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Journal of Neural Transmission (Vienna, Austria : 1996)
|
May 5, 1999
Analysis of the parkin deletion in sporadic and familial Parkinson's disease. Short communication
R 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 disease
A S Glass, D P Huynh, Th Franck, et al.
Nature Genetics
|
February 14, 1998
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
R Krüger, W Kuhn, T Müller, et al.
Neurology
|
April 14, 2004
Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease
R Hering, S Petrovic, E-M Mietz, et al.
Neuroreport
|
August 16, 2000
Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease
R Krüger, A M Menezes-Saecker, L Schöls, et al.
The British Journal of Dermatology
|
March 15, 2016
Parkinson disease and multiple sclerosis are not associated with autoantibodies against structural proteins of the dermal-epidermal junction
A Recke, A Oei, F Hübner, et al.
Neuroreport
|
August 3, 2000
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients
P Wintermeyer, R Krüger, W Kuhn, et al.
Neurology
|
May 29, 2001
Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers
R Krüger, W Kuhn, K L Leenders, et al.
Annals of Neurology
|
May 13, 1999
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype
R Krüger, A M Vieira-Saecker, W Kuhn, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
November 10, 2000
Genetic analysis of immunomodulating factors in sporadic Parkinson's disease
R Krüger, C Hardt, F Tschentscher, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 54) with videos related to
Sort By:
Page
of 6
Journal of Neural Transmission (Vienna, Austria : 1996)
|
May 5, 1999
Analysis of the parkin deletion in sporadic and familial Parkinson's disease. Short communication
R 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 disease
A S Glass, D P Huynh, Th Franck, et al.
Nature Genetics
|
February 14, 1998
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease
R Krüger, W Kuhn, T Müller, et al.
Neurology
|
April 14, 2004
Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease
R Hering, S Petrovic, E-M Mietz, et al.
Neuroreport
|
August 16, 2000
Genetic analysis of the alpha2-macroglobulin gene in early- and late-onset Parkinson's disease
R Krüger, A M Menezes-Saecker, L Schöls, et al.
The British Journal of Dermatology
|
March 15, 2016
Parkinson disease and multiple sclerosis are not associated with autoantibodies against structural proteins of the dermal-epidermal junction
A Recke, A Oei, F Hübner, et al.
Neuroreport
|
August 3, 2000
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients
P Wintermeyer, R Krüger, W Kuhn, et al.
Neurology
|
May 29, 2001
Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers
R Krüger, W Kuhn, K L Leenders, et al.
Annals of Neurology
|
May 13, 1999
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype
R Krüger, A M Vieira-Saecker, W Kuhn, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
November 10, 2000
Genetic analysis of immunomodulating factors in sporadic Parkinson's disease
R Krüger, C Hardt, F Tschentscher, et al.
Page
of 6