Researcher
Cinzia Gellera
Fondazione IRCCS Istituto Neurologico Carlo Besta
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127 papers found
All papers authored by Cinzia Gellera
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M. Ermani,
E. Pegoraro,
C. Mariotti,
C. Gellera ,
M. G. Hanna,
D. Pareyson,
P. Fratta
and 1 other authors
No effect ofARpolyG polymorphism on spinal and bulbar muscular atrophy phenotype
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Simon Topp ,
Shu Yang,
Bradley Smith,
Jennifer A. Fifita,
Sadaf T. Warraich,
Katharine Y. Zhang,
Natalie Farrawell,
Marka van Blitterswijk,
Caroline Vance ,
Xun Hu,
Alessandra Chesi,
Claire S. Leblond,
Albert Lee ,
Stephanie L. Rayner
and 55 other authors
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
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Mirella Filocamo,
Alessandro Padovani
Download from www.ncbi.nlm.nih.gov
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V. Pensato,
D. Cazzato,
G. Lauria
Amyotrophic lateral sclerosis causes small fiber pathology
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J. Lyahyai,
Y. Kriouile,
A. Sefiani
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,
Davide Pareyson
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,
Jun Li,
Stephan Züchner,
Stephan Z?chner,
Caterina Mariotti
and 4 other authors
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Federica Natacci,
Luigina Spaccini,
Serena Gasperini,
Frédéric M. Vaz,
David N. Cooper,
Renzo Guerrini,
Amelia Morrone
Download from www.nature.com
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Stefania Elena Navone,
Giovanni Marfia,
Giulio Alessandri,
Fabio Corsi,
Eugenio Agostino Parati
and 2 other authors
Human Adipose-Derived Mesenchymal Stem Cells as a New Model of Spinal and Bulbar Muscular Atrophy
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Lh van den Berg,
Nicola Ticozzi ,
Claudia Fallini,
As Gkazi,
Simon Topp ,
Kp Kenna,
El Scotter ,
Jw Miller,
Jason Kost,
Ew Danielson,
Pamela Keagle,
Ea Lewis,
Daniela Calini,
Anneloor Lma Ten Asbroek
and 80 other authors
Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS.
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Serena Caldarazzo,
Morten Duno,
Maria Soller,
Andreas Puschmann
Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis
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Davide Pareyson,
Claudia Ciano,
Lorenzo Nanetti,
Ettore Salsano,
Giuseppe Piscosquito,
Elisa Sarto,
Marica Eoli,
Isabella Moroni,
Paola Soliveri,
Elena Lamperti,
Luisa Chiapparini,
Daniela Di Bella
and 2 other authors
Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48
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Cinzia Gellera ,
Antonia Ratti,
Franco Taroni,
Adriano Chio,
Andrea Calvo,
Gabriele Mora,
Gabriella Restagno,
Bryan J. Traynor,
Anna Birve,
Robin Lemmens,
Michael A. van Es,
Christiaan G. J. Saris
and 30 other authors
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
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