Mutluay M. Arslan
Ankara, Turkey
Last Updated: 09/26/2026
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Found 46 publications
Diagnostic value of machine-learning using conventional magnetic resonance imaging markers for pediatric idiopathic intracranial hypertension: a retrospective study.
Journal: Pediatric radiology
Published: February 27, 2026
Neurological complications of rotavirus infection in pediatric patients: a retrospective cohort study.
Journal: Acta neurologica Belgica
Published: February 08, 2026
Evaluation of resilience in pediatric well-controlled epilepsy patients.
Journal: Clinical neurology and neurosurgery
Published: November 23, 2024
Evaluation of the factors affecting mortality after cardiac arrest - do lactate and procalcitonin concentrations have any implications?
Journal: European review for medical and pharmacological sciences
Published: May 20, 2024
Can serum orexin levels be used as a marker in childhood epilepsy?
Journal: Heliyon
Published: February 06, 2024
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.
Journal: medRxiv : the preprint server for health sciences
Published: March 03, 2023
POU3F3-related disorder: Defining the phenotype and expanding the molecular spectrum.
Journal: Clinical genetics
Published: January 23, 2023
Three Afghani siblings with a novel homozygous variant and further delineation of the clinical features of METTL5 related intellectual disability syndrome.
Journal: The Turkish journal of pediatrics
Published: October 28, 2022
Clinical Heterogeneity in MT-ATP6 Pathogenic Variants: Same Genotype-Different Onset.
Journal: Cells
Published: November 09, 2021
The relationship of motor development with sensory processing among infants born very preterm: a prospective case-control study.
Journal: The Turkish journal of pediatrics
Published: November 05, 2021
Transient Neonatal Diabetes Mellitus and Seizure with an Unknown Etiology.
Journal: Journal of pediatric genetics
Published: December 21, 2020
Coexistence of severe developmental delay, epilepsy, and hemangioma in Snijders Blok-Fisher syndrome suggests the presence of a POU3F3-related SNIBFIS endophenotype: A case report.
Journal: American journal of medical genetics. Part A
Published: November 11, 2020
Last Updated: 09/26/2026