Items where Author is "DiDonato, S"

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Number of items: 6.

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.

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., 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.

Chapter in book

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.

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