Detalhe da pesquisa
1.
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.
Am J Hum Genet
; 96(6): 992-1000, 2015 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26046367
2.
The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations.
Epilepsy Behav
; 68: 103-107, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28142128
3.
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.
Nat Genet
; 39(6): 721-3, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17529978
4.
Copy number variations and susceptibility to lateral temporal epilepsy: a study of 21 pedigrees.
Epilepsia
; 55(10): 1651-8, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25243798
5.
Molecular changes induced by the curcumin analogue D6 in human melanoma cells.
Mol Cancer
; 12: 37, 2013 May 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23642048
6.
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.
Epilepsia
; 54(7): 1288-97, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23621105
7.
FCGR3B copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans.
Rheumatology (Oxford)
; 50(7): 1206-10, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21296850
8.
Association of variation in Fcgamma receptor 3B gene copy number with rheumatoid arthritis in Caucasian samples.
Ann Rheum Dis
; 69(9): 1711-6, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20472591
9.
Microsatellites and SNPs linkage analysis in a Sardinian genetic isolate confirms several essential hypertension loci previously identified in different populations.
BMC Med Genet
; 10: 81, 2009 Aug 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-19715579
10.
Suggestive linkage of familial mesial temporal lobe epilepsy to chromosome 3q26.
Epilepsy Res
; 108(2): 232-40, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24315020
11.
Identification of a PKP2 gene deletion in a family with arrhythmogenic right ventricular cardiomyopathy.
Eur J Hum Genet
; 21(11): 1226-31, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23486541
12.
Ocular refraction: heritability and genome-wide search for eye morphometry traits in an isolated Sardinian population.
Hum Genet
; 116(3): 152-9, 2005 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-15611866
13.
A new essential hypertension susceptibility locus on chromosome 2p24-p25, detected by genomewide search.
Am J Hum Genet
; 71(4): 893-905, 2002 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-12228842