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European Journal of Biochemistry|March 1, 1995
Murine liver homogentisate 1,2-dioxygenase. Purification to homogeneity and novel biochemical propertiesS R Schmidt, C R Müller, W Kress
Neuroscience Letters|July 9, 1998
Serum levels of macrophage-derived protein MRP-8/14 are elevated in active multiple sclerosisT Bogumil, P Rieckmann, B Kubuschok, et al.
Annals of the New York Academy of Sciences|May 4, 1992
Lymphokine production by B cells from normal and HIV-infected individualsJ H Kehrl, P Rieckmann, E Kozlow, et al.
Research in Experimental Medicine. Zeitschrift Fur Die Gesamte Experimentelle Medizin Einschliesslich Experimenteller Chirurgie|January 1, 1995
Semi-quantitative analysis of cytokine gene expression in blood and cerebrospinal fluid cells by reverse transcriptase polymerase chain reactionP Rieckmann, M Albrecht, H Ehrenreich, et al.
Neurology|November 6, 2009
Impact of multiple sclerosis relapses on progression diminishes with timeH Tremlett, M Yousefi, V Devonshire, et al.
Tissue Antigens|October 10, 2006
Analysis of the C/T(-1) single nucleotide polymorphism in the CD40 gene in multiple sclerosisD Buck, A Kroner, P Rieckmann, et al.
The Journal of Experimental Medicine|January 1, 1991
Activated B lymphocytes from human immunodeficiency virus-infected individuals induce virus expression in infected T cells and a promonocytic cell line, U1P Rieckmann, G Poli, J H Kehrl, et al.
Conference Proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference|February 3, 2007
Biomechanics of femoral deformity in osteogenesis imperfecta (OI): a quantitative approach to rehabilitationZ Fan, P Smith, K Reiners, et al.
Cytogenetics and Cell Genetics|August 18, 1999
The novel contiguous gene syndrome of myotubular myopathy (MTM1), male hypogenitalism and deletion in Xq28:report of the first familial caseO Bartsch, W Kress, A Wagner, et al.
Clinical Genetics|September 14, 2007
Endocardial cushion defect in a patient with Crouzon syndrome carrying a mutation in the fibroblast growth factor receptor (FGFR)-2 geneC Schulz, W Kress, A Schömig, et al.
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