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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 expansions
M 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 syndromes
N 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 expansion
G David, N Abbas, G Stevanin, et al.
European Neurology
|
November 14, 2012
Prospective analysis of falls in dominant ataxias
E 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 instrument
H Jacobi, M Rakowicz, R Rola, et al.
Neurology
|
October 12, 2005
Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation
N P Davies, P Imbrici, D Fialho, et al.
Neurology
|
February 24, 2010
Responsiveness of different rating instruments in spinocerebellar ataxia patients
T 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 scale
T Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, et al.
Neurology
|
August 13, 2008
SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia
T 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 Group
C Kamm, D G Healy, N P Quinn, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 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 expansions
M 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 syndromes
N 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 expansion
G David, N Abbas, G Stevanin, et al.
European Neurology
|
November 14, 2012
Prospective analysis of falls in dominant ataxias
E 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 instrument
H Jacobi, M Rakowicz, R Rola, et al.
Neurology
|
October 12, 2005
Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation
N P Davies, P Imbrici, D Fialho, et al.
Neurology
|
February 24, 2010
Responsiveness of different rating instruments in spinocerebellar ataxia patients
T 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 scale
T Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, et al.
Neurology
|
August 13, 2008
SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia
T 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 Group
C Kamm, D G Healy, N P Quinn, et al.
Page
of 5