C Criscuolo, S Banfi, M Orio, P Gasparini, A Monticelli, V Scarano, F M Santorelli, A Perretti, L Santoro, G De Michele, A Filla. Neurology 2004
Times Cited: 58
Times Cited: 58
Isabelle Le Ber, Maria-Ceù Moreira, Sophie Rivaud-Péchoux, Céline Chamayou, François Ochsner, Thierry Kuntzer, Marc Tardieu, Gérard Saïd, Marie-Odile Habert, Geneviève Demarquay, Christian Tannier, Jean-Marie Beis, Alexis Brice, Michel Koenig, Alexandra Dürr. Brain 2003
Times Cited: 157
Times Cited: 157
List of shared articles
Times cited
[Clinical details and genetics of recessive ataxias].
C Zühlke, F Kreuz, K Bürk. Nervenarzt 2011
C Zühlke, F Kreuz, K Bürk. Nervenarzt 2011
Clinical features and molecular genetics of autosomal recessive cerebellar ataxias.
Brent L Fogel, Susan Perlman. Lancet Neurol 2007
Brent L Fogel, Susan Perlman. Lancet Neurol 2007
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients.
M Anheim, B Monga, M Fleury, P Charles, C Barbot, M Salih, J P Delaunoy, M Fritsch, L Arning, M Synofzik,[...]. Brain 2009
M Anheim, B Monga, M Fleury, P Charles, C Barbot, M Salih, J P Delaunoy, M Fritsch, L Arning, M Synofzik,[...]. Brain 2009
Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.
José Berciano, Antonio García, Jon Infante. Handb Clin Neurol 2013
José Berciano, Antonio García, Jon Infante. Handb Clin Neurol 2013
[Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology].
C Espinós-Armero, P González-Cabo, F Palau-Martínez. Rev Neurol 2005
C Espinós-Armero, P González-Cabo, F Palau-Martínez. Rev Neurol 2005
Clinical presentation and early evolution of spastic ataxia of Charlevoix-Saguenay.
Antoine Duquette, Bernard Brais, Jean-Pierre Bouchard, Jean Mathieu. Mov Disord 2013
Antoine Duquette, Bernard Brais, Jean-Pierre Bouchard, Jean Mathieu. Mov Disord 2013
Autosomal recessive cerebellar ataxias.
Francesc Palau, Carmen Espinós. Orphanet J Rare Dis 2006
Francesc Palau, Carmen Espinós. Orphanet J Rare Dis 2006