Deniz Yuksel

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

A novel NT5C2 Variant in a Family with Spastic Paraplegia and Intellectual Disability.

Journal: Klinische Padiatrie

Published: December 09, 2025

Muscle Biopsy as a Decisive Tool in a Pediatric Case with Overlapping Genetic Findings for McArdle Disease and Dystrophinopathy.

Journal: Klinische Padiatrie

Published: August 11, 2025

The genetic landscape of childhood-onset dystonia in a nationwide Turkish cohort: Clinical spectrum, molecular diagnostics, and therapeutic implications.

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

Published: June 30, 2025

A Founder Allele in SGCG Combining Missense Variant and Multi-Exon Duplication in Turkish Patients With Sarcoglycanopathy.

Journal: Clinical genetics

Published: June 03, 2025

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

Journal: Journal of child neurology

Published: May 09, 2025

MRI findings in pediatric idiopathic intracranial hypertension: evaluating the oculomotor nerve sheath as a potential new diagnostic marker.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: March 27, 2025

A Novel Neuromodulation Method for Childhood Migraine: Comparing Noninvasive Pulsed Radiofrequency Therapy With Calcium Channel Blockers, a Randomized Controlled Trial.

Journal: Pediatric neurology

Published: March 06, 2025

Optical coherence tomography and angiography reveal early retinal alterations in pediatric-onset multiple sclerosis.

Journal: European journal of pediatrics

Published: February 10, 2025

Approach to childhood tremors: Insights from a pediatric neurologist.

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

Published: December 20, 2024

Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohort.

Journal: Frontiers in neurology

Published: December 07, 2024

Biallelic truncating variants in PACSIN3 cause childhood-onset myopathy with hyperCKaemia.

Journal: Brain : a journal of neurology

Published: March 15, 2024

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.

A novel NT5C2 Variant in a Family with Spastic Paraplegia and Intellectual Disability.

A novel NT5C2 Variant in a Family with Spastic Paraplegia and Intellectual Disability.

Muscle Biopsy as a Decisive Tool in a Pediatric Case with Overlapping Genetic Findings for McArdle Disease and Dystrophinopathy.

Muscle Biopsy as a Decisive Tool in a Pediatric Case with Overlapping Genetic Findings for McArdle Disease and Dystrophinopathy.

The genetic landscape of childhood-onset dystonia in a nationwide Turkish cohort: Clinical spectrum, molecular diagnostics, and therapeutic implications.

The genetic landscape of childhood-onset dystonia in a nationwide Turkish cohort: Clinical spectrum, molecular diagnostics, and therapeutic implications.

A Founder Allele in SGCG Combining Missense Variant and Multi-Exon Duplication in Turkish Patients With Sarcoglycanopathy.

A Founder Allele in SGCG Combining Missense Variant and Multi-Exon Duplication in Turkish Patients With Sarcoglycanopathy.

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.

MRI findings in pediatric idiopathic intracranial hypertension: evaluating the oculomotor nerve sheath as a potential new diagnostic marker.

MRI findings in pediatric idiopathic intracranial hypertension: evaluating the oculomotor nerve sheath as a potential new diagnostic marker.

A Novel Neuromodulation Method for Childhood Migraine: Comparing Noninvasive Pulsed Radiofrequency Therapy With Calcium Channel Blockers, a Randomized Controlled Trial.

A Novel Neuromodulation Method for Childhood Migraine: Comparing Noninvasive Pulsed Radiofrequency Therapy With Calcium Channel Blockers, a Randomized Controlled Trial.

Optical coherence tomography and angiography reveal early retinal alterations in pediatric-onset multiple sclerosis.

Optical coherence tomography and angiography reveal early retinal alterations in pediatric-onset multiple sclerosis.

Approach to childhood tremors: Insights from a pediatric neurologist.

Approach to childhood tremors: Insights from a pediatric neurologist.

Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohort.

Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohort.

Biallelic truncating variants in PACSIN3 cause childhood-onset myopathy with hyperCKaemia.

Biallelic truncating variants in PACSIN3 cause childhood-onset myopathy with hyperCKaemia.

Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohort.

Nusinersen for children with type I spinal muscular atrophy: 4 years' clinical experience in Turkish cohort.