Detalhe da pesquisa
1.
FUT2: filling the gap between genes and environment in Behçet's disease?
Ann Rheum Dis
; 74(3): 618-24, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24326010
2.
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.
Nat Genet
; 37(3): 289-94, 2005 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15731758
3.
Association study of IL10 and IL23R-IL12RB2 in Iranian patients with Behçet's disease.
Arthritis Rheum
; 64(8): 2761-72, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22378604
4.
Kalirin: a novel genetic risk factor for ischemic stroke.
Hum Genet
; 127(5): 513-23, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20107840
5.
Variants of the Matrix Metalloproteinase-2 but not the Matrix Metalloproteinase-9 genes significantly influence functional outcome after stroke.
BMC Med Genet
; 11: 40, 2010 Mar 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-20222942
6.
Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke: a case-control, meta-analysis and functional study.
Cerebrovasc Dis
; 29(6): 528-37, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20357438
7.
Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.
BMC Med Genet
; 9: 57, 2008 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-18593462
8.
IL10 low-frequency variants in Behçet's disease patients.
Int J Rheum Dis
; 20(5): 622-627, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24708170
9.
Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet's disease susceptibility.
Nat Genet
; 49(3): 438-443, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28166214
10.
Association of mitochondrial polymorphism m.709G>A with Behçet's disease.
Ann Rheum Dis
; 70(8): 1514-6, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21345811
11.
Mitochondrial genome association study with peripheral arterial disease and venous thromboembolism.
Atherosclerosis
; 252: 97-105, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27513348
12.
Ulcerative Colitis Is Under Dual (Mitochondrial and Nuclear) Genetic Control.
Inflamm Bowel Dis
; 22(4): 774-81, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26926037
13.
Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax.
PLoS One
; 11(5): e0156103, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27203581
14.
Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.
Neurology
; 86(13): 1217-26, 2016 Mar 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-26935894
15.
Effect of hydration variability on hybrid layer properties of a self-etching versus an acid-etching system.
Biomaterials
; 26(9): 1011-8, 2005 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15369689
16.
Brief report: association of CCR1, KLRC4, IL12A-AS1, STAT4, and ERAP1 With Behçet's disease in Iranians.
Arthritis Rheumatol
; 67(10): 2742-8, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26097239
17.
Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal.
PLoS One
; 10(7): e0133422, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-26186006
18.
Characterization of the major histocompatibility complex locus association with Behçet's disease in Iran.
Arthritis Res Ther
; 17: 81, 2015 Mar 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25889189
19.
Association study of Parkin gene polymorphisms with idiopathic Parkinson disease.
Arch Neurol
; 60(7): 975-80, 2003 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-12873854
20.
The Q7R Saitohin gene polymorphism is not associated with Alzheimer disease.
Neurosci Lett
; 347(3): 143-6, 2003 Aug 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-12875906