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Mitochondrial disorders
Citations 31-40 of 92 total displayed.
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Past content
(since Mar 2001):
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- ARTICLES
Dichloroacetate causes toxic neuropathy in MELAS: A randomized, controlled clinical trial
- P. Kaufmann, K. Engelstad, Y. Wei, S. Jhung, M. C. Sano, D. C. Shungu, W. S. Millar, X. Hong, C. L. Gooch, X. Mao, J. M. Pascual, M. Hirano, P. W. Stacpoole, S. DiMauro, and D. C. De Vivo
Neurology 2006; 66: 324-330.
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- BRIEF COMMUNICATIONS
Coenzyme Q10 deficiency and isolated myopathy
- R. Horvath, P. Schneiderat, B.G.H. Schoser, K. Gempel, E. Neuen-Jacob, H. Plöger, J. Müller-Höcker, D. E. Pongratz, A. Naini, S. DiMauro, and H. Lochmüller
Neurology 2006; 66: 253-255.
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- RESIDENT AND FELLOW PAGE
Symmetric basal ganglia calcification in a 9-year-old child with MELAS
- Sheng-Horng Chung, Shyr-Chyr Chen, Wen-Jone Chen, and Chien-Chang Lee
Neurology 2005; 65: E19.
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- BRIEF COMMUNICATIONS
POLG mutations in Alpers syndrome
- K. V. Nguyen, E. Østergaard, S. Holst Ravn, T. Balslev, E. Rubæk Danielsen, A. Vardag, P. J. McKiernan, G. Gray, and R. K. Naviaux
Neurology 2005; 65: 1493-1495.
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- BRIEF COMMUNICATIONS
Mitochondrial DNA copy number threshold in mtDNA depletion myopathy
- S. E. Durham, E. Bonilla, D. C. Samuels, S. DiMauro, and P. F. Chinnery
Neurology 2005; 65: 453-455.
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- ARTICLES
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase  mutations
- S. Winterthun, G. Ferrari, L. He, R. W. Taylor, M. Zeviani, D. M. Turnbull, B. A. Engelsen, G. Moen, and L. A. Bindoff
Neurology 2005; 64: 1204-1208.
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- EDITORIALS
Optic mitochondriopathies
- Patrick F. Chinnery and Philip G. Griffiths
Neurology 2005; 64: 940-941.
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- ARTICLES
Mitochondrial DNA content is decreased in autosomal dominant optic atrophy
- J. Y. Kim, J.-M. Hwang, H. S. Ko, M.-W. Seong, B.-J. Park, and S. S. Park
Neurology 2005; 64: 966-972.
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- ARTICLES
Prevalence of large-scale mitochondrial DNA deletions in an adult Finnish population
- A. M. Remes, K. Majamaa-Voltti, M. Kärppä, J. S. Moilanen, S. Uimonen, H. Helander, H. Rusanen, P. I. Salmela, M. Sorri, I. E. Hassinen, and K. Majamaa
Neurology 2005; 64: 976-981.
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- CLINICAL/SCIENTIFIC NOTES
Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intolerance
- T. Pulkes, D. Liolitsa, A. J. Wills, I. Hargreaves, S. Heales, and M. G. Hanna
Neurology 2005; 64: 1091-1092.
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