Zeviani M - Search Results

1

A novel nonsense mutation (Q352X) in the mitochondrial cytochrome b gene associated with a combined deficiency of complexes I and III.

Lamantea E, Carrara F, Mariotti C, Morandi L, Tiranti V, Zeviani M. Lamantea E, et al. Among authors: zeviani m. Neuromuscul Disord. 2002 Jan;12(1):49-52. doi: 10.1016/s0960-8966(01)00244-9. Neuromuscul Disord. 2002. PMID: 11731284

2

Defects of mitochondrial DNA.

Zeviani M, Antozzi C. Zeviani M, et al. Brain Pathol. 1992 Apr;2(2):121-32. doi: 10.1111/j.1750-3639.1992.tb00680.x. Brain Pathol. 1992. PMID: 1341953 Review.

3

Nucleus-driven mutations of human mitochondrial DNA.

Zeviani M. Zeviani M. J Inherit Metab Dis. 1992;15(4):456-71. doi: 10.1007/BF01799604. J Inherit Metab Dis. 1992. PMID: 1528006 Review.

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

5

Neurological disorders due to mutations of the mitochondrial genome.

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

6

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: zeviani m. 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.

7

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. Am J Hum Genet. 1991 Feb;48(2):203-11. Am J Hum Genet. 1991. PMID: 1899320 Free PMC article.

8

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

9

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: zeviani m. Neurology. 1991 Jul;41(7):1053-9. doi: 10.1212/wnl.41.7.1053. Neurology. 1991. PMID: 2067633

10

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. Among authors: zeviani m. Neurology. 1990 Mar;40(3 Pt 1):495-9. doi: 10.1212/wnl.40.3_part_1.495. Neurology. 1990. PMID: 2314594

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