Barbara Gandolfi < Barbara Garavaglia < Barbara Giovannone

Facettes :

List of bibliographic references indexed by Barbara Garavaglia

Number of relevant bibliographic references: 3.

Ident.	Authors (with country if any)	Title
000D20 (2008)	Roberta Marongiu [Italie] ; Alessandro Ferraris [Italie] ; Tàmara Ialongo [Italie] ; Silvia Michiorri [Italie] ; Francesco Soleti [Italie] ; Francesca Ferrari [Italie] ; Antonio E. Elia [Italie] ; Daniele Ghezzi [Italie] ; Alberto Albanese [Italie] ; Maria Concetta Altavista [Italie] ; Angelo Antonini [Italie] ; Paolo Barone [Italie] ; Livia Brusa [Italie] ; Pietro Cortelli [Italie] ; Paolo Martinelli [Italie] ; Maria Teresa Pellecchia [Italie] ; Gianni Pezzoli [Italie] ; Cesa Scaglione [Italie] ; Paolo Stanzione [Italie] ; Michele Tinazzi [Italie] ; Anna Zecchinelli [Italie] ; Massimo Zeviani [Italie] ; Emanuele Cassetta [Italie] ; Barbara Garavaglia [Italie] ; Bruno Dallapiccola [Italie] ; Anna Rita Bentivoglio [Italie] ; Enza Maria Valente [Italie]	PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrum
000D64 (2008)	Vania Gelmetti [Italie] ; Alessandro Ferraris [Italie] ; Livia Brusa [Italie] ; Francesca Romano [Italie] ; Federica Lombardi [Italie] ; Chiara Barzaghi [Italie] ; Paolo Stanzione [Italie] ; Barbara Garavaglia [Italie] ; Bruno Dallapiccola [Italie] ; Enza Maria Valente [Italie]	Late onset sporadic Parkinson's disease caused by PINK1 mutations: Clinical and functional study
001001 (2007)	Francesca Del Sorbo [Italie] ; Antonio E. Elia [Italie] ; Gabriella De Joanna [Italie] ; Luigi M. Romito [Italie] ; Barbara Garavaglia [Italie] ; Alberto Albanese [Italie]	Normal cardiovascular reflex testing in patients with parkin disease

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List of associated KwdEn.i

Nombre de documents	Descripteur
2	PINK1
2	autosomal recessive parkinsonism
1	Parkinson disease
1	Parkinson's disease
1	TUNEL assay
1	apoptosis
1	autonomic nervous system
1	cardiovascular reflex test
1	dysautonomia
1	heterozygous rare variants
1	late onset
1	orthostatic hypotension
1	parkin disease

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