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Showing results (31-40 of 43) with videos related to

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Annals of Human Genetics|September 1, 1996
Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansionsM Frontali, G Sabbadini, A Novelletto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 16, 2015
A panel of nine cerebrospinal fluid biomarkers may identify patients with atypical parkinsonian syndromesN K Magdalinou, R W Paterson, J M Schott, et al.
Nature Genetics|September 1, 1997
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansionG David, N Abbas, G Stevanin, et al.
European Neurology|November 14, 2012
Prospective analysis of falls in dominant ataxiasE M R Fonteyn, T Schmitz-Hübsch, C C P Verstappen, et al.
Cerebellum (London, England)|October 24, 2012
Inventory of Non-Ataxia Signs (INAS): validation of a new clinical assessment instrumentH Jacobi, M Rakowicz, R Rola, et al.
Neurology|October 12, 2005
Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variationN P Davies, P Imbrici, D Fialho, et al.
Neurology|February 24, 2010
Responsiveness of different rating instruments in spinocerebellar ataxia patientsT Schmitz-Hübsch, R Fimmers, M Rakowicz, et al.
Neurology|June 14, 2006
Scale for the assessment and rating of ataxia: development of a new clinical scaleT Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, et al.
Neurology|August 13, 2008
SCA Functional Index: a useful compound performance measure for spinocerebellar ataxiaT Schmitz-Hübsch, P Giunti, D A Stephenson, et al.
Brain : a Journal of Neurology|June 11, 2005
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study GroupC Kamm, D G Healy, N P Quinn, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Annals of Human Genetics|September 1, 1996
Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansionsM Frontali, G Sabbadini, A Novelletto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 16, 2015
A panel of nine cerebrospinal fluid biomarkers may identify patients with atypical parkinsonian syndromesN K Magdalinou, R W Paterson, J M Schott, et al.
Nature Genetics|September 1, 1997
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansionG David, N Abbas, G Stevanin, et al.
European Neurology|November 14, 2012
Prospective analysis of falls in dominant ataxiasE M R Fonteyn, T Schmitz-Hübsch, C C P Verstappen, et al.
Cerebellum (London, England)|October 24, 2012
Inventory of Non-Ataxia Signs (INAS): validation of a new clinical assessment instrumentH Jacobi, M Rakowicz, R Rola, et al.
Neurology|October 12, 2005
Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variationN P Davies, P Imbrici, D Fialho, et al.
Neurology|February 24, 2010
Responsiveness of different rating instruments in spinocerebellar ataxia patientsT Schmitz-Hübsch, R Fimmers, M Rakowicz, et al.
Neurology|June 14, 2006
Scale for the assessment and rating of ataxia: development of a new clinical scaleT Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, et al.
Neurology|August 13, 2008
SCA Functional Index: a useful compound performance measure for spinocerebellar ataxiaT Schmitz-Hübsch, P Giunti, D A Stephenson, et al.
Brain : a Journal of Neurology|June 11, 2005
The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study GroupC Kamm, D G Healy, N P Quinn, et al.
Pageof 5