Ruebsamen H - Search Results

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R116C mutation of cationic trypsinogen in a Turkish family with recurrent pancreatitis illustrates genetic microheterogeneity of hereditary pancreatitis.

Tautermann G, Ruebsamen H, Beck M, Dertinger S, Drexel H, Lohse P. Tautermann G, et al. Among authors: ruebsamen h. Digestion. 2001;64(4):226-32. doi: 10.1159/000048866. Digestion. 2001. PMID: 11842279

S680N substitution of the follicle-stimulating hormone receptor is a common polymorphism not associated with spontaneous human twinning.

Hasbargen U, Thaler CJ, Ruebsamen H, Fuchshuber S, Lohse P. Hasbargen U, et al. Among authors: ruebsamen h. Eur J Med Res. 2001 Jul 30;6(7):315-6. Eur J Med Res. 2001. PMID: 11485893

Effects of the common 677C>T mutation of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene on ovarian responsiveness to recombinant follicle-stimulating hormone.

Thaler CJ, Budiman H, Ruebsamen H, Nagel D, Lohse P. Thaler CJ, et al. Among authors: ruebsamen h. Am J Reprod Immunol. 2006 Apr;55(4):251-8. doi: 10.1111/j.1600-0897.2005.00357.x. Am J Reprod Immunol. 2006. PMID: 16533336

Microsatellite instability, loss of heterozygosity, and loss of hMLH1 and hMSH2 protein expression in endometrial carcinoma.

Peiró G, Diebold J, Lohse P, Ruebsamen H, Lohse P, Baretton GB, Löhrs U. Peiró G, et al. Among authors: ruebsamen h. Hum Pathol. 2002 Mar;33(3):347-54. doi: 10.1053/hupa.2002.32220. Hum Pathol. 2002. PMID: 11979377

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