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Pediatric Research|July 1, 1975
Acute neonatal nonketotic hyperglycinemia: normal propionate and methylmalonate metabolismE R Baumgartner, C Bachmann, T Brechbühler, et al.Schweizerische Medizinische Wochenschrift. Supplementum|January 1, 1981
[Distribution of plasma cholesterol in 4 Swiss cities]H Micheli, H B Stähelin, C Bachmann, 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.Human Genetics|February 1, 1995
Ornithine transcarbamylase deficiency: new sites with increased probability of mutationE O Oppliger Leibundgut, S Liechti-Gallati, J P Colombo, et al.Zeitschrift Fur Kinderheilkunde|January 1, 1975
Unsuccessful trial of gene replacement in arginase deficiencyH G Terheggen, A Lowenthal, F Lavinha, et al.Padiatrie Und Padologie|January 1, 1991
[Macrocephaly and dystonic cerebral palsy in a child with type I glutaric aciduria]E Plöchl, E Christensen, J P Colombo, et al.Journal of Neurochemistry|August 1, 1994
Photoaffinity labeling of the cerebral sulfonylurea receptor using a novel radioiodinated azidoglibenclamide analogueM Schwanstecher, S Löser, F Chudziak, et al.Archives of Gynecology|January 1, 1985
Activities in the placenta and fetal membranes of enzymes involved in energy metabolismU Herrmann, P Degiampietro, E Metzger, et al.Metabolism: Clinical and Experimental|April 1, 1982
Reversal of diuretic-induced increases in serum low-density-lipoprotein cholesterol by the betablocker pindololH Schiffl, P Weidmann, R Mordasini, et al.Brain Research. Molecular Brain Research|July 17, 1999
L-arginine uptake, the citrulline-NO cycle and arginase II in the rat brain: an in situ hybridization studyO Braissant, T Gotoh, M Loup, et al.Pageof 25