Hulya Maras-Genc

Istanbul, Turkey

Last Updated: 09/26/2026

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Found 20 publications

Primary headaches in juvenile-onset systemic lupus erythematosus: A preliminary case control study using ICHD-3 criteria.

Primary headaches in juvenile-onset systemic lupus erythematosus: A preliminary case control study using ICHD-3 criteria.

Journal: Lupus
Published: April 20, 2026

Unmasking genetic etiologies in neurodevelopmental disorders characterized by Cerebral Palsy: insights from integrative genomic approaches.

Unmasking genetic etiologies in neurodevelopmental disorders characterized by Cerebral Palsy: insights from integrative genomic approaches.

Journal: Frontiers in neurology
Published: November 08, 2025

Evaluation of perinatal arterial ischemic stroke patients: Underlying etiologic factors and long-term prognosis.

Evaluation of perinatal arterial ischemic stroke patients: Underlying etiologic factors and long-term prognosis.

Journal: Brain & development
Published: August 13, 2025

Case Report: Pediatric age onset CNTN1 antibody-associated neuropathy with nephropathy and literature review.

Case Report: Pediatric age onset CNTN1 antibody-associated neuropathy with nephropathy and literature review.

Journal: Frontiers in immunology
Published: December 21, 2024

Machine learning models for predicting treatment response in infantile epilepsies.

Machine learning models for predicting treatment response in infantile epilepsies.

Journal: Epilepsy & behavior : E&B
Published: May 20, 2024

Voltage-gated sodium channel epilepsies in a tertiary care center: Phenotypic spectrum with correlation to predicted functional effects.

Voltage-gated sodium channel epilepsies in a tertiary care center: Phenotypic spectrum with correlation to predicted functional effects.

Journal: Epilepsy & behavior : E&B
Published: February 29, 2024

A rare cause of arterial hypertension in a child with developmental delay: Answers.

A rare cause of arterial hypertension in a child with developmental delay: Answers.

Journal: Pediatric nephrology (Berlin, Germany)
Published: September 13, 2021

A rare cause of arterial hypertension in a child with developmental delay: Questions.

A rare cause of arterial hypertension in a child with developmental delay: Questions.

Journal: Pediatric nephrology (Berlin, Germany)
Published: September 13, 2021

Proteomic Analysis of m.8296A>G Variation in the Mitochondrial tRNA Lys Gene.

Proteomic Analysis of m.8296A>G Variation in the Mitochondrial tRNA Lys Gene.

Journal: Molecular syndromology
Published: April 17, 2021

BEND4 as a Candidate Gene for an Infection-Induced Acute Encephalopathy Characterized by a Cyst and Calcification of the Pons and Cerebellar Atrophy.

BEND4 as a Candidate Gene for an Infection-Induced Acute Encephalopathy Characterized by a Cyst and Calcification of the Pons and Cerebellar Atrophy.

Journal: Molecular syndromology
Published: March 03, 2021

Cytotoxic lesions of the corpus callosum in children: Etiology, clinical and radiological features, and prognosis.

Cytotoxic lesions of the corpus callosum in children: Etiology, clinical and radiological features, and prognosis.

Journal: Brain & development
Published: November 10, 2020

Vanishing white matter disease with different faces.

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
Showing 1-12 of 20

Last Updated: 09/26/2026