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Sensory processing patterns affect headache severity among adolescents with migraine

Journal of headache and pain, 2020-05, Vol.21 (1), p.48-7, Article 48

2020

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Handwriting in children with Attention Deficient Hyperactive Disorder: role of graphology

BMC pediatrics, 2019-12, Vol.19 (1), p.484-484, Article 484

2019

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Attention Deficit Hyperactivity Disorder in Neurofibromatosis Type 1: Evaluation with a Continuous Performance Test

Journal of Clinical Neurology, 2018, 14(2), , pp.153-157

2018

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Sensory Processing Difficulties Correlate With Disease Severity and Quality of Life Among Children With Migraine

Frontiers in neurology, 2019-05, Vol.10, p.448

2019

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Congenital myasthenic syndrome in Israel: Genetic and clinical characterization

Neuromuscular disorders : NMD, 2017-02, Vol.27 (2), p.136-140

2017

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Prospective, Cross-Sectional Study Finds No Common Viruses in Cerebrospinal Fluid of Children with Pseudotumor Cerebri

Brain sciences, 2023-02, Vol.13 (2), p.361

2023

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Children's Sleep Disturbance Scale in Differentiating Neurological Disorders

Pediatric neurology, 2013-12, Vol.49 (6), p.465-468

2013

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High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri Syndrome

Children (Basel), 2023-06, Vol.10 (7), p.1122

2023

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Thick Corpus Callosum in Children

Journal of Clinical Neurology, 2017, 13(2), , pp.170-174

2017

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Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblings

European journal of paediatric neurology, 2014-09, Vol.18 (5), p.567-571

2014

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Microcephaly Thin Corpus Callosum Intellectual Disability Syndrome Caused by Mutated TAF2

Pediatric neurology, 2013-12, Vol.49 (6), p.411-416.e1

2013

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Incidental Multifocal White Matter Lesions in Pediatric Magnetic Resonance Imaging

Pediatric neurology, 2012-07, Vol.47 (1), p.7-12

2012

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The Utility of Early Brain MRI for Patients with Neurofibromatosis Type 1 and Optic Pathway Glioma: A Long-Term Follow-Up in a Tertiary Referral Hospital

Neuropediatrics, 2022-10, Vol.53 (5), p.370-375

2022

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Microcephaly-Thin Corpus Callosum Syndrome Maps to 8q23.2-q24.12

Pediatric neurology, 2012-06, Vol.46 (6), p.363-368

2012

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Prognostic Parameters of Acute Transverse Myelitis in Children

Journal of child neurology, 2020-12, Vol.35 (14), p.999-1003

2020

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An update on the ketogenic diet, 2012

Rambam Maimonides medical journal, 2012-01, Vol.3 (1), p.e0005-e0005

2012

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Evolution of EEG Findings in Pontocerebellar Hypoplasia Type 2A: Normal EEG in the First Few Months followed by Abnormal Tracing over the Years

Neuropediatrics, 2020-12, Vol.51 (6), p.440-444

2020

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Methylphenidate Induction of Complex Visual Hallucinations

Journal of child neurology, 2009-08, Vol.24 (8), p.1005-1007

2009

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Development of Infants With Idiopathic External Hydrocephalus

Journal of child neurology, 2015-07, Vol.30 (8), p.1044-1047

2015

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Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN

Journal of medical genetics, 2011-06, Vol.48 (6), p.383-389

2011

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Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia

Journal of neurology, 2014-11, Vol.261 (11), p.2165-2169

2014

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Brain imaging findings and social/emotional problems in Israeli children with neurofibromatosis type 1

European journal of pediatrics, 2015-02, Vol.174 (2), p.199-203

2015

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Kyphoscoliosis peptidase (KY) mutation causes a novel congenital myopathy with core targetoid defects

Acta neuropathologica, 2016-09, Vol.132 (3), p.475-478

2016

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Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22

European journal of paediatric neurology, 2014-11, Vol.18 (6), p.801-805

2014

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Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene

Neurogenetics, 2014-05, Vol.15 (2), p.107-113

2014

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Sensory processing patterns affect headache severity among adolescents with migraine

Handwriting in children with Attention Deficient Hyperactive Disorder: role of graphology

Attention Deficit Hyperactivity Disorder in Neurofibromatosis Type 1: Evaluation with a Continuous Performance Test

Sensory Processing Difficulties Correlate With Disease Severity and Quality of Life Among Children With Migraine

Congenital myasthenic syndrome in Israel: Genetic and clinical characterization

Prospective, Cross-Sectional Study Finds No Common Viruses in Cerebrospinal Fluid of Children with Pseudotumor Cerebri

Children's Sleep Disturbance Scale in Differentiating Neurological Disorders

High CCL2 Levels Detected in CSF of Patients with Pediatric Pseudotumor Cerebri Syndrome

Thick Corpus Callosum in Children

Paternal germline mosaicism of a SCN2A mutation results in Ohtahara syndrome in half siblings

Microcephaly Thin Corpus Callosum Intellectual Disability Syndrome Caused by Mutated TAF2

Incidental Multifocal White Matter Lesions in Pediatric Magnetic Resonance Imaging

The Utility of Early Brain MRI for Patients with Neurofibromatosis Type 1 and Optic Pathway Glioma: A Long-Term Follow-Up in a Tertiary Referral Hospital

Microcephaly-Thin Corpus Callosum Syndrome Maps to 8q23.2-q24.12

Prognostic Parameters of Acute Transverse Myelitis in Children

An update on the ketogenic diet, 2012

Evolution of EEG Findings in Pontocerebellar Hypoplasia Type 2A: Normal EEG in the First Few Months followed by Abnormal Tracing over the Years

Methylphenidate Induction of Complex Visual Hallucinations

Development of Infants With Idiopathic External Hydrocephalus

Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN

Novel EXOSC3 mutation causes complicated hereditary spastic paraplegia

Brain imaging findings and social/emotional problems in Israeli children with neurofibromatosis type 1

Kyphoscoliosis peptidase (KY) mutation causes a novel congenital myopathy with core targetoid defects

Two siblings with early infantile myoclonic encephalopathy due to mutation in the gene encoding mitochondrial glutamate/H+ symporter SLC25A22

Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene

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