.317+1G>A) in the TSHR gene leads to severe thyroid dysgenesisHakan Cangul, Halil Saglam, Yaman Saglam, et al.
Global Medical Genetics|August 25, 2021
Psychomotor Delay in a Child with <i>FGFR3</i> G380R Pathogenic Mutation Causing AchondroplasiaMahmut C Ergoren, Erdal Eren, Elena Manara, et al.
Hormone Molecular Biology and Clinical Investigation|September 27, 2018
Effect of experimentally induced hypothyroidism during gestation period on activity dependent neurotrophic factor (ADNF) in newborn rat brain tissueGökhan Cesur, Mehtap Kılıç Eren, Erdal Eren, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 30, 2025
Impact of the Transition Council in Type 1 Diabetes: Bridging the Gap to Adult CareErhan Hocaoglu, Hatice Nursoy, Filiz Mercan Saridas, et al.
Pageof 9