Detalhe da pesquisa
1.
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population.
Hum Genomics
; 18(1): 35, 2024 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38570878
2.
A comparative study on prophylactic efficacy of cinnarizine and amitriptyline in childhood migraine: a randomized double-blind clinical trial.
Cephalalgia
; 44(4): 3331024241230963, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38641932
3.
Distinct neurological phenotypes associated with biallelic loss of NOTCH3 function: evidence for recessive inheritance.
Mol Biol Rep
; 51(1): 714, 2024 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38824264
4.
Expanding the neuroimaging findings of guanidinoacetate methyltransferase deficiency in an Iranian girl with a homozygous frameshift variant in the GAMT.
Neurogenetics
; 24(2): 67-78, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36633690
5.
High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Neurogenetics
; 24(4): 279-289, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37597066
6.
Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra.
Cerebellum
; 22(4): 640-650, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35731353
7.
Efficacy and safety of miglustat in the treatment of GM2 gangliosidosis: A systematic review.
Eur J Neurol
; 30(9): 2919-2945, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37209042
8.
ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variants.
Hum Genomics
; 15(1): 45, 2021 07 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-34281620
9.
Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy.
BMC Neurol
; 22(1): 162, 2022 May 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35501714
10.
The safety and efficacy of umbilical cord blood mononuclear cells in individuals with spastic cerebral palsy: a randomized double-blind sham-controlled clinical trial.
BMC Neurol
; 22(1): 123, 2022 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-35351020
11.
The quality of life in children with spinal muscular atrophy: a case-control study.
BMC Pediatr
; 22(1): 708, 2022 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36503502
12.
The correlation between spiritual care competence and spiritual health among Iranian nurses.
BMC Nurs
; 21(1): 277, 2022 Oct 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36224620
13.
Developing new quantitative CT image markers to predict prognosis of acute ischemic stroke patients.
J Xray Sci Technol
; 30(3): 459-475, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35213340
14.
Developing a charter of spiritual care for patients.
Int J Qual Health Care
; 33(1)2021 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-33367741
15.
A novel pathogenic variant of BRAT1 gene causes rigidity and multifocal seizure syndrome, lethal neonatal.
Int J Neurosci
; 131(9): 875-878, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32345087
16.
Cinnarizine and sodium valproate as the preventive agents of pediatric migraine: A randomized double-blind placebo-controlled trial.
Cephalalgia
; 40(7): 665-674, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31707814
17.
Levetiracetam for prophylactic treatment of pediatric migraine: A randomized double-blind placebo-controlled trial.
Cephalalgia
; 39(12): 1509-1517, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31154809
18.
Correction to: High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry.
Neurogenetics
; 24(4): 317-318, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37668767
19.
The volume of fluid injected into the tissue expander and the tissue expansion.
J Res Med Sci
; 19(12): 1163-6, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25709658
20.
Homozygous TREM2 c.549del; p.(Leu184Serfs*5) variant causing Nasu-Hakola disease in three siblings in a consanguineous Iraqi family: Case report and review of literature.
Mol Genet Genomic Med
; 12(6): e2476, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38888203