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Knowledge, attitudes, and practices among mothers of children with epilepsy: A study in a teaching hospital

Epilepsy & behavior, 2017-04, Vol.69, p.147-152

2017

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Analysis of the HEXA, HEXB, ARSA, and SMPD1 Genes in 68 Iranian Patients

Journal of molecular neuroscience, 2022-03, Vol.72 (3), p.555-564

2022

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Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutations

Hereditas, 2022-01, Vol.159 (1), p.8-8, Article 8

2022

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A Novel Homozygous ATP8A2 Variant in a Patient With Phenotypic Features of Dysequilibrium Syndrome

Acta medica Iranica, 2018-10, Vol.56 (10), p.677

2018

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Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group

BMC neurology, 2015-10, Vol.15 (1), p.205-205, Article 205

2015

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Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic Group

Journal of molecular neuroscience, 2016-07, Vol.59 (3), p.392-396

2016

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Neurobrucellosis: A Partially Treatable Cause of Vision Loss

Pediatric neurology, 2009-05, Vol.40 (5), p.401-403

2009

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Recurrent angioedema, Guillain-Barré, and myelitis in a girl with systemic lupus erythematosus and CD59 deficiency syndrome

Autoimmunity highlights, 2020-06, Vol.11 (1), p.9, Article 9

2020

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A comparison of buccal midazolam and intravenous diazepam for the acute treatment of seizures in children

Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2012-09, Vol.22 (3), p.303-308

2012

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Neurocognitive effects of phenobarbital discontinuation in epileptic children

Epilepsy & behavior, 2006-02, Vol.8 (1), p.145-148

2006

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Motor planning is not restricted to only one hemisphere: evidence from ERPs in individuals with hemiplegic cerebral palsy

Experimental brain research, 2022-09, Vol.240 (9), p.2311-2326

2022

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HEREDITARY SPASTIC PARAPLEGIA: FROM GENE TO CLINIC

Iranian journal of child neurology, 2010-03, Vol.3 (4), p.7-16

Tonekaboni, SH

2010

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Five patients with spinal muscular atrophy-progressive myoclonic epilepsy (SMA-PME): a novel pathogenic variant, treatment and review of the literature

Neuromuscular disorders : NMD, 2022-10, Vol.32 (10), p.806-810

2022

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Genetics of intellectual disability in consanguineous families

Molecular psychiatry, 2019-07, Vol.24 (7), p.1027-1039

2019

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Megaconial congenital muscular dystrophy due to CHKB gene variants, the first report of thirteen Iranian patients

Neuromuscular disorders : NMD, 2023-07, Vol.33 (7), p.589-595

2023

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The Effects of Sodium Valproate in Improving Developmental Delay in Seizure-Free Children with Abnormal Electroencephalography

Iranian journal of medical sciences, 2009-06, Vol.34 (2), p.110-115

2009

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Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection

Neurological sciences, 2023-12, Vol.44 (12), p.4491-4498

2023

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EFFICACY OF THE KETOGENIC DIET AS A THERAPY FOR INTRACTABLE EPILEPSY IN CHILDREN

Iranian journal of child neurology, 2010-09, Vol.4 (2), p.27-36

2010

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Neurodegeneration with brain iron accumulation: an overview

Iranian journal of child neurology, 2014-01, Vol.8 (4), p.1-8

2014

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Atypical presentations in an RTD patient and report of novel SLC52A3 and SLC52A2 mutations

Acta neurologica Belgica, 2024-07

2024

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Ryanodine receptor type 3 (RYR3) as a novel gene associated with a myopathy with nemaline bodies

European journal of neurology, 2018-06, Vol.25 (6), p.841-847

2018

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THE EFFECT OF THE KETOGENIC DIET ON THE GROWTH AND BIOCHEMICAL PARAMETERS OF THE CHILDREN WITH RESISTANT EPILEPSY

Iranian journal of child neurology, 2010-03, Vol.3 (4), p.41-44

2010

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A Novel Homozygous ATP8A2 Variant in a Patient With Phenotypic Features of Dysequilibrium Syndrome

Acta medica Iranica, 2019-01, Vol.56 (10)

2019

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Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome

European journal of medical genetics, 2018-10, Vol.61 (10), p.585-595

2018

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Epidemiology of Guillain-BarréSyndrome in Iranian Children Aged 0-15 Years (2008-2013)

Iranian journal of child neurology, 2021-10, Vol.15 (4), p.27

2021

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Knowledge, attitudes, and practices among mothers of children with epilepsy: A study in a teaching hospital

Analysis of the HEXA, HEXB, ARSA, and SMPD1 Genes in 68 Iranian Patients

Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutations

A Novel Homozygous ATP8A2 Variant in a Patient With Phenotypic Features of Dysequilibrium Syndrome

Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group

Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic Group

Neurobrucellosis: A Partially Treatable Cause of Vision Loss

Recurrent angioedema, Guillain-Barré, and myelitis in a girl with systemic lupus erythematosus and CD59 deficiency syndrome

A comparison of buccal midazolam and intravenous diazepam for the acute treatment of seizures in children

Neurocognitive effects of phenobarbital discontinuation in epileptic children

Motor planning is not restricted to only one hemisphere: evidence from ERPs in individuals with hemiplegic cerebral palsy

HEREDITARY SPASTIC PARAPLEGIA: FROM GENE TO CLINIC

Five patients with spinal muscular atrophy-progressive myoclonic epilepsy (SMA-PME): a novel pathogenic variant, treatment and review of the literature

Genetics of intellectual disability in consanguineous families

Megaconial congenital muscular dystrophy due to CHKB gene variants, the first report of thirteen Iranian patients

The Effects of Sodium Valproate in Improving Developmental Delay in Seizure-Free Children with Abnormal Electroencephalography

Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection

EFFICACY OF THE KETOGENIC DIET AS A THERAPY FOR INTRACTABLE EPILEPSY IN CHILDREN

Neurodegeneration with brain iron accumulation: an overview

Atypical presentations in an RTD patient and report of novel SLC52A3 and SLC52A2 mutations

Ryanodine receptor type 3 (RYR3) as a novel gene associated with a myopathy with nemaline bodies

THE EFFECT OF THE KETOGENIC DIET ON THE GROWTH AND BIOCHEMICAL PARAMETERS OF THE CHILDREN WITH RESISTANT EPILEPSY

A Novel Homozygous ATP8A2 Variant in a Patient With Phenotypic Features of Dysequilibrium Syndrome

Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome

Epidemiology of Guillain-BarréSyndrome in Iranian Children Aged 0-15 Years (2008-2013)

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