Taroni F - Search Results

1

Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations.

Gellera C, Castellotti B, Riggio MC, Silani V, Morandi L, Testa D, Casali C, Taroni F, Di Donato S, Zeviani M, Mariotti C. Gellera C, et al. Among authors: taroni f. Neuromuscul Disord. 2001 May;11(4):404-10. doi: 10.1016/s0960-8966(00)00215-7. Neuromuscul Disord. 2001. PMID: 11369193

2

Localization of the human gene for carnitine palmitoyltransferase to 1p13-p11 by nonradioactive in situ hybridization.

Minoletti F, Colombo I, Martin AL, Di Donato S, Taroni F, Finocchiaro G, Pandolfo M. Minoletti F, et al. Among authors: taroni f. Genomics. 1992 Aug;13(4):1372-4. doi: 10.1016/0888-7543(92)90076-5. Genomics. 1992. Retraction in: Genomics. 1994 Nov 1;24(1):198. PMID: 1339389 Retracted. No abstract available.

3

Biochemical and molecular studies of carnitine palmitoyltransferase II deficiency with hepatocardiomyopathic presentation.

Taroni F, Verderio E, Garavaglia B, Fiorucci S, Finocchiaro G, Uziel G, DiDonato S. Taroni F, et al. Prog Clin Biol Res. 1992;375:521-31. Prog Clin Biol Res. 1992. PMID: 1438396 No abstract available.

4

Molecular characterization of inherited carnitine palmitoyltransferase II deficiency.

Taroni F, Verderio E, Fiorucci S, Cavadini P, Finocchiaro G, Uziel G, Lamantea E, Gellera C, DiDonato S. Taroni F, et al. Proc Natl Acad Sci U S A. 1992 Sep 15;89(18):8429-33. doi: 10.1073/pnas.89.18.8429. Proc Natl Acad Sci U S A. 1992. PMID: 1528846 Free PMC article.

5

cDNA cloning, sequence analysis, and chromosomal localization of human carnitine palmitoyltransferase.

Finocchiaro G, Taroni F, Rocchi M, Liras Martin A, Colombo I, Tarelli GT, DiDonato S. Finocchiaro G, et al. Among authors: taroni f. Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10981. doi: 10.1073/pnas.88.23.10981. Proc Natl Acad Sci U S A. 1991. PMID: 1961767 Free PMC article. No abstract available.

6

cDNA cloning, sequence analysis, and chromosomal localization of the gene for human carnitine palmitoyltransferase.

Finocchiaro G, Taroni F, Rocchi M, Martin AL, Colombo I, Tarelli GT, DiDonato S. Finocchiaro G, et al. Among authors: taroni f. Proc Natl Acad Sci U S A. 1991 Jan 15;88(2):661-5. doi: 10.1073/pnas.88.2.661. Proc Natl Acad Sci U S A. 1991. PMID: 1988962 Free PMC article.

7

Purification and properties of cytosolic malic enzyme from human skeletal muscle.

Taroni F, Di Donato S. Taroni F, et al. Int J Biochem. 1988;20(8):857-66. doi: 10.1016/0020-711x(88)90075-4. Int J Biochem. 1988. PMID: 3169368

8

Glutamate dehydrogenase in OPCA.

Finocchiaro G, Taroni F, Di Donato S. Finocchiaro G, et al. Among authors: taroni f. Neurology. 1987 Oct;37(10):1687. doi: 10.1212/wnl.37.10.1687-b. Neurology. 1987. PMID: 3477705 No abstract available.

9

Evidence for two distinct mitochondrial malic enzymes in human skeletal muscle: purification and properties of the NAD(P)+-dependent enzyme.

Taroni F, Gellera C, Di Donato S. Taroni F, et al. Biochim Biophys Acta. 1987 Dec 18;916(3):446-54. doi: 10.1016/0167-4838(87)90191-9. Biochim Biophys Acta. 1987. PMID: 3689803

10

Glutamate dehydrogenase in olivopontocerebellar atrophies: leukocytes, fibroblasts, and muscle mitochondria.

Finocchiaro G, Taroni F, Di Donato S. Finocchiaro G, et al. Among authors: taroni f. Neurology. 1986 Apr;36(4):550-3. doi: 10.1212/wnl.36.4.550. Neurology. 1986. PMID: 3960332

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