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Prognosis and demographic characteristics of SSPE patients in Istanbul, Turkey

Brain & development (Tokyo. 1979), 2015-06, Vol.37 (6), p.612-617

2015

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Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy

Nature genetics, 2015-01, Vol.47 (1), p.73-77

2015

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Acquired Chiari I Malformation Secondary to Spontaneous Intracranial Hypotension Syndrome and Persistent Hypoglycemia: A Case Report

Journal of clinical research in pediatric endocrinology, 2018-12, Vol.10 (4), p.391-394

2018

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The effects of nusinersen treatment on respiratory status of children with spinal muscular atrophy

Pediatrics international, 2022-01, Vol.64 (1), p.e15310-n/a

2022

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Exploring the Influence of Concurrent Nutritional Therapy on Children with Spinal Muscular Atrophy Receiving Nusinersen Treatment

Children (Basel), 2024-07, Vol.11 (8), p.886

2024

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MRS features during encephalopathic crisis period in 11 years old case with GA-1

Brain & development (Tokyo. 1979), 2015-05, Vol.37 (5), p.546-551

2015

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The Contribution of DTI in Determining the Relationship of Epilepsy and Brain Lesions in Children with Tuberous Sclerosis

Current medical imaging reviews, 2018-06, Vol.14 (3), p.401-406

2018

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Mixture models reveal multiple positional bias types in RNA-Seq data and lead to accurate transcript concentration estimates

PLoS computational biology, 2017-05, Vol.13 (5), p.e1005515

2017

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The impact of SARS-CoV2 on the anxiety levels of subjects and on the anxiety and depression levels of their parents

Multiple sclerosis and related disorders, 2021-01, Vol.47, p.102595-102595, Article 102595

2021

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Non epileptic paroxysmal events in childhood

Turk Pediatri Arsivi, 2017-06, Vol.52 (2), p.59-65

2017

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Evaluation of Clinical Findings and Molecular Genetic Results of the Patients with CACNA1A Variants: Single Center Experience (P13-9.007)

Neurology, 2023-04, Vol.100 (17_supplement_2)

2023

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Endocrinological Evaluations of a Neurofibromatosis Type 1 Cohort: Is it Necessary to Evaluate Autoimmune Thyroiditis in Neurofibromatosis Type 1?

Balkan medical journal, 2017-12, Vol.34 (6), p.522-526

2017

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The impact of epilepsy on preschool children and their families

Epilepsy & behavior, 2016-09, Vol.62, p.6-11

2016

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Rare vascular pathology sinus pericranii; becomes symptomatic with pseudotumor cerebri

Turkish journal of pediatrics, 2015-11, Vol.57 (6), p.618-620

2015

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P492 Electroclinical features and seizure outcome of peadiatric patients with immune mediated encephalopathy

Archives of disease in childhood, 2019-06, Vol.104 (Suppl 3), p.A349

2019

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Respiratory functions, respiratory muscle strength and fatigue in patients with pediatric-onset multiple sclerosis: a comparative cross-sectional study

Acta neurologica Belgica, 2024-08

2024

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Long-Term Disease Course of Pontocerebellar Hypoplasia Type 10

Pediatric neurology, 2024-09, Vol.158, p.1-10

2024

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Onychomadesis: A rare adverse effect in early-period valproic acid therapy

Turk Pediatri Arsivi, 2017-06, Vol.52 (2), p.98-100

2017

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Six-Minute Walk Performance and Related Factors in Pediatric-Onset Multiple Sclerosis

Journal of child neurology, 2022-04, Vol.37 (5), p.351-358

2022

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The effects of online exercise training on physical functions and quality of life in patients with pediatric-onset multiple sclerosis

Multiple sclerosis and related disorders, 2023-06, Vol.74, p.104710-104710, Article 104710

2023

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Children With Type 1 Interferonopathy: Commonalities and Diversities in a Large Patient Cohort

Journal of rheumatology, 2024-09, p.jrheum.2024-0294

2024

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Acute flaccid myelitis outbreak through 2016–2018: A multicenter experience from Turkey

European journal of paediatric neurology, 2021-01, Vol.30, p.113-120

2021

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Expanding Clinical Phenotype of TRAPPC12-Related Childhood Encephalopathy: Two Cases and Review of Literature

Neuropediatrics, 2020-12, Vol.51 (6), p.430-434

2020

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MRS features during encephalopathic crisis period in 11years old case with GA-1

Brain & development (Tokyo. 1979), 2015-05, Vol.37 (5), p.546-551

2015

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Report of a patient with Temple-Baraitser syndrome

American journal of medical genetics. Part A, 2014-03, Vol.164A (3), p.848-851

2014

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Prognosis and demographic characteristics of SSPE patients in Istanbul, Turkey

Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy

Acquired Chiari I Malformation Secondary to Spontaneous Intracranial Hypotension Syndrome and Persistent Hypoglycemia: A Case Report

The effects of nusinersen treatment on respiratory status of children with spinal muscular atrophy

Exploring the Influence of Concurrent Nutritional Therapy on Children with Spinal Muscular Atrophy Receiving Nusinersen Treatment

MRS features during encephalopathic crisis period in 11 years old case with GA-1

The Contribution of DTI in Determining the Relationship of Epilepsy and Brain Lesions in Children with Tuberous Sclerosis

Mixture models reveal multiple positional bias types in RNA-Seq data and lead to accurate transcript concentration estimates

The impact of SARS-CoV2 on the anxiety levels of subjects and on the anxiety and depression levels of their parents

Non epileptic paroxysmal events in childhood

Evaluation of Clinical Findings and Molecular Genetic Results of the Patients with CACNA1A Variants: Single Center Experience (P13-9.007)

Endocrinological Evaluations of a Neurofibromatosis Type 1 Cohort: Is it Necessary to Evaluate Autoimmune Thyroiditis in Neurofibromatosis Type 1?

The impact of epilepsy on preschool children and their families

Rare vascular pathology sinus pericranii; becomes symptomatic with pseudotumor cerebri

P492 Electroclinical features and seizure outcome of peadiatric patients with immune mediated encephalopathy

Respiratory functions, respiratory muscle strength and fatigue in patients with pediatric-onset multiple sclerosis: a comparative cross-sectional study

Long-Term Disease Course of Pontocerebellar Hypoplasia Type 10

Onychomadesis: A rare adverse effect in early-period valproic acid therapy

Six-Minute Walk Performance and Related Factors in Pediatric-Onset Multiple Sclerosis

The effects of online exercise training on physical functions and quality of life in patients with pediatric-onset multiple sclerosis

Children With Type 1 Interferonopathy: Commonalities and Diversities in a Large Patient Cohort

Acute flaccid myelitis outbreak through 2016–2018: A multicenter experience from Turkey

Expanding Clinical Phenotype of TRAPPC12-Related Childhood Encephalopathy: Two Cases and Review of Literature

MRS features during encephalopathic crisis period in 11years old case with GA-1

Report of a patient with Temple-Baraitser syndrome

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