Mustafa Calik
Harran, Turkey
Last Updated: 09/26/2026
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Found 45 publications
Two rare autosomal recessive neurological disorders identified by combined genetic approaches in a single consanguineous family with multiple offspring.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: June 27, 2023
Association of NOD1 and NOD2 Polymorphisms With Susceptibility to Subacute Sclerosing Panencephalitis.
Journal: Journal of child neurology
Published: December 22, 2022
Correction: Risk Factors for Clinical Seizures in Neonates with Hypoxic-ischemic Encephalopathy Treated with Therapeutic Hypothermia.
Journal: Klinische Padiatrie
Published: July 06, 2022
Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study.
Journal: European journal of pediatrics
Published: March 09, 2021
Interleukin-33 and oxidative stress in epilepsy patients.
Journal: Epilepsy research
Published: December 29, 2020
Investigation of the plasma copeptin level in cases with childhood migraine.
Journal: Human & experimental toxicology
Published: December 09, 2020
Impaired Thiol/Disulfide Homeostasis in Children Diagnosed with Autism: A Case-Control Study.
Journal: Journal of molecular neuroscience : MN
Published: July 03, 2020
The Serum Prolidase Enzyme Activity as a Biomarker for Evaluation of the Subclinical Vascular Damage in Children with Epilepsy.
Journal: Annals of Indian Academy of Neurology
Published: December 05, 2019
Does B12 deficiency lead to change in brain metabolites in pediatric population? A MR spectroscopy study.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: March 28, 2019
Epidemiological and sociocultural assessment of childhood poisonings.
Journal: Turkish journal of emergency medicine
Published: March 08, 2019
Biallelic loss of EEF1D function links heat shock response pathway to autosomal recessive intellectual disability.
Journal: Journal of human genetics
Published: October 18, 2018
Last Updated: 09/26/2026