Zeviani M - Search Results

1

A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNA (Lys) gene associated with myoclonus epilepsy with ragged-red fibers.

Arenas J, Campos Y, Bornstein B, Ribacoba R, Martín MA, Rubio JC, Santorelli FM, Zeviani M, DiMauro S, Garesse R. Arenas J, et al. Among authors: zeviani m. Neurology. 1999 Jan 15;52(2):377-82. doi: 10.1212/wnl.52.2.377. Neurology. 1999. PMID: 9932960

2

Deletions of mitochondrial DNA in Kearns-Sayre syndrome.

Zeviani M, Moraes CT, DiMauro S, Nakase H, Bonilla E, Schon EA, Rowland LP. Zeviani M, et al. Neurology. 1988 Sep;38(9):1339-46. doi: 10.1212/wnl.38.9.1339. Neurology. 1988. PMID: 3412580

3

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

4

Mitochondrial myopathies.

DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo DC. DiMauro S, et al. Among authors: zeviani m. Ann Neurol. 1985 Jun;17(6):521-38. doi: 10.1002/ana.410170602. Ann Neurol. 1985. PMID: 3927817 Review.

5

The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathy.

Bruno C, Kirby DM, Koga Y, Garavaglia B, Duran G, Santorelli FM, Shield LK, Xia W, Shanske S, Goldstein JD, Iwanaga R, Akita Y, Carrara F, Davis A, Zeviani M, Thorburn DR, DiMauro S. Bruno C, et al. Among authors: zeviani m. J Pediatr. 1999 Aug;135(2 Pt 1):197-202. doi: 10.1016/s0022-3476(99)70022-3. J Pediatr. 1999. PMID: 10431114 Free article.

6

Mitochondrial encephalomyopathy and partial cytochrome c oxidase deficiency.

Servidei S, Lazaro RP, Bonilla E, Barron KD, Zeviani M, DiMauro S. Servidei S, et al. Among authors: zeviani m. Neurology. 1987 Jan;37(1):58-63. doi: 10.1212/wnl.37.1.58. Neurology. 1987. PMID: 3025775

7

The V368i mutation in Twinkle does not segregate with AdPEO.

Arenas J, Briem E, Dahl H, Hutchison W, Lewis S, Martin MA, Spelbrink H, Tiranti V, Jacobs H, Zeviani M. Arenas J, et al. Among authors: zeviani m. Ann Neurol. 2003 Feb;53(2):278. doi: 10.1002/ana.10430. Ann Neurol. 2003. PMID: 12557300 No abstract available.

8

Hepatocerebral form of mitochondrial DNA depletion syndrome: novel MPV17 mutations.

Spinazzola A, Santer R, Akman OH, Tsiakas K, Schaefer H, Ding X, Karadimas CL, Shanske S, Ganesh J, Di Mauro S, Zeviani M. Spinazzola A, et al. Among authors: zeviani m. Arch Neurol. 2008 Aug;65(8):1108-13. doi: 10.1001/archneur.65.8.1108. Arch Neurol. 2008. PMID: 18695062

9

Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation.

Mancuso M, Orsucci D, Angelini C, Bertini E, Carelli V, Comi GP, Minetti C, Moggio M, Mongini T, Servidei S, Tonin P, Toscano A, Uziel G, Bruno C, Caldarazzo Ienco E, Filosto M, Lamperti C, Martinelli D, Moroni I, Musumeci O, Pegoraro E, Ronchi D, Santorelli FM, Sauchelli D, Scarpelli M, Sciacco M, Spinazzi M, Valentino ML, Vercelli L, Zeviani M, Siciliano G. Mancuso M, et al. Among authors: zeviani m. Neurology. 2013 May 28;80(22):2049-54. doi: 10.1212/WNL.0b013e318294b44c. Epub 2013 May 1. Neurology. 2013. PMID: 23635963

10

Mitochondrial diseases.

Zeviani M, Bonilla E, DeVivo DC, DiMauro S. Zeviani M, et al. Neurol Clin. 1989 Feb;7(1):123-56. Neurol Clin. 1989. PMID: 2646519 Review.

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