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G Stevanin

Showing results (1-10 of 81) with videos related to

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European Journal of Human Genetics : EJHG|March 14, 2000
Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathologyG Stevanin, A Dürr, A Brice
Revue Neurologique|May 27, 2015
Clinical and genetic heterogeneity in hereditary spastic paraplegias: from SPG1 to SPG72 and still countingS Klebe, G Stevanin, C Depienne
Revue Neurologique|April 29, 2017
Hereditary spastic paraplegia: More than an upper motor neuron diseaseL Parodi, S Fenu, G Stevanin, et al.
Neurology|October 16, 1999
Clinical and MRI findings in spinocerebellar ataxia type 5G Stevanin, A Herman, A Brice, et al.
Neurology|September 15, 2004
Mutations in the FGF14 gene are not a major cause of spinocerebellar ataxia in CaucasiansG Stevanin, A Durr, C Dussert, et al.
Revue Neurologique|May 7, 2011
Autosomal dominant cerebellar ataxiasC Marelli, C Cazeneuve, A Brice, et al.
Neurology|November 1, 1993
Familial essential tremor and idiopathic torsion dystonia are different genetic entitiesA Dürr, G Stevanin, C P Jedynak, et al.
Acta Neurologica Scandinavica. Supplementum|June 18, 2008
SPG11--the most common type of recessive spastic paraplegia in Norway?A K Erichsen, G Stevanin, P Denora, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1997
Saccade velocity in idiopathic and autosomal dominant cerebellar ataxiaK Bürk, M Fetter, M Skalej, et al.
American Journal of Human Genetics|May 20, 1999
Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutationP Giunti, G Stevanin, P F Worth, et al.
Pageof 9

Showing results (1-10 of 81) with videos related to

Sort By:
Pageof 9
European Journal of Human Genetics : EJHG|March 14, 2000
Clinical and molecular advances in autosomal dominant cerebellar ataxias: from genotype to phenotype and physiopathologyG Stevanin, A Dürr, A Brice
Revue Neurologique|May 27, 2015
Clinical and genetic heterogeneity in hereditary spastic paraplegias: from SPG1 to SPG72 and still countingS Klebe, G Stevanin, C Depienne
Revue Neurologique|April 29, 2017
Hereditary spastic paraplegia: More than an upper motor neuron diseaseL Parodi, S Fenu, G Stevanin, et al.
Neurology|October 16, 1999
Clinical and MRI findings in spinocerebellar ataxia type 5G Stevanin, A Herman, A Brice, et al.
Neurology|September 15, 2004
Mutations in the FGF14 gene are not a major cause of spinocerebellar ataxia in CaucasiansG Stevanin, A Durr, C Dussert, et al.
Revue Neurologique|May 7, 2011
Autosomal dominant cerebellar ataxiasC Marelli, C Cazeneuve, A Brice, et al.
Neurology|November 1, 1993
Familial essential tremor and idiopathic torsion dystonia are different genetic entitiesA Dürr, G Stevanin, C P Jedynak, et al.
Acta Neurologica Scandinavica. Supplementum|June 18, 2008
SPG11--the most common type of recessive spastic paraplegia in Norway?A K Erichsen, G Stevanin, P Denora, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1997
Saccade velocity in idiopathic and autosomal dominant cerebellar ataxiaK Bürk, M Fetter, M Skalej, et al.
American Journal of Human Genetics|May 20, 1999
Molecular and clinical study of 18 families with ADCA type II: evidence for genetic heterogeneity and de novo mutationP Giunti, G Stevanin, P F Worth, et al.
Pageof 9