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Eda Utine

Showing results (81-90 of 155) with videos related to

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American Journal of Perinatology|November 8, 2017
Prenatal and Postnatal Follow-up in Trisomies 13 and 18: A 20-Year Experience in a Tertiary CenterÖzlem Akgün Doğan, Gizem Ürel Demir, Umut Arslan, et al.
Molecular Syndromology|November 23, 2020
Hyperinsulinemic Hypoglycemia in a Patient with Costello Syndrome: An Etiology to Consider in HypoglycemiaDogus Vuralli, Can Kosukcu, Ekim Taskiran, et al.
Fetal and Pediatric Pathology|December 9, 2017
Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex DevelopmentGizem Ürel Demir, Özlem Akgün Doğan, Pelin Özlem Şimşek Kiper, et al.
European Journal of Pediatrics|May 20, 2025
Recognizing multiple epiphyseal dysplasia in children presenting with joint pain: a commonly overlooked skeletal dysplasiaTuğba Daşar, Gözde İmren, Adalet Elçin Yıldız, et al.
Movement Disorders Clinical Practice|August 28, 2023
Cockayne syndrome type 3 with dystonia-ataxia and clicking blinksÖzge Berna Gültekin-Zaim, Gül Yalçın-Çakmaklı, Ayşe İlksen Çolpak, et al.
The Turkish Journal of Pediatrics|August 14, 2018
Clinical and molecular evaluation of 16 patients with Rett syndromePınar Zengin-Akkuş, Ekim Z Taşkıran, Serkan Kabaçam, et al.
Journal of Child Neurology|April 25, 2013
A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophyG Eda Utine, Göknur Haliloğlu, Bilge Salanci, et al.
Molecular Syndromology|January 29, 2021
Molecular Etiology of Isolated Congenital Cataract Using Next-Generation Sequencing: Single Center Exome Sequencing Data from TurkeyHande Taylan Sekeroglu, Beren Karaosmanoglu, Ekim Z Taskiran, et al.
Journal of Pediatric and Adolescent Gynecology|March 8, 2023
Assessing the Menstrual Cycle and Related Problems in Adolescents with a Genetic Syndrome Associated with Intellectual DisabilityHande Üçler Çınar, Melis Pehlivantürk Kızılkan, Akçahan Akalın, et al.
Blood Pressure Monitoring|January 19, 2022
Apparent mineralocorticoid excess: A diagnosis beyond classical causes of severe hypertension in a childBora Gulhan, Yağmur Ünsal, Demet Baltu, et al.
Pageof 16

Showing results (81-90 of 155) with videos related to

Sort By:
Pageof 16
American Journal of Perinatology|November 8, 2017
Prenatal and Postnatal Follow-up in Trisomies 13 and 18: A 20-Year Experience in a Tertiary CenterÖzlem Akgün Doğan, Gizem Ürel Demir, Umut Arslan, et al.
Molecular Syndromology|November 23, 2020
Hyperinsulinemic Hypoglycemia in a Patient with Costello Syndrome: An Etiology to Consider in HypoglycemiaDogus Vuralli, Can Kosukcu, Ekim Taskiran, et al.
Fetal and Pediatric Pathology|December 9, 2017
Coexistence of Trisomy 13 and SRY (-) XX Ovotesticular Disorder of Sex DevelopmentGizem Ürel Demir, Özlem Akgün Doğan, Pelin Özlem Şimşek Kiper, et al.
European Journal of Pediatrics|May 20, 2025
Recognizing multiple epiphyseal dysplasia in children presenting with joint pain: a commonly overlooked skeletal dysplasiaTuğba Daşar, Gözde İmren, Adalet Elçin Yıldız, et al.
Movement Disorders Clinical Practice|August 28, 2023
Cockayne syndrome type 3 with dystonia-ataxia and clicking blinksÖzge Berna Gültekin-Zaim, Gül Yalçın-Çakmaklı, Ayşe İlksen Çolpak, et al.
The Turkish Journal of Pediatrics|August 14, 2018
Clinical and molecular evaluation of 16 patients with Rett syndromePınar Zengin-Akkuş, Ekim Z Taşkıran, Serkan Kabaçam, et al.
Journal of Child Neurology|April 25, 2013
A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophyG Eda Utine, Göknur Haliloğlu, Bilge Salanci, et al.
Molecular Syndromology|January 29, 2021
Molecular Etiology of Isolated Congenital Cataract Using Next-Generation Sequencing: Single Center Exome Sequencing Data from TurkeyHande Taylan Sekeroglu, Beren Karaosmanoglu, Ekim Z Taskiran, et al.
Journal of Pediatric and Adolescent Gynecology|March 8, 2023
Assessing the Menstrual Cycle and Related Problems in Adolescents with a Genetic Syndrome Associated with Intellectual DisabilityHande Üçler Çınar, Melis Pehlivantürk Kızılkan, Akçahan Akalın, et al.
Blood Pressure Monitoring|January 19, 2022
Apparent mineralocorticoid excess: A diagnosis beyond classical causes of severe hypertension in a childBora Gulhan, Yağmur Ünsal, Demet Baltu, et al.
Pageof 16