Cengiz Dilber
Kahramanmaras, Turkey
Last Updated: 09/26/2026
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Found 23 publications
Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study.
Journal: Cerebellum (London, England)
Published: March 27, 2024
The effect of proprioceptive neuromuscular facilitation on functional skills, muscle strength, and trunk control in children with cerebral palsy: A randomized controlled trial.
Journal: Early human development
Published: March 22, 2024
Distinctive sleep complaints and polysomnographic findings in antibody subgroups of autoimmune limbic encephalitis.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: March 14, 2024
Shared Biological Pathways and Processes in Patients with Intellectual Disability: A Multicenter Study.
Journal: Neuropediatrics
Published: February 14, 2023
Novel homozygous AP3B2 mutations in four individuals with developmental and epileptic encephalopathy: A rare clinical entity.
Journal: Clinical neurology and neurosurgery
Published: August 18, 2022
Therapeutic Plasma Exchange in Pediatric Patients: Results from a Single Center.
Journal: Journal of pediatric intensive care
Published: September 17, 2021
Predictive value of cardiac markers in the prognosis of COVID-19 in children.
Journal: The American journal of emergency medicine
Published: April 23, 2021
Evaluation of oxidative stress biomarkers in acute mercury intoxication.
Journal: Folia medica
Published: July 02, 2020
Vanishing white matter disease with different faces.
Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: June 15, 2019
Muscular Dystrophy: A Retrospective Evaluation of 15 Cases.
Journal: Sisli Etfal Hastanesi tip bulteni
Published: June 17, 2017
Acute Mercury Poisoning in a Group of School Children.
Journal: Pediatric emergency care
Published: December 16, 2016
Exome sequencing identifies a novel homozygous CLN8 mutation in a Turkish family with Northern epilepsy.
Journal: Acta neurologica Belgica
Published: September 14, 2016
Last Updated: 09/26/2026