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Zeviani M, Bresolin N, Gellera C, Bordoni A, Pannacci M, Amati P, Moggio M, Servidei S, Scarlato G & DiDonato S (1990) Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease. Am J Hum Genet 47, 904-14
Zeviani M, Servidei S, Gellera C, Bertini E, DiMauro S & DiDonato S (1989) An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region. Nature 339, 309-11
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
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
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
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
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
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
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
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
Bresolin N, Zeviani M, Bonilla E, Miller RH, Leech RW, Shanske S, Nakagawa M & DiMauro S (1985) Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle. Neurology 35, 802-12
Schmoldt A, Benthe HF & Haberland G (1975) Digitoxin metabolism by rat liver microsomes. Biochem Pharmacol 24, 1639-41