Items where Author is "Taroni, F"

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VERDERIO, E., CAVADINI, P., MONTERMINI, L., WANG, H., LAMANTEA, E., FINOCCHIARO, G., DIDONATO, S., GELLERA, C. and TARONI, F., 1995. Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations. Human Molecular Genetics, 4, pp. 19-29.

MONTERMINI, L., WANG, H., VERDERIO, E., TARONI, F., DIDONATO, S. and FINOCCHIARO, G., 1994. Identification of 5' regulatory regions of the human carnitine palmitoyltransferase II gene. Biochimica et Biophysica Acta, 1219, pp. 237-240.

TARONI, F., VERDERIO, E., DWORZAK, F., WILLEMS, P.J., CAVADINI, P. and DIDONATO, S., 1993. Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients. Nature Genetics, 4, pp. 314-320.

VERDERIO, E., CAVADINI, P., DIDONATO, S. and TARONI, F., 1993. Two novel sequence polymorphisms of the human carnitine palmitoyltransferase II (CPT-1) gene. Human Molecular Genetics, 2 (3), p. 334.

TARONI, F., VERDERIO, E., GARAVAGLIA, B., FIORRUCCI, S., FINOCCHIARO, G., UZIEL, G. and DIDONATO, S., 1992. Biochemical and molecular studies of carnitine palmitoyltransferase deficiency with hepatocardiomyopathic presentation. In: P.M. COATES and K. TANAKA, eds., New developments in fatty acid oxidation. New York: Wiley-Liss, pp. 521-531.

TARONI, F., VERDERIO, E., FIORUCCI, S., CAVADINI, P., FINOCCHIARO, G., UZIEL, G., LAMANTEA, E., GELLERA, C. and DIDONATO, S., 1992. Molecular characterization of inherited carnitine palmitoyltransferase II deficiency. Proceedings of the National Academy of Sciences of the United States of America, 89, pp. 8429-8433.

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