Items where Author is "Finocchiaro, G"

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.

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., 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.