Gellera C - Search Results

1

Normalization of short-chain acylcoenzyme A dehydrogenase after riboflavin treatment in a girl with multiple acylcoenzyme A dehydrogenase-deficient myopathy.

DiDonato S, Gellera C, Peluchetti D, Uziel G, Antonelli A, Lus G, Rimoldi M. DiDonato S, et al. Among authors: gellera c. Ann Neurol. 1989 May;25(5):479-84. doi: 10.1002/ana.410250510. Ann Neurol. 1989. PMID: 2774489

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

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

Zeviani M, Gellera C, Antozzi C, Rimoldi M, Morandi L, Villani F, Tiranti V, DiDonato S. Zeviani M, et al. Among authors: gellera c. Lancet. 1991 Jul 20;338(8760):143-7. doi: 10.1016/0140-6736(91)90136-d. Lancet. 1991. PMID: 1677065

5

[Metabolic myopathies].

Finocchiaro G, Zeviani M, Garavaglia B, Gellera C, Bertagnolio B, Rimoldi M, Di Donato S. Finocchiaro G, et al. Among authors: gellera c. Minerva Pediatr. 1991 Mar;43(3):81-9. Minerva Pediatr. 1991. PMID: 1870530 Italian. No abstract available.

6

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.

7

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

8

Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymes.

Gellera C, Uziel G, Rimoldi M, Zeviani M, Laverda A, Carrara F, DiDonato S. Gellera C, et al. Neurology. 1990 Mar;40(3 Pt 1):495-9. doi: 10.1212/wnl.40.3_part_1.495. Neurology. 1990. PMID: 2314594

9

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.

10

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

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