Detalhe da pesquisa
1.
Extending and outlining the genotypic and phenotypic spectrum of novel mutations of NALCN gene in IHPRF1 syndrome: identifying recurrent urinary tract infection.
Neurol Sci
; 44(12): 4491-4498, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37452996
2.
Motor planning is not restricted to only one hemisphere: evidence from ERPs in individuals with hemiplegic cerebral palsy.
Exp Brain Res
; 240(9): 2311-2326, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35876852
3.
Identification of novel mutations among Iranian NPC1 patients: a bioinformatics approach to predict pathogenic mutations.
Hereditas
; 159(1): 8, 2022 Jan 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35086560
4.
Genetics of intellectual disability in consanguineous families.
Mol Psychiatry
; 24(7): 1027-1039, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29302074
5.
Knowledge, attitudes, and practices among mothers of children with epilepsy: A study in a teaching hospital.
Epilepsy Behav
; 69: 147-152, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28285235
6.
Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group.
BMC Neurol
; 15: 205, 2015 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26471939
7.
Megaconial congenital muscular dystrophy due to CHKB gene variants, the first report of thirteen Iranian patients.
Neuromuscul Disord
; 33(7): 589-595, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37393748
8.
A novel mutation in MCPH1 gene in an Iranian family with primary microcephaly.
J Pak Med Assoc
; 62(11): 1244-7, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23866422
9.
Analysis of the HEXA, HEXB, ARSA, and SMPD1 Genes in 68 Iranian Patients.
J Mol Neurosci
; 72(3): 555-564, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34554397
10.
Five patients with spinal muscular atrophy-progressive myoclonic epilepsy (SMA-PME): a novel pathogenic variant, treatment and review of the literature.
Neuromuscul Disord
; 32(10): 806-810, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36309462
11.
Epidemiology of Guillain-Barré Syndrome in Iranian Children Aged 0-15 Years (2008-2013).
Iran J Child Neurol
; 15(4): 27-34, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34782839
12.
Recurrent angioedema, Guillain-Barré, and myelitis in a girl with systemic lupus erythematosus and CD59 deficiency syndrome.
Auto Immun Highlights
; 11(1): 9, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32612799
13.
Prediction of Response to Treatment in Children with Epilepsy.
Iran J Child Neurol
; 12(3): 94-100, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30026773
14.
Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome.
Eur J Med Genet
; 61(10): 585-595, 2018 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-29605658
15.
Glutaric AciduriaType 1: Clinical and Molecular Study in Iranian Patients, 3 Novel Mutations.
Iran J Child Neurol
; 11(4): 58-65, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29201125
16.
Another Limping Child: An Interesting Diagnosis Journey.
Iran J Child Neurol
; 11(4): 71-76, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-29201127
17.
Clinical and Epidemiological Aspects of Multiple Sclerosis in Children.
Iran J Child Neurol
; 11(2): 37-43, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28698726
18.
Exploring the Psychometric Properties of the Farsi Version of Quality of Life Kindl Questionnaire for 4-7 Year-Old Children in Iran.
Iran J Child Neurol
; 10(2): 42-52, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27247583
19.
Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic Group.
J Mol Neurosci
; 59(3): 392-6, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27262448
20.
Comparative efficacy of zonisamide and pregabalin as an adjunctive therapy in children with refractory epilepsy.
Iran J Child Neurol
; 9(1): 49-55, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25767539