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Toxic myopathy with rhabdomyolysis after quail poisoning 1-gen-1997 Musumeci, Olimpia; Toscano, Antonio; Aguennouz, M'Hammed; M. C., Monici; Gallitto, Giuseppe; Tisano, Adriana; Rodolico, Carmelo; M., Valenti
A cytochemical study of apoptosis in metabolic myopathies 1-gen-1997 Monici, Mc; Migliorato, A; Toscano, Antonio; Musumeci, Olimpia; Aguennouz, M'Hammed; Vita, G.
A benign case of congenital myotonic dystrophy 1-gen-1998 Musumeci, Olimpia; Toscano, Antonio; Condorelli, D; Trovato Salinaro, A; Spinella, F; Cordaro, S; Bonsignore, M; Vita, G.
Central and perypheral nervous system involvement in hereditary coproporphyria. 1-gen-1998 Rodolico, Carmelo; Toscano, Antonio; Valenti, M.; Musumeci, Olimpia; Macaione, Vincenzo; Vita, Giuseppe
Apoptosis in metabolic myopathies 1-gen-1998 Monici, Mc; Toscano, Antonio; Girlanda, Paolo; Aguennouz, M'Hammed; Musumeci, Olimpia; Vita, Giuseppe
Lipid peroxidation, free radicals and antioxidants in patients with myotonic distrophy. 1-gen-1999 Toscano, Antonio; Annesi, G.; Campo, Giuseppe Maurizio; Musumeci, Olimpia; Rodolico, Carmelo; Spadafora, P.; Pasqua, A. A.; Annesi, F.; Annesi, A.; Caputi, A.; Vita, G. .
Power spectral analysis of heart rate in myotonic dystrophy 1-gen-1999 Di Leo, R; Vita, G.; Rodolico, Carmelo; Musumeci, Olimpia; Toscano, Antonio; Messina, C.
A novel mutation in the mitochondrial DNA transfer ribonucleic acidAsp gene in a child with myoclonic epilepsy and psychomotor regression. 1-gen-1999 Shtilbans, A; El Schahawi, M; Malkin, E; Shanske, S; Musumeci, Olimpia; Dimauro, S.
Clinical eterogeneity and molecular basis of myoadenilate deaminase deficiency. 1-gen-2000 Aguennouz, M'Hammed; Rodolico, Carmelo; Ciranni, A; Migliorato, A; Musumeci, Olimpia; Vita, G; Toscano, Antonio
Clinical hetrogeneity and molecular basis of myoadenilate deaminase deficiency 1-gen-2000 Aguennouz, M'Hammed; Rodolico, Carmelo; Ciranni, A; Migliorato, A; Musumeci, Olimpia; Vita, G; Toscano, Antonio
Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathy. 1-gen-2000 Musumeci, Olimpia; Andreu, Al; Shanske, S; Bresolin, N; Comi, Gp; Rothstein, R; Schon, Ea; Dimauro, S.
Clinical spectrum of muscle Coenzyme Q10 deficiency 1-gen-2000 Musumeci, Olimpia; Hirano, M; Naini, A; Shanske, S; Dimauro, S.
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle disease. 1-gen-2000 Fernández, R; Navarro, C; Andreu, Al; Bruno, C; Shanske, S; Gámez, J; Teijeira, S; Hernández, I; Teijeiro, A; Fernández, Jm; Musumeci, Olimpia; Dimauro, S.
MELAS-like phenotype in a patient with complex III deficiency and a new cytochrome b mutation 1-gen-2001 Musumeci, Olimpia; Hadjigeorgiou, Gm; Garcia Alvarez, M; Pallotti, F; Krishna, S; Shanske, S; Dimauro, S.
Calpain 3 expression in limb-girdle muscular dystrophy type 2A (LGMD 2A). 1-gen-2001 Aguennouz, M'Hammed; Monici, Mc; Musumeci, Olimpia; Rodolico, Carmelo; Ciranni, A; Toscano, Antonio; Vita, G.
Skeletal muscle lipid storage and mitochondrial beta-oxidation. 1-gen-2001 Toscano, Antonio; Aguennouz, M'Hammed; Rodolico, Carmelo; Ciranni, A; Autunno, M; Musumeci, Olimpia; Vita, G.
Clinical heterogeneity and molecular basis of myoadenilate deaminase deficiency 1-gen-2001 Aguennouz, M'Hammed; Rodolico, Carmelo; Ciranni, A; Migliorato, A; Musumeci, Olimpia; Vita, G; Toscano, Antonio
Diseases of oxidative phosphorylation due to mtDNA mutations. 1-gen-2001 Dimauro, S; Andreu, Al; Musumeci, Olimpia; Bonilla, E.
Coenzyme Q10 deficiency in previously unclassified cerebellar ataxia 1-gen-2001 Musumeci, Olimpia; Naini, A; Slonim, Ae; Tsao, Cy; Mendell, Jr; De Vivo, Dc; Hirano, M; Dimauro, S.
Surprises of genetic engineering: a possible model of polyglucosan body disease. 1-gen-2001 Raben, N; Danon, M; Lu, N; Lee, E; Shliselfeld, L; Skurat, Av; Roach, Pj; Lawrence JC, Jr; Musumeci, Olimpia; Shanske, S; Dimauro, S; Plotz, P.
Mostrati risultati da 1 a 20 di 260
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