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O Riess

Showing results (121-130 of 144) with videos related to

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Neuroreport|August 3, 2000
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patientsP Wintermeyer, R Krüger, W Kuhn, et al.
Neurology|September 26, 1997
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6T Sander, B Bockenkamp, T Hildmann, et al.
Brain : a Journal of Neurology|May 13, 1998
The natural history of degenerative ataxia: a retrospective study in 466 patientsT Klockgether, R Lüdtke, B Kramer, et al.
Human Molecular Genetics|August 1, 1997
SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel geneO Riess, L Schöls, H Bottger, et al.
American Journal of Medical Genetics|April 17, 1999
Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14T Sander, H Schulz, A M Vieira-Saeker, et al.
Annals of Neurology|May 13, 1999
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotypeR Krüger, A M Vieira-Saecker, W Kuhn, et al.
Neurology|May 29, 2001
Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriersR Krüger, W Kuhn, K L Leenders, et al.
Psychiatric Genetics|April 28, 2001
Exonic variants of the GABA(B) receptor gene and panic disorderP G Sand, C Godau, P Riederer, et al.
Acta Neurologica Scandinavica|November 24, 2011
Autosomal dominant Parkinson's disease in a large German pedigreeN Brüggemann, W Külper, J Hagenah, et al.
Neurobiology of Disease|July 3, 2007
Overexpression of human wildtype torsinA and human DeltaGAG torsinA in a transgenic mouse model causes phenotypic abnormalitiesK Grundmann, B Reischmann, G Vanhoutte, et al.
Pageof 15

Showing results (121-130 of 144) with videos related to

Sort By:
Pageof 15
Neuroreport|August 3, 2000
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patientsP Wintermeyer, R Krüger, W Kuhn, et al.
Neurology|September 26, 1997
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6T Sander, B Bockenkamp, T Hildmann, et al.
Brain : a Journal of Neurology|May 13, 1998
The natural history of degenerative ataxia: a retrospective study in 466 patientsT Klockgether, R Lüdtke, B Kramer, et al.
Human Molecular Genetics|August 1, 1997
SCA6 is caused by moderate CAG expansion in the alpha1A-voltage-dependent calcium channel geneO Riess, L Schöls, H Bottger, et al.
American Journal of Medical Genetics|April 17, 1999
Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14T Sander, H Schulz, A M Vieira-Saeker, et al.
Annals of Neurology|May 13, 1999
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotypeR Krüger, A M Vieira-Saecker, W Kuhn, et al.
Neurology|May 29, 2001
Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriersR Krüger, W Kuhn, K L Leenders, et al.
Psychiatric Genetics|April 28, 2001
Exonic variants of the GABA(B) receptor gene and panic disorderP G Sand, C Godau, P Riederer, et al.
Acta Neurologica Scandinavica|November 24, 2011
Autosomal dominant Parkinson's disease in a large German pedigreeN Brüggemann, W Külper, J Hagenah, et al.
Neurobiology of Disease|July 3, 2007
Overexpression of human wildtype torsinA and human DeltaGAG torsinA in a transgenic mouse model causes phenotypic abnormalitiesK Grundmann, B Reischmann, G Vanhoutte, et al.
Pageof 15