Publications by authors named "Marina Ferrone"

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ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementia.
Elisa Rubino, Cecilia Mancini, Silvia Boschi, Patrizia Ferrero, Marina Ferrone

Neurobiol Aging· January 2019

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Spinocerebellar Ataxia Tethering PCR: A Rapid Genetic Test for the Diagnosis of Spinocerebellar Ataxia Types 1, 2, 3, 6, and 7 by PCR and Capillary Electrophoresis.
Claudia Cagnoli, Alessandro Brussino, Cecilia Mancini, Marina Ferrone, Laura Orsi

J Mol Diagn· May 2018

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Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia.
Alessandro Brussino, Claudio Graziano, Dario Giobbe, Marina Ferrone, Elisa Dragone

Mov Disord· July 2010

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Mutations in the POLG1 gene are not a relevant cause of cerebellar ataxia in Italy.
Claudia Cagnoli, Alessandro Brussino, Eleonora Di Gregorio, Paola Caroppo, Silvia Stola, Marina Ferrone

J Neurol· July 2008

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Juvenile renal cell carcinoma as first manifestation of von Hippel-Lindau disease.
Antonio Granata, Adalberto Sessa, Marco Righetti, Sarah Cordaro, Giorgio Leone, Marina Ferrone

J Nephrol· October 2004

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