C. Salvador < C. Sampaio < C. Sands

Facettes :

List of bibliographic references indexed by C. Sampaio

Number of relevant bibliographic references: 3.

Ident.	Authors (with country if any)	Title
001206 (2006)	M. Horstink [Pays-Bas] ; E. Tolosa [Espagne] ; U. Bonuccelli [Italie] ; G. Deuschl [Allemagne] ; A. Friedman [Pologne] ; P. Kanovsky [République tchèque] ; J. P. Larsen [Norvège] ; A. Lees [Royaume-Uni] ; W. Oertel [Allemagne] ; Werner Poewe [Autriche] ; Olivier Rascol [France] ; C. Sampaio [Portugal]	Review of the therapeutic management of Parkinson's disease. Report of a joint task force of the European Federation of Neurological Societies and the Movement Disorder Society–European Section. Part I: early (uncomplicated) Parkinson's disease
001207 (2006)	M. Horstink [Pays-Bas] ; E. Tolosa [Espagne] ; U. Bonuccelli [Italie] ; G. Deuschl [Allemagne] ; A. Friedman [Pologne] ; P. Kanovsky [République tchèque] ; J. P. Larsen [Norvège] ; A. Lees [Royaume-Uni] ; W. Oertel [Allemagne] ; Werner Poewe [Autriche] ; Olivier Rascol [France] ; C. Sampaio [Portugal]	Review of the therapeutic management of Parkinson's disease. Report of a joint task force of the European Federation of Neurological Societies (EFNS) and the Movement Disorder Society‐European Section (MDS‐ES). Part II: late (complicated) Parkinson's disease
001408 (2005)	S. Goldwurm [Italie] ; A Di Fonzo [Italie] ; E J Simons [Pays-Bas] ; C F Rohé [Pays-Bas] ; M. Zini [Italie] ; M. Canesi [Italie] ; S. Tesei [Italie] ; A. Zecchinelli [Italie] ; A. Antonini [Italie] ; C. Mariani [Italie] ; N. Meucci [Italie] ; G. Sacilotto [Italie] ; F. Sironi [Italie] ; G. Salani [Italie] ; J. Ferreira [Portugal] ; H F Chien [Brésil] ; E. Fabrizio [Italie] ; N. Vanacore [Italie] ; A Dalla Libera [Italie] ; F. Stocchi [Italie] ; C. Diroma [Italie] ; P. Lamberti [Italie] ; C. Sampaio [Portugal] ; G. Meco [Italie] ; E. Barbosa [Brésil] ; A M Bertoli-Avella [Pays-Bas] ; G J Breedveld [Pays-Bas] ; B A Oostra [Pays-Bas] ; G. Pezzoli [Italie] ; V. Bonifati [Pays-Bas]	The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson’s disease and originates from a common ancestor

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List of associated KwdEn.i

Nombre de documents	Descripteur
2	Parkinson's disease
2	management guideline
2	pharmacotherapy
2	review
1	G2019S
1	LD, linkage disequilibrium
1	LRRK2
1	Parkinson’s disease
1	SNP, single nucleotide polymorphism
1	founder
1	mutation
1	neurosurgery
1	physiotherapy

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