DiDonato S - Search Results

1

Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy.

Mariotti C, Tiranti V, Carrara F, Dallapiccola B, DiDonato S, Zeviani M. Mariotti C, et al. Among authors: didonato s. J Clin Invest. 1994 Mar;93(3):1102-7. doi: 10.1172/JCI117061. J Clin Invest. 1994. PMID: 8132749 Free PMC article.

2

Mitochondrial disorders.

Zeviani M, Di Donato S. Zeviani M, et al. Brain. 2004 Oct;127(Pt 10):2153-72. doi: 10.1093/brain/awh259. Epub 2004 Sep 9. Brain. 2004. PMID: 15358637 Review.

3

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: didonato s. Lancet. 1991 Jul 20;338(8760):143-7. doi: 10.1016/0140-6736(91)90136-d. Lancet. 1991. PMID: 1677065

4

Neurological disorders due to mutations of the mitochondrial genome.

Zeviani M, DiDonato S. Zeviani M, et al. Among authors: didonato s. Neuromuscul Disord. 1991;1(3):165-72. doi: 10.1016/0960-8966(91)90020-s. Neuromuscul Disord. 1991. PMID: 1822790 Review.

5

Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA.

Mariotti C, Savarese N, Suomalainen A, Rimoldi M, Comi G, Prelle A, Antozzi C, Servidei S, Jarre L, DiDonato S, Zeviani M. Mariotti C, et al. Among authors: didonato s. J Neurol. 1995 May;242(5):304-12. doi: 10.1007/BF00878873. J Neurol. 1995. PMID: 7643139

6

A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene.

Zeviani M, Muntoni F, Savarese N, Serra G, Tiranti V, Carrara F, Mariotti C, DiDonato S. Zeviani M, et al. Among authors: didonato s. Eur J Hum Genet. 1993;1(1):80-7. doi: 10.1159/000472390. Eur J Hum Genet. 1993. PMID: 8069654

7

Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic study.

Mariotti C, Uziel G, Carrara F, Mora M, Prelle A, Tiranti V, DiDonato S, Zeviani M. Mariotti C, et al. Among authors: didonato s. J Neurol. 1995 Sep;242(9):547-56. doi: 10.1007/BF00868806. J Neurol. 1995. PMID: 8551315

8

A full-length cDNA encoding a mitochondrial DNA-specific single-stranded DNA binding protein from Xenopus laevis.

Tiranti V, Barat-Gueride B, Bijl J, DiDonato S, Zeviani M. Tiranti V, et al. Among authors: didonato s. Nucleic Acids Res. 1991 Aug 11;19(15):4291. doi: 10.1093/nar/19.15.4291. Nucleic Acids Res. 1991. PMID: 1870981 Free PMC article. No abstract available.

9

Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).

Zeviani M, Amati P, Bresolin N, Antozzi C, Piccolo G, Toscano A, DiDonato S. Zeviani M, et al. Among authors: didonato s. Am J Hum Genet. 1991 Feb;48(2):203-11. Am J Hum Genet. 1991. PMID: 1899320 Free PMC article.

10

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: didonato s. Am J Hum Genet. 1990 Dec;47(6):904-14. Am J Hum Genet. 1990. PMID: 1978558 Free PMC article.

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