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Risk factors of pediatric arterial ischemic stroke; A regional survey

International journal of preventive medicine, 2018-01, Vol.9 (1), p.69-69

2018

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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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Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism

BMC medical genomics, 2024-08, Vol.17 (1), p.196-15, Article 196

2024

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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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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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Mitochondrial Copy Number and D-Loop Variants in Pompe Patients

Cell journal (Yakhteh), 2016, Vol.18 (3), p.405-415

2016

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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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Neurobrucellosis: A Partially Treatable Cause of Vision Loss

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

2009

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Investigation of microdeletions in syndromic intellectual disability by MLPA in Iranian population

Archives of Iranian medicine, 2014-07, Vol.17 (7), p.471

2014

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Recurrence of Developmental and Epileptic Encephalopathy 9 (DEE9) in Two Siblings Due to Parental Germline Mosaicism of PCDH19 Mutation and Review of the Literature

Basic and clinical neuroscience, 2024-07, Vol.15 (4)

2024

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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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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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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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Specific Anti Mumps Antibodies (IgG IgM) in Cerebrospinal Fluid of Mumps Meningoencephalitic Children

Acta medica Iranica, 2009-10, Vol.47 (3), p.171-174

2009

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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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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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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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Genetics of intellectual disability in consanguineous families

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

2019

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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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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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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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Effect of inbreeding on intellectual disability revisited by trio sequencing

Risk factors of pediatric arterial ischemic stroke; A regional survey

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

Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism

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

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

Mitochondrial Copy Number and D-Loop Variants in Pompe Patients

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

Neurobrucellosis: A Partially Treatable Cause of Vision Loss

Investigation of microdeletions in syndromic intellectual disability by MLPA in Iranian population

Recurrence of Developmental and Epileptic Encephalopathy 9 (DEE9) in Two Siblings Due to Parental Germline Mosaicism of PCDH19 Mutation and Review of the Literature

Neurocognitive effects of phenobarbital discontinuation in epileptic children

HEREDITARY SPASTIC PARAPLEGIA: FROM GENE TO CLINIC

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

Specific Anti Mumps Antibodies (IgG IgM) in Cerebrospinal Fluid of Mumps Meningoencephalitic Children

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

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

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

Genetics of intellectual disability in consanguineous families

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

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

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

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