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Mitochondrial disorders
Citations 21-30 of 92 total displayed.
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Past content
(since Mar 2001):
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- BRIEF COMMUNICATIONS
POLG1 in idiopathic Parkinson disease
- W. Tiangyou, G. Hudson, D. Ghezzi, G. Ferrari, M. Zeviani, D. J. Burn, and P. F. Chinnery
Neurology 2006; 67: 1698-1700.
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- CLINICAL/SCIENTIFIC NOTES
Absence of cognitive, behavioral, or emotional dysfunction in progressive muscular atrophy
- P. Wicks, S. Abrahams, P. N. Leigh, T. Williams, and L. H. Goldstein
Neurology 2006; 67: 1718-1719.
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- BRIEF COMMUNICATIONS
Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE
- M. Hirano, R. Martí, C. Casali, S. Tadesse, T. Uldrick, B. Fine, D. M. Escolar, M. L. Valentino, I. Nishino, C. Hesdorffer, J. Schwartz, R. G. Hawks, D. L. Martone, M. S. Cairo, S. DiMauro, M. Stanzani, J. H. Garvin, Jr, and D. G. Savage
Neurology 2006; 67: 1458-1460.
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- BRIEF COMMUNICATIONS
Infusion of platelets transiently reduces nucleoside overload in MNGIE
- M. C. Lara, B. Weiss, I. Illa, P. Madoz, L. Massuet, A. L. Andreu, M. L. Valentino, Y. Anikster, M. Hirano, and R. Martí
Neurology 2006; 67: 1461-1463.
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- CLINICAL/SCIENTIFIC NOTES
Late-onset multiple acyl-CoA dehydrogenase deficiency: A frequently missed diagnosis?
- S. Köppel, J. Gottschalk, G. F. Hoffmann, H. R. Waterham, H. Blobel, and S. Kölker
Neurology 2006; 67: 1519.
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- BRIEF COMMUNICATIONS
Progressive depletion of mtDNA in mitochondrial myopathy
- Steve E. Durham, Denise T. Brown, Douglass M. Turnbull, and Patrick F. Chinnery
Neurology 2006; 67: 502-504.
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- BRIEF COMMUNICATIONS
Mitochondrial disease in adults: A scale to monitor progression and treatment
- A. M. Schaefer, C. Phoenix, J. L. Elson, R. McFarland, P. F. Chinnery, and D. M. Turnbull
Neurology 2006; 66: 1932-1934.
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- BRIEF COMMUNICATIONS
Endothelial dysfunction in MELAS improved by l-arginine supplementation
- Y. Koga, Y. Akita, N. Junko, S. Yatsuga, N. Povalko, R. Fukiyama, M. Ishii, and T. Matsuishi
Neurology 2006; 66: 1766-1769.
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- ARTICLES
A 3-year clinical follow-up of adult patients with 3243A>G in mitochondrial DNA
- K.A.M. Majamaa-Voltti, S. Winqvist, A. M. Remes, U. Tolonen, J. Pyhtinen, S. Uimonen, M. Kärppä, M. Sorri, K. Peuhkurinen, and K. Majamaa
Neurology 2006; 66: 1470-1475.
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- BRIEF COMMUNICATIONS
POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions
- G. Hudson, M. Deschauer, R. W. Taylor, M. G. Hanna, D. Fialho, A. M. Schaefer, L. -P. He, E. Blakely, D. M. Turnbull, and P. F. Chinnery
Neurology 2006; 66: 1439-1441.
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