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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.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 10, 2000
Genetic analysis of immunomodulating factors in sporadic Parkinson's diseaseR Krüger, C Hardt, F Tschentscher, et al.
Annals of Neurology|March 1, 1997
Genetic predisposition to multiple sclerosis as revealed by immunoprintingC Epplen, S Jäckel, E J Santos, et al.
Genes and Immunity|April 24, 2009
Association of UCP2 -866 G/A polymorphism with chronic inflammatory diseasesX Yu, S Wieczorek, A Franke, et al.
Gut|June 16, 2005
Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's diseaseH-P Török, J Glas, L Tonenchi, et al.
Neurogenetics|May 1, 1997
SCA2 trinucleotide expansion in German SCA patientsO Riess, F A Laccone, S Gispert, et al.
Journal of the American Society of Nephrology : JASN|September 7, 1999
Worldwide ethnic distribution of the G protein beta3 subunit 825T allele and its association with obesity in Caucasian, Chinese, and Black African individualsW Siffert, P Forster, K H Jöckel, et al.
Neurology|April 13, 2005
Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severityR H S R Roxburgh, S R Seaman, T Masterman, et al.
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