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Scandinavian Journal of Rheumatology|November 10, 2012
Familial Mediterranean fever in Germany: clinical presentation and amyloidosis riskD Ebrahimi-Fakhari, S O Schönland, U Hegenbart, et al.Tissue Antigens|July 31, 2007
The role of the selenoprotein S (SELS) gene -105G>A promoter polymorphism in inflammatory bowel disease and regulation of SELS gene expression in intestinal inflammationJ Seiderer, J Dambacher, B Kühnlein, et al.European Journal of Medical Research|December 1, 2001
Sixteen rare sequence variants of the hMLH1 and hMSH2 genes found in a cohort of 254 suspected HNPCC (hereditary non-polyposis colorectal cancer) patients: mutations or polymorphisms?Y Müller-Koch, R Kopp, P Lohse, et al.Metabolism: Clinical and Experimental|November 1, 1993
Increased production of apolipoprotein A-I associated with elevated plasma levels of high-density lipoproteins, apolipoprotein A-I, and lipoprotein A-I in a patient with familial hyperalphalipoproteinemiaD J Rader, J R Schaefer, P Lohse, et al.Alimentary Pharmacology & Therapeutics|September 21, 2006
The +1059G/C polymorphism in the C-reactive protein (CRP) gene is associated with involvement of the terminal ileum and decreased serum CRP levels in patients with Crohn's diseaseD Thalmaier, J Dambacher, J Seiderer, et al.BMJ Case Reports|June 19, 2012
Respiratory distress syndrome due to a novel homozygous ABCA3 mutation in a term neonateHussain Parappil, Ahmad Al Baridi, Sajjad ur Rahman, et al.Gut|June 16, 2005
Hereditary non-polyposis colorectal cancer: clinical and molecular evidence for a new entity of hereditary colorectal cancerY Mueller-Koch, H Vogelsang, R Kopp, et al.Arthritis & Rheumatology (Hoboken, N.J.)|July 11, 2017
Clinical and Molecular Phenotypes of Low-Penetrance Variants of NLRP3: Diagnostic and Therapeutic ChallengesJ B Kuemmerle-Deschner, D Verma, T Endres, et al.Clinical Genetics|December 17, 2009
Respiratory disease in Niemann-Pick type C2 is caused by pulmonary alveolar proteinosisM Griese, F Brasch, V R Aldana, 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.Pageof 10