Detalhe da pesquisa
1.
RFC1 expansions are a common cause of idiopathic sensory neuropathy.
Brain;
144(5): 1542-1550, 2021 06 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33969391
2.
Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome.
J Inherit Metab Dis;
39(5): 697-704, 2016 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-27106217
3.
Quality in molecular biology testing for inherited thrombophilia disorders.
Semin Thromb Hemost;
38(6): 600-12, 2012 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22907670
4.
Glycogen storage disease type III in the Irish population.
J Inherit Metab Dis;
33 Suppl 3: S215-8, 2010 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20490926
5.
Cardiac ankyrin repeat protein (CARP) expression in human and murine atherosclerotic lesions: activin induces CARP in smooth muscle cells.
Arterioscler Thromb Vasc Biol;
23(1): 64-8, 2003 Jan 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12524226
6.
The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population.
Br J Haematol;
125(5): 647-54, 2004 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15147381
7.
Gene expression profiling of resting and activated vascular smooth muscle cells by serial analysis of gene expression and clustering analysis.
Genomics;
82(3): 288-99, 2003 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12906854
8.
Inherited protein S deficiency: from genotype to phenotype.
Haematologica;
88(4): 363-7, 2003 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-12681962