Gellera C - Search Results

1

Errors in Huntington disease diagnostic test caused by trinucleotide deletion in the IT15 gene.

Gellera C, Meoni C, Castellotti B, Zappacosta B, Girotti F, Taroni F, DiDonato S. Gellera C, et al. Am J Hum Genet. 1996 Aug;59(2):475-7. Am J Hum Genet. 1996. PMID: 8755937 Free PMC article. No abstract available.

2

Molecular heterogeneity of beta-ETF deficiency in glutaric aciduria type II.

Colombo I, DiDonato S, Volta M, Gellera C, Garavaglia B, Montermini L, Yamaguchi S, Goodman SI, Frerman FE, Finocchiaro G. Colombo I, et al. Among authors: gellera c. Prog Clin Biol Res. 1992;375:561-6. Prog Clin Biol Res. 1992. PMID: 1438399 No abstract available.

3

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. Among authors: gellera c. 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.

4

Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease.

Zeviani M, Bresolin N, Gellera C, Bordoni A, Pannacci M, Amati P, Moggio M, Servidei S, Scarlato G, DiDonato S. Zeviani M, et al. Among authors: gellera c. Am J Hum Genet. 1990 Dec;47(6):904-14. Am J Hum Genet. 1990. PMID: 1978558 Free PMC article.

5

Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies.

Servidei S, Zeviani M, Manfredi G, Ricci E, Silvestri G, Bertini E, Gellera C, Di Mauro S, Di Donato S, Tonali P. Servidei S, et al. Among authors: gellera c. Neurology. 1991 Jul;41(7):1053-9. doi: 10.1212/wnl.41.7.1053. Neurology. 1991. PMID: 2067633

6

Short-chain and medium-chain acylCoA dehydrogenases are lowered in riboflavin-responsive lipid myopathies with multiple acylCoA dehydrogenase deficiency.

Di Donato S, Gellera C. Di Donato S, et al. Among authors: gellera c. Prog Clin Biol Res. 1990;321:325-32. Prog Clin Biol Res. 1990. PMID: 2326297 No abstract available.

7

Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies.

Zeviani M, Gellera C, Pannacci M, Uziel G, Prelle A, Servidei S, DiDonato S. Zeviani M, et al. Among authors: gellera c. Ann Neurol. 1990 Jul;28(1):94-7. doi: 10.1002/ana.410280118. Ann Neurol. 1990. PMID: 2375642

8

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.

Zeviani M, Servidei S, Gellera C, Bertini E, DiMauro S, DiDonato S. Zeviani M, et al. Among authors: gellera c. Nature. 1989 May 25;339(6222):309-11. doi: 10.1038/339309a0. Nature. 1989. PMID: 2725645

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. Among authors: gellera c. 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

Carnitine palmitoyltransferase II deficiency: structure of the gene and characterization of two novel disease-causing mutations.

Verderio E, Cavadini P, Montermini L, Wang H, Lamantea E, Finocchiaro G, DiDonato S, Gellera C, Taroni F. Verderio E, et al. Among authors: gellera c. Hum Mol Genet. 1995 Jan;4(1):19-29. doi: 10.1093/hmg/4.1.19. Hum Mol Genet. 1995. PMID: 7711730

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