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Results:
1-7
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Results: 7
Authors:
Nishino, I
Spinazzola, A
Hirano, M
Citation: I. Nishino et al., MNGIE: from nuclear DNA to mitochondrial DNA, NEUROMUSC D, 11(1), 2001, pp. 7-10
Authors:
Manfredi, G
Spinazzola, A
Checcarelli, N
Naini, A
Citation: G. Manfredi et al., Assay of mitochondrial ATP synthesis in animal cells, METH CELL B, 65, 2001, pp. 133-145
Authors:
Di Giovanni, S
Mirabella, M
Spinazzola, A
Crociani, P
Silvestri, G
Broccolini, A
Tonali, P
Di Mauro, S
Servidei, S
Citation: S. Di Giovanni et al., Coenzyme Q(10) reverses pathological phenotype and reduces apoptosis in familial CoQ(10) deficiency, NEUROLOGY, 57(3), 2001, pp. 515-518
Authors:
Nishino, I
Spinazzola, A
Papadimitriou, A
Hammans, S
Steiner, I
Hahn, CD
Connolly, AM
Verloes, A
Guimaraes, J
Maillard, I
Hamano, H
Donati, MA
Semrad, CE
Russell, JA
Andreu, AL
Hadjigeorgiou, GM
Vu, TH
Tadesse, S
Nygaard, TG
Nonaka, I
Hirano, I
Bonilla, E
Rowland, LP
DiMauro, S
Hirano, M
Citation: I. Nishino et al., Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations, ANN NEUROL, 47(6), 2000, pp. 792-800
Authors:
Nishino, I
Spinazzola, A
Hirano, M
Citation: I. Nishino et al., Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder, SCIENCE, 283(5402), 1999, pp. 689-692
Authors:
Servidei, S
Capon, F
Spinazzola, A
Mirabella, M
Semprini, S
de Rosa, G
Gennarelli, M
Sangiuolo, F
Ricci, E
Mohrenweiser, HW
Dallapiccola, B
Tonali, P
Novelli, G
Citation: S. Servidei et al., A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13, NEUROLOGY, 53(4), 1999, pp. 830-837
Authors:
Manfred, G
Gupta, N
Vazquez-Memije, ME
Sadlock, JE
Spinazzola, A
De Vivo, DC
Schon, EA
Citation: G. Manfred et al., Oligomycin induces a decrease in the cellular content of a pathogenic mutation in the human mitochondrial ATPase 6 gene, J BIOL CHEM, 274(14), 1999, pp. 9386-9391
Risultati:
1-7
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