C. Maragoto < C. Mariani < C. Marin

Facettes :

List of bibliographic references indexed by C. Mariani

Number of relevant bibliographic references: 4.

Ident.	Authors (with country if any)	Title
000315 (2011)	B. Borroni ; S. Goldwurm [Italie] ; C. Cerini ; M. Cosseddu ; N. Meucci [Italie] ; C. Mariani [Italie] ; G. Pezzoli [Italie] ; A. Padovani	Familial aggregation in Progressive Supranuclear Palsy and Corticobasal Syndrome
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
001B74 (2000)	E. Farina [Italie] ; G. Gattellaro [Italie] ; S. Pomati [Italie] ; E. Magni [Italie] ; A. Perretti [Italie] ; A. P. Cannatà [Italie] ; P. Nichelli [Italie] ; C. Mariani [Italie]	Researching a differential impairment of frontal functions and explicit memory in early Parkinson’s disease
002439 (1994)	E. Farina ; S. F. Cappa [Italie] ; M. Polimeni ; E. Magni [Italie] ; M. Canesi ; A. Zecchinelli ; G. Scarlato ; C. Mariani	Frontal dysfunction in early Parkinson's diseases

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List of associated KwdEn.i

Nombre de documents	Descripteur
2	Parkinson’s disease
1	G2019S
1	LD, linkage disequilibrium
1	LRRK2
1	Parkinson's disease
1	SNP, single nucleotide polymorphism
1	anticholinergics
1	cognitive disorders and dementia
1	explicit memory
1	founder
1	frontal function
1	frontal functions
1	frontotemporal dementia
1	movement disorders
1	mutation
1	neurodegenerative
1	neurological disorders
1	progressive supranuclear palsy

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