Esra Sarigecili

Adana, Turkey

Last Updated: 09/26/2026

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Found 21 publications

Effects of newborn screening and nusinersen on survival and functional outcomes in spinal muscular atrophy with two SMN2 copies: A nationwide multicentre real-world study from Turkey.

Effects of newborn screening and nusinersen on survival and functional outcomes in spinal muscular atrophy with two SMN2 copies: A nationwide multicentre real-world study from Turkey.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: March 15, 2026

From Misdiagnosis to Treatment: Genetic Landscape and Genotype-Phenotype Correlations of Hyperekplexia.

From Misdiagnosis to Treatment: Genetic Landscape and Genotype-Phenotype Correlations of Hyperekplexia.

Journal: Pediatric neurology

Published: January 22, 2026

Clinicoradiologic Features and Genetic Findings of Infantile Neuroaxonal Dystrophy.

Clinicoradiologic Features and Genetic Findings of Infantile Neuroaxonal Dystrophy.

Journal: Journal of child neurology

Published: August 04, 2025

A Multisystem Perspective of Pediatric Cell Trafficking Disorders: Within the Cells, Beneath the Signs.

A Multisystem Perspective of Pediatric Cell Trafficking Disorders: Within the Cells, Beneath the Signs.

Journal: JIMD reports

Published: July 27, 2025

Acute Disseminated Encephalomyelitis in Children and Adolescents: A Multicenter Retrospective Study of Relapse and Outcome.

Acute Disseminated Encephalomyelitis in Children and Adolescents: A Multicenter Retrospective Study of Relapse and Outcome.

Journal: Journal of child neurology

Published: May 09, 2025

Phenotypic variability in cases with CACNA1A mutation.

Phenotypic variability in cases with CACNA1A mutation.

Journal: European journal of pediatrics

Published: November 21, 2024

First-Drug Efficacy and Drug-Resistant Epilepsy Rates in Children With New-Onset Epilepsies: A Multicenter Large Cohort Study.

First-Drug Efficacy and Drug-Resistant Epilepsy Rates in Children With New-Onset Epilepsies: A Multicenter Large Cohort Study.

Journal: Journal of child neurology

Published: September 30, 2024

Optic neuritis in Turkish children and adolescents: A multicenter retrospective study.

Optic neuritis in Turkish children and adolescents: A multicenter retrospective study.

Journal: Multiple sclerosis and related disorders

Published: September 14, 2023

Short-Term and Long-Term Effects of Levetiracetam Monotherapy On Hematological Parameters in Children with Idiopathic Epilepsy.

Short-Term and Long-Term Effects of Levetiracetam Monotherapy On Hematological Parameters in Children with Idiopathic Epilepsy.

Journal: Sisli Etfal Hastanesi tip bulteni

Published: June 16, 2022

A Rare Cause of Paroxysmal Movement Disorder Associated with TBC1D24 Gene Mutation in Two Siblings.

A Rare Cause of Paroxysmal Movement Disorder Associated with TBC1D24 Gene Mutation in Two Siblings.

Journal: Annals of Indian Academy of Neurology

Published: May 25, 2022

Acute necrotizing encephalopathy associated with RANBP2 mutation: value of MRI findings for diagnosis and intervention.

Acute necrotizing encephalopathy associated with RANBP2 mutation: value of MRI findings for diagnosis and intervention.

Journal: Acta neurologica Belgica

Published: March 31, 2022

A rare cause of microcephaly, thin corpus callosum and refractory epilepsy due to a novel SLC1A4 gene mutation.

A rare cause of microcephaly, thin corpus callosum and refractory epilepsy due to a novel SLC1A4 gene mutation.

Journal: Clinical neurology and neurosurgery

Published: February 13, 2022

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Last Updated: 09/26/2026