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Wiener Klinische Wochenschrift. Supplementum|January 1, 1990
[Determination of fructosamine in chronic kidney diseases (dialysis-dependent patients)]E Peheim, C Descoeudres, P Diem, et al.
British Journal of Clinical Pharmacology|December 1, 1979
The effect of enzyme induction on diazepam metabolism in manE E Ohnhaus, B K Park, J P Colombo, et al.
Acta Haematologica|January 1, 1986
Reactivity of monoclonal antibodies LAU-A1 and anti-Y 29/55 in T and B cell malignancies of children: correlation with immunological markers and clinical dataA Hirt, S Carrel, H K Forster, et al.
Schweizerische Medizinische Wochenschrift|October 10, 1981
[Treatment of severe aplastic anemia]A Gratwohl, B Osterwalder, C Nissen, et al.
European Journal of Pediatrics|July 1, 1985
Homozygous hypobetalipoproteinaemia and phenylketonuriaJ U Leititis, M Stahl, W Tackmann, et al.
Helvetica Paediatrica Acta|January 1, 1979
Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathologyE R Baumgartner, H Wick, R Maurer, et al.
Arzneimittel-Forschung|February 5, 1998
Organogermanium compounds as inhibitors of the activity of direct acting mutagens in Salmonella typhimuriumO Schimmer, H Eschelbach, D K Breitinger, et al.
Human Mutation|January 1, 1996
Ornithine transcarbamylase deficiency: characterization of gene mutations and polymorphismsE O Oppliger Leibundgut, B Wermuth, J P Colombo, et al.
Enzyme|January 1, 1991
Direct and indirect mutation analyses in patients with ornithine transcarbamylase deficiencyS Liechti-Gallati, C Dionisi, C Bachmann, et al.
Pediatric Research|September 1, 1987
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome: low creatine excretion and effect of citrulline, arginine, or ornithine supplementC Dionisi Vici, C Bachmann, M Gambarara, et al.
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