Zuhal Yapıcı

Istanbul, Turkey

Last Updated: 09/26/2026

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Found 28 publications

Clinical Evaluation of Three KRS Families and Cellular Analysis of Distinct ATP13A2 Mutations Reveal Different Levels of Iron Accumulation.

Clinical Evaluation of Three KRS Families and Cellular Analysis of Distinct ATP13A2 Mutations Reveal Different Levels of Iron Accumulation.

Journal: Journal of neurochemistry
Published: October 21, 2025

Missense variants in PKAN: insights from a multi-patient genetic analysis.

Missense variants in PKAN: insights from a multi-patient genetic analysis.

Journal: Neurogenetics
Published: September 17, 2025

Quantitative Iron Measurements in the Basal Ganglia of NBIA Patients Using QSM: Insights From a Tertiary Center.

Quantitative Iron Measurements in the Basal Ganglia of NBIA Patients Using QSM: Insights From a Tertiary Center.

Journal: Annals of clinical and translational neurology
Published: February 27, 2025

Diffusion Tensor Imaging and Fiber Tractography Analysis in Patients with Pelizaeus-Merzbacher Disease.

Diffusion Tensor Imaging and Fiber Tractography Analysis in Patients with Pelizaeus-Merzbacher Disease.

Journal: Noro psikiyatri arsivi
Published: February 19, 2025

Effects of immune modulatory treatment on language and psychiatric profile in patients with electrical status epilepticus in sleep (ESES).

Effects of immune modulatory treatment on language and psychiatric profile in patients with electrical status epilepticus in sleep (ESES).

Journal: Epilepsy & behavior : E&B
Published: June 13, 2024

The Association Between Serum Levels of Glial Biomarkers, Clinical Severity and Electro-encephalography Features in Idiopathic West and Lennox-Gastaut Syndromes.

The Association Between Serum Levels of Glial Biomarkers, Clinical Severity and Electro-encephalography Features in Idiopathic West and Lennox-Gastaut Syndromes.

Journal: Noro psikiyatri arsivi
Published: November 24, 2023

Epilepsy in dystrophinopathies: A retrospective cohort and review of the literature.

Epilepsy in dystrophinopathies: A retrospective cohort and review of the literature.

Journal: Epilepsy & behavior : E&B
Published: October 14, 2023

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes.

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

Exome data of developmental and epileptic encephalopathy patients reveals de novo and inherited pathologic variants in epilepsy-associated genes.

Exome data of developmental and epileptic encephalopathy patients reveals de novo and inherited pathologic variants in epilepsy-associated genes.

Journal: Seizure
Published: February 24, 2023

MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia.

MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia.

Journal: Molecular genetics and genomics : MGG
Published: January 20, 2022

Headache in idiopathic/genetic epilepsy: Cluster analysis in a large cohort.

Headache in idiopathic/genetic epilepsy: Cluster analysis in a large cohort.

Journal: Epilepsia
Published: October 17, 2021

Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort.

Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort.

Journal: Neurology. Genetics
Published: April 09, 2021
Showing 1-12 of 28

Last Updated: 09/26/2026