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T Gasser

Showing results (271-280 of 316) with videos related to

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Neurology|May 12, 2004
Autosomal dominant parkinsonism associated with variable synuclein and tau pathologyZ K Wszolek, R F Pfeiffer, Y Tsuboi, et al.
Nature|October 17, 1998
The ubiquitin pathway in Parkinson's diseaseE Leroy, R Boyer, G Auburger, et al.
Nature Genetics|August 31, 2001
Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndromeA Zimprich, M Grabowski, F Asmus, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|December 29, 2004
The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodiesA Hofer, D Berg, F Asmus, et al.
Journal of Medical Genetics|January 31, 2006
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populationsM Sharma, J C Mueller, A Zimprich, et al.
FEBS Letters|July 1, 2005
Parkin interacts with the proteasome subunit alpha4J C Dächsel, C B Lücking, S Deeg, et al.
Neurology|August 12, 2011
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defectY G Weber, C Kamm, A Suls, et al.
Human Molecular Genetics|May 16, 1998
Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)J R Vaughan, M J Farrer, Z K Wszolek, et al.
European Journal of Neurology|March 16, 2013
No association of GBA mutations and multiple system atrophyK Srulijes, A-K Hauser, I Guella, et al.
Neurobiology of Disease|January 8, 2010
Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystoniaM Walter, M Bonin, R Saunders Pullman, et al.
Pageof 32

Showing results (271-280 of 316) with videos related to

Sort By:
Pageof 32
Neurology|May 12, 2004
Autosomal dominant parkinsonism associated with variable synuclein and tau pathologyZ K Wszolek, R F Pfeiffer, Y Tsuboi, et al.
Nature|October 17, 1998
The ubiquitin pathway in Parkinson's diseaseE Leroy, R Boyer, G Auburger, et al.
Nature Genetics|August 31, 2001
Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndromeA Zimprich, M Grabowski, F Asmus, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|December 29, 2004
The role of alpha-synuclein gene multiplications in early-onset Parkinson's disease and dementia with Lewy bodiesA Hofer, D Berg, F Asmus, et al.
Journal of Medical Genetics|January 31, 2006
The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populationsM Sharma, J C Mueller, A Zimprich, et al.
FEBS Letters|July 1, 2005
Parkin interacts with the proteasome subunit alpha4J C Dächsel, C B Lücking, S Deeg, et al.
Neurology|August 12, 2011
Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defectY G Weber, C Kamm, A Suls, et al.
Human Molecular Genetics|May 16, 1998
Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)J R Vaughan, M J Farrer, Z K Wszolek, et al.
European Journal of Neurology|March 16, 2013
No association of GBA mutations and multiple system atrophyK Srulijes, A-K Hauser, I Guella, et al.
Neurobiology of Disease|January 8, 2010
Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystoniaM Walter, M Bonin, R Saunders Pullman, et al.
Pageof 32