Items where Author is "Cavadini, P"

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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.

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