Publications

Found 1008 results
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1989
DiMauro S, Zeviani M, Moraes CT, Nakase H, Rizzuto R, Lombès A, Shanske S & Schon EA (1989) Mitochondrial encephalomyopathies. Prog Clin Biol Res 306, 117-28
Lombès A, Mendell JR, Nakase H, Barohn RJ, Bonilla E, Zeviani M, Yates AJ, Omerza J, Gales TL & Nakahara K (1989) Myoclonic epilepsy and ragged-red fibers with cytochrome oxidase deficiency: neuropathology, biochemistry, and molecular genetics. Ann Neurol 26, 20-33
1988
DiMauro S, Zeviani M, Servidei S, Prelle A, Miranda AF, Bonilla E & Schon EA (1988) Biochemical and molecular aspects of cytochrome C oxidase deficiency. Adv Neurol 48, 93-105
Schon EA, Bonilla E, Lombès A, Moraes CT, Nakase H, Rizzuto R, Zeviani M & DiMauro S (1988) Clinical and biochemical studies on cytochrome oxidase deficiencies. Ann N Y Acad Sci 550, 348-59
Zeviani M, Darras BT, Rizzuto R, Salviati G, Betto R, Bonilla E, Miranda AF, Du J, Samitt C & Dickson G (1988) Cloning and expression of human nebulin cDNAs and assignment of the gene to chromosome 2q31-q32. Genomics 2, 249-56
Zeviani M, Moraes CT, DiMauro S, Nakase H, Bonilla E, Schon EA & Rowland LP (1988) Deletions of mitochondrial DNA in Kearns-Sayre syndrome. Neurology 38, 1339-46
Bonilla E, Miranda AF, Prelle A, Salviati G, Betto R, Zeviani M, Schon EA, DiMauro S & Rowland LP (1988) Immunocytochemical study of nebulin in Duchenne muscular dystrophy. Neurology 38, 1600-3
Servidei S, Shanske S, Zeviani M, Lebo R, Fletterick R & DiMauro S (1988) McArdle's disease: biochemical and molecular genetic studies. Ann Neurol 24, 774-81
Montagna P, Gallassi R, Medori R, Govoni E, Zeviani M, Di Mauro S, Lugaresi E & Andermann F (1988) MELAS syndrome: characteristic migrainous and epileptic features and maternal transmission. Neurology 38, 751-4
DiMauro S, Zeviani M, Rizzuto R, Lombès A, Nakase H, Bonilla E, Miranda A & Schon E (1988) Molecular defects in cytochrome oxidase in mitochondrial diseases. J Bioenerg Biomembr 20, 353-64
Zeviani M, Sakoda S, Sherbany AA, Nakase H, Rizzuto R, Samitt CE, DiMauro S & Schon EA (1988) Sequence of cDNAs encoding subunit Vb of human and bovine cytochrome c oxidase. Gene 65, 1-11
Rizzuto R, Nakase H, Zeviani M, DiMauro S & Schon EA (1988) Subunit Va of human and bovine cytochrome c oxidase is highly conserved. Gene 69, 245-56
1987
Zeviani M, Peterson P, Servidei S, Bonilla E & DiMauro S (1987) Benign reversible muscle cytochrome c oxidase deficiency: a second case. Neurology 37, 64-7
DiMauro S, Servidei S, Zeviani M, Dirocco M, DeVivo DC, DiDonato S, Uziel G, Berry K, Hoganson G & Johnsen SD (1987) Cytochrome c oxidase deficiency in Leigh syndrome. Ann Neurol 22, 498-506
Zeviani M, Nakagawa M, Herbert J, Lomax MI, Grossman LI, Sherbany AA, Miranda AF, DiMauro S & Schon EA (1987) Isolation of a cDNA clone encoding subunit IV of human cytochrome c oxidase. Gene 55, 205-17
Servidei S, Lazaro RP, Bonilla E, Barron KD, Zeviani M & DiMauro S (1987) Mitochondrial encephalomyopathy and partial cytochrome c oxidase deficiency. Neurology 37, 58-63
DiMauro S, Bonilla E, Zeviani M, Servidei S, DeVivo DC & Schon EA (1987) Mitochondrial myopathies. J Inherit Metab Dis 10 Suppl 1, 113-28
Wood DS, Zeviani M, Prelle A, Bonilla E, Salviati G, Miranda AF, DiMauro S & Rowland LP (1987) Is nebulin the defective gene product in Duchenne muscular dystrophy?. N Engl J Med 316, 107-8
1986
DiMauro S, Zeviani M, Servidei S, Bonilla E, Miranda AF, Prelle A & Schon EA (1986) Cytochrome oxidase deficiency: clinical and biochemical heterogeneity. Ann N Y Acad Sci 488, 19-32
DiMauro S, Miranda AF, Sakoda S, Schon EA, Servidei S, Shanske S & Zeviani M (1986) Metabolic myopathies. Am J Med Genet 25, 635-51
Reichmann H, Rohkamm R, Zeviani M, Servidei S, Ricker K & DiMauro S (1986) Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration. Arch Neurol 43, 957-61
Zeviani M, Van Dyke DH, Servidei S, Bauserman SC, Bonilla E, Beaumont ET, Sharda J, VanderLaan K & DiMauro S (1986) Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiency. Arch Neurol 43, 1198-202
Herbert J, Wilcox JN, Pham KT, Fremeau RT, Zeviani M, Dwork A, Soprano DR, Makover A, Goodman DS & Zimmerman EA (1986) Transthyretin: a choroid plexus-specific transport protein in human brain. The 1986 S. Weir Mitchell award. Neurology 36, 900-11
1985
DiMauro S, Zeviani M, Bonilla E, Bresolin N, Nakagawa M, Miranda AF & Moggio M (1985) Cytochrome c oxidase deficiency. Biochem Soc Trans 13, 651-3
Betterle C, Caretto A, Zeviani M, Pedini B & Salviati C (1985) Demonstration and characterization of anti-human mitochondria autoantibodies in idiopathic hypoparathyroidism and in other conditions. Clin Exp Immunol 62, 353-60

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