Detalhe da pesquisa
1.
Welander distal myopathy is caused by a mutation in the RNA-binding protein TIA1.
Ann Neurol
; 73(4): 500-9, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23401021
2.
Intragenic deletion of TRIM32 in compound heterozygotes with sarcotubular myopathy/LGMD2H.
Hum Mutat
; 30(9): E831-44, 2009 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19492423
3.
Safety and tolerability of NXY-059 for acute intracerebral hemorrhage: the CHANT Trial.
Stroke
; 38(8): 2262-9, 2007 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-17569876
4.
Welander distal myopathy outside the Swedish population: phenotype and genotype.
Neuromuscul Disord
; 12(6): 544-7, 2002 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12117477
5.
Kinetic analysis and test-retest variability of the radioligand [11C](R)-PK11195 binding to TSPO in the human brain - a PET study in control subjects.
EJNMMI Res
; 2: 15, 2012 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-22524272
6.
Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus.
Neurogenetics
; 4(4): 173-7, 2003 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-12836053