Items where Author is "Taroni, F"

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Number of items: 6.

Journal article

Verderio, E ORCID: 0000-0001-9153-8997, 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 ORCID: 0000-0001-9153-8997, 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 ORCID: 0000-0001-9153-8997, Dworzak, F, Willems, PJ, 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 ORCID: 0000-0001-9153-8997, 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 ORCID: 0000-0001-9153-8997, 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 ORCID: 0000-0001-9153-8997, Garavaglia, B, Fiorrucci, S, Finocchiaro, G, Uziel, G and DiDonato, S, 1992. Biochemical and molecular studies of carnitine palmitoyltransferase deficiency with hepatocardiomyopathic presentation. In: Coates, PM and Tanaka, K, eds., New developments in fatty acid oxidation. New York: Wiley-Liss, pp. 521-531.

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