Items where Author is "Cavadini, P"

Journal article

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.

GELLERA, C., VERDERIO, E., FLORIDIA, G., FINOCCHIARO, G., MONTERMINI, L., CAVADINI, P., ZUFFARDI, O. and TASSE, C., 1994. Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32. Genomics, 24, pp. 195-197.

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., 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.