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A patient with neurofibromatosis type 1 and myotonic dystrophy type 1

Neurology Asia, 2022-06, Vol.27 (2), p.503-506

2022

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Lesional resective epilepsy surgery in childhood: Comparison of two decades and long-term seizure outcome from a single center

Epilepsy research, 2022-03, Vol.181, p.106882-106882, Article 106882

2022

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Neurologic manifestations in children with COVID-19 from a tertiary center in Turkey and literature review

European journal of paediatric neurology, 2022-03, Vol.37, p.139-154

2022

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International consensus classification of hippocampal sclerosis and etiologic diversity in children with temporal lobectomy

Epilepsy & behavior, 2020-11, Vol.112, p.107380-107380, Article 107380

2020

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Horizontal gaze palsy with progressive scoliosis: Further expanding the ROBO3 spectrum

Annals of clinical and translational neurology, 2024-08, Vol.11 (8), p.2088-2099

2024

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Neurologic manifestations in children with COVID-19

European journal of paediatric neurology, 2022-07, Vol.39, p.118-119

2022

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Etiological and Clinical Profile of Acute Nonbacterial Encephalitis in Children: A Single-Center Prospective Study

Neuropediatrics, 2021-12, Vol.52 (6), p.448-454

2021

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Basal Serum Thyroxine Level should Guide Initial Thyroxine Replacement Dose in Neonates with Congenital Hypothyroidism

Journal of clinical research in pediatric endocrinology, 2021-09, Vol.13 (3), p.269-275

2021

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Biallelic mutations in ELFN1 gene associated with developmental and epileptic encephalopathy and joint laxity

European journal of medical genetics, 2021-11, Vol.64 (11), p.104340-104340, Article 104340

2021

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Role of serostatus in pediatric neuromyelitis optica spectrum disorders: A nationwide multicentric study

Multiple sclerosis and related disorders, 2023-09, Vol.77, p.104847-104847, Article 104847

2023

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Electroencephalographic abnormalities in children with type 1 diabetes mellitus: a prospective study

Turkish journal of medical sciences, 2023-01, Vol.53 (6), p.1794-1798

2023

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Dihydropyrimidinase deficiency with atrioventricular septal defect: a case report

Journal of Pediatric Endocrinology and Metabolism, 2024-08, Vol.37 (8), p.741-744

2024

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Ifosfamide-induced Encephalopathy With Rapid Response to Thiamine: A Pediatric Case

Journal of pediatric hematology/oncology, 2022-10, Vol.44 (7), p.402-404

2022

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Optic neuropathies in childhood: a review of etiology and treatment

Turkish journal of pediatrics, 2019, Vol.61 (4), p.471-476

2019

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Unraveling neuronal ceroid lipofuscinosis type 2 (CLN2) disease: A tertiary center experience for determinants of diagnostic delay

European journal of paediatric neurology, 2021-07, Vol.33, p.94-98

2021

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Behavioral problems of preschool children with new-onset epilepsy and one-year follow-up — A prospective study

Epilepsy & behavior, 2019-03, Vol.92, p.171-175

2019

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Non-epileptic paroxysmal events at pediatric video-electroencephalography monitoring unit over a 15-year period

Seizure (London, England), 2023-05, Vol.108, p.89-95

2023

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Cardiac autonomic function evaluation in pediatric and adult patients with congenital myasthenic syndromes

Neuromuscular disorders : NMD, 2019-04, Vol.29 (4), p.290-295

2019

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Is There a Tendency for Autoimmunity in Neurofibromatosis Type 1? —Case Reports

Indian journal of pediatrics, 2022-05, Vol.89 (5), p.510-512

2022

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Relationship among four functional classification systems and parent interpredicted intelligence level in children with different clinical types of cerebral palsy

Developmental neurorehabilitation, 2022-08, Vol.25 (6), p.410-416

2022

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Myasthenia gravis in a patient with neurofibromatosis type 1

European journal of paediatric neurology, 2017-06, Vol.21, p.e112-e112

2017

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Concurrence of juvenile idiopathic arthritis and primary demyelinating disease in a young child

Multiple sclerosis and related disorders, 2019-01, Vol.27, p.20-22

2019

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Susceptibility-Weighted Magnetic Resonance Imaging Findings of Two Pediatric Migraine Patients with Aura

Neuropediatrics, 2016-01, Vol.47 (1), p.46-50

2016

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Autonomic functions in patients with congenital myasthenic syndrome due to mutations in the acetylcholine receptor epsilon subunit

European journal of paediatric neurology, 2017-06, Vol.21, p.e56-e56

2017

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A patient with neurofibromatosis type 1 and myotonic dystrophy type 1

Lesional resective epilepsy surgery in childhood: Comparison of two decades and long-term seizure outcome from a single center

Neurologic manifestations in children with COVID-19 from a tertiary center in Turkey and literature review

International consensus classification of hippocampal sclerosis and etiologic diversity in children with temporal lobectomy

Horizontal gaze palsy with progressive scoliosis: Further expanding the ROBO3 spectrum

Neurologic manifestations in children with COVID-19

Etiological and Clinical Profile of Acute Nonbacterial Encephalitis in Children: A Single-Center Prospective Study

Basal Serum Thyroxine Level should Guide Initial Thyroxine Replacement Dose in Neonates with Congenital Hypothyroidism

Biallelic mutations in ELFN1 gene associated with developmental and epileptic encephalopathy and joint laxity

Role of serostatus in pediatric neuromyelitis optica spectrum disorders: A nationwide multicentric study

Electroencephalographic abnormalities in children with type 1 diabetes mellitus: a prospective study

Dihydropyrimidinase deficiency with atrioventricular septal defect: a case report

Ifosfamide-induced Encephalopathy With Rapid Response to Thiamine: A Pediatric Case

Optic neuropathies in childhood: a review of etiology and treatment

Evaluation of immunization status in patients with cerebral palsy: a multicenter CP-VACC study

Unraveling neuronal ceroid lipofuscinosis type 2 (CLN2) disease: A tertiary center experience for determinants of diagnostic delay

Behavioral problems of preschool children with new-onset epilepsy and one-year follow-up — A prospective study

Non-epileptic paroxysmal events at pediatric video-electroencephalography monitoring unit over a 15-year period

Cardiac autonomic function evaluation in pediatric and adult patients with congenital myasthenic syndromes

Is There a Tendency for Autoimmunity in Neurofibromatosis Type 1? —Case Reports

Relationship among four functional classification systems and parent interpredicted intelligence level in children with different clinical types of cerebral palsy

Myasthenia gravis in a patient with neurofibromatosis type 1

Concurrence of juvenile idiopathic arthritis and primary demyelinating disease in a young child

Susceptibility-Weighted Magnetic Resonance Imaging Findings of Two Pediatric Migraine Patients with Aura

Autonomic functions in patients with congenital myasthenic syndrome due to mutations in the acetylcholine receptor epsilon subunit

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