Pesquisa | BVS Doenças Infecciosas e Parasitárias

1.

Non-motor symptoms burden in treated and untreated early Parkinson's disease patients: argument for non-motor subtypes.

Zis, P; Martinez-Martin, P; Sauerbier, A; Rizos, A; Sharma, J C; Worth, P F; Sophia, R; Silverdale, M; Chaudhuri, K Ray.

Eur J Neurol ; 22(8): 1145-50, 2015 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-25981492

2.

Adherence therapy improves medication adherence and quality of life in people with Parkinson's disease: a randomised controlled trial.

Daley, D J; Deane, K H O; Gray, R J; Clark, A B; Pfeil, M; Sabanathan, K; Worth, P F; Myint, P K.

Int J Clin Pract ; 68(8): 963-71, 2014 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-24750544

3.

Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia.

Worth, P F; Houlden, H; Giunti, P; Davis, M B; Wood, N W.

Nat Genet ; 24(3): 214-5, 2000 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-10700168

4.

Spinocerebellar ataxia type 12 is rare in the United Kingdom.

Worth, P F; Wood, N W.

Neurology ; 56(3): 419-20, 2001 Feb 13.

Artigo em Inglês | MEDLINE | ID: mdl-11171918

5.

Spinocerebellar ataxia type 11.

Giunti, P; Houlden, H; Gardner-Thorpe, C; Worth, P F; Johnson, J; Hilton, D A; Revesz, T; Davis, M B; Wood, N W.

Handb Clin Neurol ; 103: 521-34, 2012.

Artigo em Inglês | MEDLINE | ID: mdl-21827911

6.

Syncope associated with pain as the presenting feature of neck malignancy: failure of cardiac pacemaker to prevent attacks in two cases.

Worth, P F; Stevens, J C; Lasri, F; Brew, S; Reilly, M M; Mathias, C J; Rudge, P.

J Neurol Neurosurg Psychiatry ; 76(9): 1301-3, 2005 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-16107374

7.

Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutation.

Giunti, P; Stevanin, G; Worth, P F; David, G; Brice, A; Wood, N W.

Am J Hum Genet ; 64(6): 1594-603, 1999 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-10330346

8.

Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3.

Worth, P F; Giunti, P; Gardner-Thorpe, C; Dixon, P H; Davis, M B; Wood, N W.

Am J Hum Genet ; 65(2): 420-6, 1999 Aug.

Artigo em Inglês | MEDLINE | ID: mdl-10417284

9.

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.

Sinha, K K; Worth, P F; Jha, D K; Sinha, S; Stinton, V J; Davis, M B; Wood, N W; Sweeney, M G; Bhatia, K P.

J Neurol Neurosurg Psychiatry ; 75(3): 448-52, 2004 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-14966163

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