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Pediatrics International : Official Journal of the Japan Pediatric Society
|
August 21, 2010
Somatostatin for the treatment of chylothorax in a premature baby with Down syndrome
Meltem Ugras, Cengiz Yakinci, Bilge Ozgor
Journal of Pediatric Neurosciences
|
October 12, 2020
A Novel <i>SCN1A</i> Mutation: A Case Report
Mahmut Aslan, Bilge Ozgor, Serkan Kirik, et al.
Brain & Development
|
December 20, 2024
Novel biallelic nonsense mutation in IGHMBP2 gene linked to neuropathy (CMT2S): A comprehensive clinical, genetic and bioinformatic analysis of a Turkish patient with literature review
Cüneyd Yavas, Mustafa Dogan, Bilge Ozgor, et al.
IBRO Neuroscience Reports
|
March 30, 2026
Differential quadruple pattern: A new EEG signal classification framework
Bilge Ozgor, Omer Faruk Goktas, Mehmet Baygin, et al.
Molecular Syndromology
|
April 3, 2025
Exploring the Genetic Etiology of Pediatric Epilepsy: Insights from Targeted Next-Generation Sequence Analysis
Ozden Ozturk, Murat Ozturk, Kubra Ates, et al.
Molecular Syndromology
|
January 7, 2026
Molecular and Clinical Profiles of Patients with RASopathies: Targeted Next-Generation Sequencing Panel Results and Identification of 14 Novel Disease-Causing Variants
Kubra Ates, Murat Ozturk, Zeynep Esener, et al.
Neuropediatrics
|
February 14, 2023
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study
Çağatay Günay, Duygu Aykol, Özlem Özsoy, et al.
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Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
Pediatrics International : Official Journal of the Japan Pediatric Society
|
August 21, 2010
Somatostatin for the treatment of chylothorax in a premature baby with Down syndrome
Meltem Ugras, Cengiz Yakinci, Bilge Ozgor
Journal of Pediatric Neurosciences
|
October 12, 2020
A Novel <i>SCN1A</i> Mutation: A Case Report
Mahmut Aslan, Bilge Ozgor, Serkan Kirik, et al.
Brain & Development
|
December 20, 2024
Novel biallelic nonsense mutation in IGHMBP2 gene linked to neuropathy (CMT2S): A comprehensive clinical, genetic and bioinformatic analysis of a Turkish patient with literature review
Cüneyd Yavas, Mustafa Dogan, Bilge Ozgor, et al.
IBRO Neuroscience Reports
|
March 30, 2026
Differential quadruple pattern: A new EEG signal classification framework
Bilge Ozgor, Omer Faruk Goktas, Mehmet Baygin, et al.
Molecular Syndromology
|
April 3, 2025
Exploring the Genetic Etiology of Pediatric Epilepsy: Insights from Targeted Next-Generation Sequence Analysis
Ozden Ozturk, Murat Ozturk, Kubra Ates, et al.
Molecular Syndromology
|
January 7, 2026
Molecular and Clinical Profiles of Patients with RASopathies: Targeted Next-Generation Sequencing Panel Results and Identification of 14 Novel Disease-Causing Variants
Kubra Ates, Murat Ozturk, Zeynep Esener, et al.
Neuropediatrics
|
February 14, 2023
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study
Çağatay Günay, Duygu Aykol, Özlem Özsoy, et al.
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of 1