Detalhe da pesquisa
1.
Protein- and mRNA-based phenotype-genotype correlations in DMD/BMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD gene.
Hum Mutat
; 28(2): 183-95, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17041906
2.
Phase I study of dystrophin plasmid-based gene therapy in Duchenne/Becker muscular dystrophy.
Hum Gene Ther
; 15(11): 1065-76, 2004 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-15610607
3.
Looking under every rock: Duchenne muscular dystrophy and traditional Chinese medicine.
Neuromuscul Disord
; 13(9): 705-7, 2003 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-14561492
4.
Dystrophinopathy caused by mid-intronic substitutions activating cryptic exons in the DMD gene.
Neuromuscul Disord
; 14(1): 10-8, 2004 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-14659407
5.
The role of muscle biopsy in analysis of the dystrophin gene in Duchenne muscular dystrophy: experience of a national referral centre.
Neuromuscul Disord
; 14(10): 650-8, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15351422
6.
82nd ENMC international workshop, 5th international Emery-Dreifuss muscular dystrophy (EDMD) workshop, 1st Workshop of the MYO-CLUSTER project EUROMEN (European muscle envelope nucleopathies), 15-16 September 2000, Naarden, The Netherlands.
Neuromuscul Disord
; 12(2): 187-94, 2002 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-11738362
7.
X-linked Emery-Dreifuss muscular dystrophy and vacuoles: an immunohistochemical characterization.
Muscle Nerve
; 32(1): 61-5, 2005 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15880484
8.
Skewed X-chromosome inactivation pattern in SRY positive XX maleness: a case report and review of literature.
Ann Genet
; 46(1): 11-8, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-12818524