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Fortschritte Der Neurologie-Psychiatrie|April 12, 2011
[Neurological manifestations of AGel amyloidosis (Meretoja's syndrome) in a German family]J Bürmann, K Fassbender, W Henn, et al.Journal of Materials Science. Materials in Medicine|September 7, 2004
A new composite made of polyurethane and glass ceramic in a loaded implant model: a biomechanical and histological analysisA Ignatius, K Unterricker, K Wenger, et al.The Journal of Clinical Investigation|February 11, 1992
Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met)H G Klein, P Lohse, P H Pritchard, et al.Neurology|November 26, 2008
Multiple sclerosis and the TNFRSF1A R92Q mutation: clinical characteristics of 21 casesT Kümpfel, L-A Hoffmann, H Pellkofer, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|October 30, 2014
Successful treatment of PASH syndrome with infliximab, cyclosporine and dapsoneJ Staub, N Pfannschmidt, R Strohal, et al.Journal of Lipid Research|November 11, 1992
Familial apolipoprotein E deficiency and type III hyperlipoproteinemia due to a premature stop codon in the apolipoprotein E geneP Lohse, H B Brewer, M S Meng, et al.Therapeutic Apheresis : Official Journal of the International Society for Apheresis and the Japanese Society for Apheresis|November 29, 2001
Consistent lowering of clotting factors for the treatment of acute cardiovascular syndromes and hypercoagulability: a different pathophysiological approachB R Jaeger, P Goehring, J Schirmer, et al.European Journal of Pediatrics|August 21, 2012
Familial Mediterranean fever in Germany: epidemiological, clinical, and genetic characteristics of a pediatric populationE Lainka, M Bielak, P Lohse, et al.American Journal of Reproductive Immunology (New York, N.Y. : 1989)|August 17, 2001
Thrombophilic gene mutations and recurrent spontaneous abortion: prothrombin mutation increases the risk in the first trimesterR Pihusch, T Buchholz, P Lohse, et al.Annals of the Rheumatic Diseases|January 9, 2008
Clinical and functional characterisation of a novel TNFRSF1A c.605T>A/V173D cleavage site mutation associated with tumour necrosis factor receptor-associated periodic fever syndrome (TRAPS), cardiovascular complications and excellent response to etanercept treatmentS Stojanov, C Dejaco, P Lohse, et al.Pageof 10