Detalhe da pesquisa
1.
ANXA1 with Anti-Inflammatory Properties Might Contribute to Parkinsonism.
Ann Neurol
; 90(2): 319-323, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34180078
2.
PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism.
Mov Disord
; 32(2): 287-291, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27753167
3.
A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.
J Neural Transm (Vienna)
; 123(3): 323-8, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26354101
4.
The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson's disease in Iranian population.
Neurol Sci
; 37(5): 731-6, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26732583
5.
A Clinical and Molecular Genetic Study of 50 Families with Autosomal Recessive Parkinsonism Revealed Known and Novel Gene Mutations.
Mol Neurobiol
; 55(4): 3477-3489, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28502045
6.
RIT2 Polymorphisms: Is There a Differential Association?
Mol Neurobiol
; 54(3): 2234-2240, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26941103
7.
SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study.
J Neurol Sci
; 369: 1-4, 2016 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27653855
8.
Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population.
Genet Test Mol Biomarkers
; 20(10): 629-632, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27612022
9.
SNAP-25 gene variations and attention-deficit hyperactivity disorder in Iranian population.
Neurol Res
; 38(11): 959-964, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27627841
10.
c.376G>A mutation in WFS1 gene causes Wolfram syndrome without deafness.
Eur J Med Genet
; 59(2): 65-9, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26773575
11.
Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population.
J Neurol Sci
; 355(1-2): 72-4, 2015 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26070653
12.
A Novel PKD1 Mutation in a Patient with Autosomal Dominant Polycystic Kidney Disease.
Int J Mol Cell Med
; 5(2): 123-4, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27478809