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O Riess

Showing results (101-110 of 144) with videos related to

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Journal of Neural Transmission (Vienna, Austria : 1996)|June 18, 2003
Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's diseaseT Schulte, S Böhringer, L Schöls, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 5, 1999
Analysis of the parkin deletion in sporadic and familial Parkinson's disease. Short communicationR Krüger, A M Vieira-Säcker, W Kuhn, et al.
Journal of Neural Transmission. Supplementum|September 10, 2004
Screening for mutations in synaptotagmin XI in Parkinson's diseaseA S Glass, D P Huynh, Th Franck, et al.
Clinical Genetics|August 31, 2012
Novel SLC9A6 mutations in two families with Christianson syndromeA Riess, E Rossier, R Krüger, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 10, 1999
Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD)T Klockgether, L Schöls, M Abele, et al.
Experimental Neurology|April 5, 2011
Metabolic and type 1 cannabinoid receptor imaging of a transgenic rat model in the early phase of Huntington diseaseC Casteels, C Vandeputte, J R Rangarajan, et al.
Human Molecular Genetics|August 1, 2000
CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)S Hayes, G Turecki, K Brisebois, et al.
Neurology|April 14, 2004
Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson diseaseR Hering, S Petrovic, E-M Mietz, et al.
Cytogenetic and Genome Research|February 7, 2008
Specific transcriptional changes in human fetuses with autosomal trisomiesO Altug-Teber, M Bonin, M Walter, et al.
American Journal of Medical Genetics|July 14, 1999
Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsyT Sander, C Peters, G Kämmer, et al.
Pageof 15

Showing results (101-110 of 144) with videos related to

Sort By:
Pageof 15
Journal of Neural Transmission (Vienna, Austria : 1996)|June 18, 2003
Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's diseaseT Schulte, S Böhringer, L Schöls, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|May 5, 1999
Analysis of the parkin deletion in sporadic and familial Parkinson's disease. Short communicationR Krüger, A M Vieira-Säcker, W Kuhn, et al.
Journal of Neural Transmission. Supplementum|September 10, 2004
Screening for mutations in synaptotagmin XI in Parkinson's diseaseA S Glass, D P Huynh, Th Franck, et al.
Clinical Genetics|August 31, 2012
Novel SLC9A6 mutations in two families with Christianson syndromeA Riess, E Rossier, R Krüger, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 10, 1999
Age related axonal neuropathy in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD)T Klockgether, L Schöls, M Abele, et al.
Experimental Neurology|April 5, 2011
Metabolic and type 1 cannabinoid receptor imaging of a transgenic rat model in the early phase of Huntington diseaseC Casteels, C Vandeputte, J R Rangarajan, et al.
Human Molecular Genetics|August 1, 2000
CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)S Hayes, G Turecki, K Brisebois, et al.
Neurology|April 14, 2004
Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson diseaseR Hering, S Petrovic, E-M Mietz, et al.
Cytogenetic and Genome Research|February 7, 2008
Specific transcriptional changes in human fetuses with autosomal trisomiesO Altug-Teber, M Bonin, M Walter, et al.
American Journal of Medical Genetics|July 14, 1999
Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsyT Sander, C Peters, G Kämmer, et al.
Pageof 15