Servidei S - Search Results

1

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: servidei s. Neurology. 2013 May 28;80(22):2049-54. doi: 10.1212/WNL.0b013e318294b44c. Epub 2013 May 1. Neurology. 2013. PMID: 23635963

2

Giant axonal neuropathy: report on a case with focal fiber loss.

Sabatelli M, Bertini E, Servidei S, Fernandez E, Magi S, Tonali P. Sabatelli M, et al. Among authors: servidei s. Acta Neuropathol. 1992;83(5):543-6. doi: 10.1007/BF00310034. Acta Neuropathol. 1992. PMID: 1621511

3

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

4

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

5

Metabolic causes of myoglobinuria.

Tonin P, Lewis P, Servidei S, DiMauro S. Tonin P, et al. Among authors: servidei s. Ann Neurol. 1990 Feb;27(2):181-5. doi: 10.1002/ana.410270214. Ann Neurol. 1990. PMID: 2156480

6

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: servidei s. Ann Neurol. 1990 Jul;28(1):94-7. doi: 10.1002/ana.410280118. Ann Neurol. 1990. PMID: 2375642

7

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: servidei s. Nature. 1989 May 25;339(6222):309-11. doi: 10.1038/339309a0. Nature. 1989. PMID: 2725645

8

Cytochrome c oxidase deficiency in Leigh syndrome.

DiMauro S, Servidei S, Zeviani M, DiRocco M, DeVivo DC, DiDonato S, Uziel G, Berry K, Hoganson G, Johnsen SD, et al. DiMauro S, et al. Among authors: servidei s. Ann Neurol. 1987 Oct;22(4):498-506. doi: 10.1002/ana.410220409. Ann Neurol. 1987. PMID: 2829705

9

Mitochondrial encephalomyopathy and partial cytochrome c oxidase deficiency.

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

10

Benign reversible muscle cytochrome c oxidase deficiency: a second case.

Zeviani M, Peterson P, Servidei S, Bonilla E, DiMauro S. Zeviani M, et al. Among authors: servidei s. Neurology. 1987 Jan;37(1):64-7. doi: 10.1212/wnl.37.1.64. Neurology. 1987. PMID: 3025776

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