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Neurology
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September 18, 2007
alpha-Synuclein and Parkinson disease susceptibility
S Winkler, J Hagenah, S Lincoln, et al.
Nuklearmedizin. Nuclear Medicine
|
March 19, 2004
[Multicenter study of radiosynoviorthesis. Clinical outcome in osteoarthritis and other disorders with concomitant synovitis in comparison with rheumatoid arthritis]
H Rau, K Lohmann, C Franke, et al.
European Journal of Biochemistry
|
April 2, 1999
Characterization of the cardiac holotroponin complex reconstituted from native cardiac troponin T and recombinant I and C
S Reiffert, R Maytum, M Geeves, et al.
Circulation Research
|
June 13, 2000
Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein
C Redwood, K Lohmann, W Bing, et al.
Journal of Clinical Pharmacy and Therapeutics
|
February 7, 2015
More than just crushing: a prospective pre-post intervention study to reduce drug preparation errors in patients with feeding tubes
K Lohmann, D Gartner, R Kurze, et al.
Neurology
|
April 8, 2009
Etiology of musician's dystonia: familial or environmental?
A Schmidt, H-C Jabusch, E Altenmüller, et al.
Neurology
|
April 22, 2009
The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?
N Brüggemann, N Kock, K Lohmann, et al.
Neurology
|
November 23, 2007
Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
K Lohmann-Hedrich, A Neumann, A Kleensang, et al.
Neurology
|
November 29, 2008
Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype
B F L van Nuenen, M M Weiss, B R Bloem, et al.
European Journal of Neurology
|
July 21, 2012
Glucocerebrosidase mutations in a Serbian Parkinson's disease population
K R Kumar, A Ramirez, A Göbel, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 44) with videos related to
Sort By:
Page
of 5
Neurology
|
September 18, 2007
alpha-Synuclein and Parkinson disease susceptibility
S Winkler, J Hagenah, S Lincoln, et al.
Nuklearmedizin. Nuclear Medicine
|
March 19, 2004
[Multicenter study of radiosynoviorthesis. Clinical outcome in osteoarthritis and other disorders with concomitant synovitis in comparison with rheumatoid arthritis]
H Rau, K Lohmann, C Franke, et al.
European Journal of Biochemistry
|
April 2, 1999
Characterization of the cardiac holotroponin complex reconstituted from native cardiac troponin T and recombinant I and C
S Reiffert, R Maytum, M Geeves, et al.
Circulation Research
|
June 13, 2000
Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein
C Redwood, K Lohmann, W Bing, et al.
Journal of Clinical Pharmacy and Therapeutics
|
February 7, 2015
More than just crushing: a prospective pre-post intervention study to reduce drug preparation errors in patients with feeding tubes
K Lohmann, D Gartner, R Kurze, et al.
Neurology
|
April 8, 2009
Etiology of musician's dystonia: familial or environmental?
A Schmidt, H-C Jabusch, E Altenmüller, et al.
Neurology
|
April 22, 2009
The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?
N Brüggemann, N Kock, K Lohmann, et al.
Neurology
|
November 23, 2007
Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
K Lohmann-Hedrich, A Neumann, A Kleensang, et al.
Neurology
|
November 29, 2008
Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype
B F L van Nuenen, M M Weiss, B R Bloem, et al.
European Journal of Neurology
|
July 21, 2012
Glucocerebrosidase mutations in a Serbian Parkinson's disease population
K R Kumar, A Ramirez, A Göbel, et al.
Page
of 5