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Archivos Argentinos De Pediatria|May 11, 2016
Nonketotic hyperglycinemia: novel mutation in the aminomethyl transferase gene. Case reportPinar Gencpinar, Dilek Çavuşoğlu, Ömer Özbeyler, et al.
The Neuroradiology Journal|May 8, 2026
Neuroimaging spectrum of immune-mediated central nervous system disorders in children following SARS-CoV-2 infection: A case seriesOlgay Bildik, Gunce Basarir, Nargiz Aliyeva, et al.
Journal of Pediatric Genetics|May 1, 2018
A De Novo Xp11.23 Duplication in a Girl with a Severe Phenotype: Expanding the Clinical SpectrumPinar Arican, Dilek Cavusoglu, Pinar Gencpinar, et al.
Journal of Child Neurology|January 8, 2016
Evaluation of Executive Functions in Patients With Childhood Absence EpilepsyPinar Gencpinar, Zuhal Kalay, Sevil Turgut, et al.
Brain & Development|June 9, 2022
A female case of 5,10-methenyltetrahydrofolate synthetase deficiency with novel neuro-imaging abnormalitiesDilek Cavusoglu, Melis Kose, Esra Er, et al.
Journal of Neurovirology|April 23, 2016
Interleukin-12 (-1188) A/C and interferon-γ (+874) A/T gene polymorphisms in subacute sclerosing panencephalitis patientsNihal Olgac Dundar, Pinar Gencpinar, Nilgun Sallakci, et al.
Pediatric Neurology|June 16, 2019
The Clinical and Molecular Characteristics of Molybdenum Cofactor Deficiency Due to MOCS2 MutationsPinar Arican, Pinar Gencpinar, Ozgur Kirbiyik, et al.
Clinical Pediatrics|January 24, 2023
Evaluation of Nonconvulsive Status Epilepticus and Nonconvulsive Seizures in a Pediatric Intensive Care UnitDilek Cavusoglu, Nihal Olgac Dundar, Fulya Kamit, et al.
Developmental Psychobiology|May 5, 2026
Correlation of Neonatal Imitation and General Movements Assessment in Late Preterm InfantsMürüvvet Elif Şimşir, Defne Engur, Canberk Yılmaz, et al.
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