Pieter Voorn < Pietro Cortelli < Pietro Delise

Facettes :

List of bibliographic references indexed by Pietro Cortelli

Number of relevant bibliographic references: 3.

Ident.	Authors (with country if any)	Title
000C01 (2008)	Giovanni Rizzo [Italie] ; Paolo Martinelli [Italie] ; David Manners [Italie] ; Cesa Scaglione [Italie] ; Caterina Tonon [Italie] ; Pietro Cortelli [Italie] ; Emil Malucelli [Italie] ; Sabina Capellari [Italie] ; Claudia Testa [Italie] ; Piero Parchi [Italie] ; Pasquale Montagna [Italie] ; Bruno Barbiroli [Italie] ; Raffaele Lodi [Italie]	Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease
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
001A34 (2001)	Anna R. Bentivoglio [Italie] ; Pietro Cortelli [Italie] ; Enza M. Valente [Italie] ; Tàmara Ialongo [Italie] ; Alessandro Ferraris [Italie] ; Antonio Elia [Italie] ; Pasquale Montagna [Italie] ; Alberto Albanese [Italie]	Phenotypic characterisation of autosomal recessive PARK6‐linked parkinsonism in three unrelated Italian families

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List of associated KwdEn.i

Nombre de documents	Descripteur
2	autosomal recessive parkinsonism
1	PARK6
1	PINK1
1	Parkinson disease
1	Parkinson's disease
1	early onset
1	family study
1	genetics
1	heterozygous rare variants

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