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Mitochondrial disorders
Citations 71-80 of 92 total displayed.
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Past content
(since Mar 2001):
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- ARTICLES
Mitochondrial disorders: A proposal for consensus diagnostic criteria in infants and children
- Nicole I. Wolf and Jan A.M. Smeitink
Neurology 2002; 59: 1402-1405.
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- ARTICLES
Diagnostic criteria for respiratory chain disorders in adults and children
- F.P. Bernier, A. Boneh, X. Dennett, C.W. Chow, M.A. Cleary, and D.R. Thorburn
Neurology 2002; 59: 1406-1411.
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- ARTICLES
Mitochondrial DNA depletion: Mutations in thymidine kinase gene with myopathy and SMA
- M. Mancuso, L. Salviati, S. Sacconi, D. Otaegui, P. Camaño, A. Marina, S. Bacman, C.T. Moraes, J.R. Carlo, M. Garcia, M. Garcia-Alvarez, L. Monzon, A.B. Naini, M. Hirano, E. Bonilla, A.L. Taratuto, S. DiMauro, and T.H. Vu
Neurology 2002; 59: 1197-1202.
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- BRIEF COMMUNICATIONS
Ubiquinone and nicotinamide treatment of patients with the 3243A G mtDNA mutation
- A. M. Remes, E. V. Liimatta, S. Winqvist, U. Tolonen, J. A. Ranua, K. Reinikainen, I. E. Hassinen, and K. Majamaa
Neurology 2002; 59: 1275-1277.
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- CLINICAL/SCIENTIFIC NOTES
Mitochondrial complex I polymorphism and cigarette smoking in Parkinsons disease
- E.K. Tan, A. Chai, Y. Zhao, S.Y. Lum, S.M.C. Fook-Chong, M.L. Teoh, Y. Yih, R. Pavanni, and M.C. Wong
Neurology 2002; 59: 1288-a-1289-a.
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- ARTICLES
Neuronal hyperexcitability in stroke-like episodes of MELAS syndrome
- T. Iizuka, F. Sakai, N. Suzuki, T. Hata, S. Tsukahara, M. Fukuda, and Y. Takiyama
Neurology 2002; 59: 816-824.
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- BRIEF COMMUNICATIONS
Multiple mtDNA deletions with features of MNGIE
- J. Vissing, K. Ravn, E.R. Danielsen, M. Dunø, F. Wibrand, R.A. Wevers, and M. Schwartz
Neurology 2002; 59: 926-929.
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- BRIEF COMMUNICATIONS
Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL
- A. Malandrini, F. Albani, S. Palmeri, F. Fattapposta, S. Gambelli, G. Berti, A. Bracco, A. Tammaro, S. Calzavara, M. Villanova, M. Ferrari, A. Rossi, and P. Carrera
Neurology 2002; 59: 617-620.
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- BRIEF COMMUNICATIONS
Phenotypic variability in a Spanish family with MNGIE
- J. Gamez, C. Ferreiro, M. L. Accarino, L. Guarner, S. Tadesse, R. A. Martí, A. L. Andreu, N. Raguer, C. Cervera, and M. Hirano
Neurology 2002; 59: 455-457.
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- BRIEF COMMUNICATIONS
Brain aconitase activity is not decreased in progressive supranuclear palsy
- P. S. Fitzmaurice, C. L. Bamsey, L. Ang, M. Guttman, A. H. Rajput, Y. Furukawa, and S. J. Kish
Neurology 2002; 59: 137-138.
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