Detalhe da pesquisa
1.
The use of nerve and muscle biopsy in the diagnosis of vasculitis: a 5 year retrospective study.
J Neurol Neurosurg Psychiatry
; 79(12): 1376-81, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-18819942
2.
Amyotrophic lateral sclerosis in South-East England: a population-based study. The South-East England register for amyotrophic lateral sclerosis (SEALS Registry).
Neuroepidemiology
; 29(1-2): 44-8, 2007.
Artigo
em Inglês
| MEDLINE | ID: mdl-17898523
3.
Probabilistic diffusion tractography: a potential tool to assess the rate of disease progression in amyotrophic lateral sclerosis.
Brain
; 129(Pt 7): 1859-71, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16672290
4.
Antioxidant treatment for amyotrophic lateral sclerosis / motor neuron disease.
Cochrane Database Syst Rev
; (1): CD002829, 2007 Jan 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-17253482
5.
Effects of resistance training on myosin function studied by the in vitro motility assay in young and older men.
J Appl Physiol (1985)
; 98(6): 2390-5, 2005 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-15677736
6.
Antioxidant treatment for amyotrophic lateral sclerosis / motor neuron disease.
Cochrane Database Syst Rev
; (1): CD002829, 2005 Jan 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-15674899
7.
Clinical implications of the genetics of ALS and other motor neuron diseases.
Neurology
; 57(1): 9-17, 2001 Jul 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-11460829
8.
Definitive molecular diagnosis of facioscapulohumeral dystrophy.
Neurology
; 52(9): 1822-6, 1999 Jun 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-10371529
9.
Acanthocytosis, retinitis pigmentosa, and pallidal degeneration: a report of three patients, including the second reported case with hypoprebetalipoproteinemia (HARP syndrome).
Neurology
; 45(3 Pt 1): 487-92, 1995 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-7898702
10.
Clinical and functional investigation of 10 missense mutations and a novel frameshift insertion mutation of the gene for copper-zinc superoxide dismutase in UK families with amyotrophic lateral sclerosis.
Neurology
; 48(3): 746-51, 1997 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-9065559
11.
Amyotrophic lateral sclerosis: copper/zinc superoxide dismutase (SOD1) gene mutations.
Neuromuscul Disord
; 10(1): 63-8, 2000 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-10677867
12.
A case of severe congenital chronic inflammatory demyelinating polyneuropathy with complete spontaneous remission.
Neuromuscul Disord
; 14(12): 818-21, 2004 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-15564039
13.
Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis.
Neuromuscul Disord
; 6(5): 361-6, 1996 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-8938700
14.
Pseudotumour cerebri and paraproteinaemia.
Leuk Lymphoma
; 5(2-3): 211-3, 1991.
Artigo
em Inglês
| MEDLINE | ID: mdl-21269084
15.
Familial ALS is associated with mutations in all exons of SOD1: a novel mutation in exon 3 (Gly72Ser).
J Neurol Sci
; 153(1): 46-9, 1997 Dec 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-9455977
16.
Investigation of a null mutation of the CNTF gene in familial amyotrophic lateral sclerosis.
J Neurol Sci
; 132(2): 126-8, 1995 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-8543936
17.
The relationship of spinal muscular atrophy to motor neuron disease: investigation of SMN and NAIP gene deletions in sporadic and familial ALS.
J Neurol Sci
; 145(1): 55-61, 1997 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-9073029
18.
Clinical characteristics of SOD1 gene mutations in UK families with ALS.
J Neurol Sci
; 169(1-2): 56-60, 1999 Oct 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-10540008
19.
Antioxidant treatment for amyotrophic lateral sclerosis / motor neuron disease.
Cochrane Database Syst Rev
; (4): CD002829, 2004 Oct 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-15495036
20.
Myopathy in acquired partial lipodystrophy.
Clin Neurol Neurosurg
; 97(2): 181-6, 1995 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-7656496