Detalhe da pesquisa
1.
Differential expression of perforin in muscle-infiltrating T cells in polymyositis and dermatomyositis.
J Clin Invest
; 97(12): 2905-10, 1996 Jun 15.
Artigo
Inglês
| MEDLINE | ID: mdl-8675705
2.
LGMD 2I due to the common mutation 826C>A in the FKRP gene presenting as myopathy with vacuoles and paired-helical filaments.
Acta Myol
; 25(2): 73-6, 2006 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-18593008
3.
Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies.
J Med Genet
; 38(10): 665-73, 2001 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-11584044
4.
Milling precision and fitting accuracy of Cerec Scan milled restorations.
Int J Comput Dent
; 8(4): 273-81, 2005 Oct.
Artigo
Inglês, Alemão
| MEDLINE | ID: mdl-16689028
5.
Proximal myotonic myopathy. Clinical features of a multisystem disorder similar to myotonic dystrophy.
Arch Neurol
; 52(1): 25-31, 1995 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-7826272
6.
A placebo-controlled crossover trial of creatine in mitochondrial diseases.
Neurology
; 55(11): 1748-51, 2000 Dec 12.
Artigo
Inglês
| MEDLINE | ID: mdl-11113239
7.
Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts.
Neurology
; 44(8): 1448-52, 1994 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-8058147
8.
Creatine monohydrate in muscular dystrophies: A double-blind, placebo-controlled clinical study.
Neurology
; 54(9): 1848-50, 2000 May 09.
Artigo
Inglês
| MEDLINE | ID: mdl-10802796
9.
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin.
Neurology
; 53(7): 1564-9, 1999 Oct 22.
Artigo
Inglês
| MEDLINE | ID: mdl-10534268
10.
An inherited 4q35-EcoRI-DNA-fragment of 35 kb in a family with a sporadic case of facioscapulohumeral muscular dystrophy (FSHD).
Neuromuscul Disord
; 10(3): 178-81, 2000 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-10734264
11.
Chronic myopathy in a patient suspected of carrying two malignant hyperthermia susceptibility (MHS) mutations.
Neuromuscul Disord
; 2(5-6): 389-96, 1992.
Artigo
Inglês
| MEDLINE | ID: mdl-1300187
12.
Immunosuppressive treatment of rippling muscles in patients with myasthenia gravis.
Neuromuscul Disord
; 9(8): 604-7, 1999 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-10619721
13.
A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population.
Neuromuscul Disord
; 12(6): 558-65, 2002 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-12117480
14.
De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy.
Neuromuscul Disord
; 12(10): 947-51, 2002 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-12467750
15.
Fatal mitochondrial myopathy with cytochrome-c-oxidase deficiency and subunit-restricted reduction of enzyme protein in two siblings: an autopsy-immunocytochemical study.
Hum Pathol
; 20(7): 666-72, 1989 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-2472348
16.
Detection of humoral rejection in human cardiac allografts by assessing the capillary deposition of complement fragment C4d in endomyocardial biopsies.
J Heart Lung Transplant
; 18(9): 904-12, 1999 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-10528753
17.
Adult human cardiomyocytes coexpress vimentin and Ki67 in heart transplant rejection and in dilated cardiomyopathy.
J Heart Lung Transplant
; 17(8): 795-800, 1998 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-9730429
18.
Type 2a fibre rhabdomyolysis in myoadenylate deaminase deficiency.
J Neurol
; 238(1): 31-3, 1991 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-2030369
19.
Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes.
J Neurol
; 237(1): 5-10, 1990 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-2156958
20.
Magnetic resonance imaging of skeletal muscles in idiopathic inflammatory myopathies of adults.
J Neurol
; 241(5): 306-14, 1994 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-8006684