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Mitochondrial disorders
Citations 1-10 of 85 total displayed.
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Most recent content
(9 Dec 2008):
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- ARTICLES
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction
- R. Del Bo, M. Moggio, M. Rango, S. Bonato, M. G. D’Angelo, S. Ghezzi, G. Airoldi, M. T. Bassi, M. Guglieri, L. Napoli, C. Lamperti, S. Corti, A. Federico, N. Bresolin, and G. P. Comi
Neurology 2008; 71: 1959-1966.
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Past content
(since Mar 2001):
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- ARTICLES
Diagnosing disconjugate eye movements: Phase-plane analysis of horizontal saccades
- Alessandro Serra, Ke Liao, Manuela Matta, and R. John Leigh
Neurology 2008; 71: 1167-1175.
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- ARTICLES
T2* and FSE MRI distinguishes four subtypes of neurodegeneration with brain iron accumulation
- A. McNeill, D. Birchall, S. J. Hayflick, A. Gregory, J. F. Schenk, E. A. Zimmerman, H. Shang, H. Miyajima, and P. F. Chinnery
Neurology 2008; 70: 1614-1619.
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- EDITORIALS
Dissecting brain death: Time for a new look
- Gustavo Saposnik and David G. Muñoz
Neurology 2008; 70: 1230-1231.
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- EDITORIALS
Myelin, mitochondria, and autoimmunity: What's the connection?
- Valerio Carelli and Marzio Bellan
Neurology 2008; 70: 1075-1076.
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- ARTICLES
Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus
- C. La Morgia, A. Achilli, L. Iommarini, P. Barboni, M. Pala, A. Olivieri, C. Zanna, S. Vidoni, C. Tonon, R. Lodi, R. Vetrugno, B. Mostacci, R. Liguori, R. Carroccia, P. Montagna, M. Rugolo, A. Torroni, and V. Carelli
Neurology 2008; 70: 762-770.
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- ARTICLES
Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease
- P. T. Luoma, J. Eerola, S. Ahola, A. H. Hakonen, O. Hellström, K. T. Kivistö, P. J. Tienari, and A. Suomalainen
Neurology 2007; 69: 1152-1159.
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- ARTICLES
Homoplasmy, heteroplasmy, and mitochondrial dystonia
- R. McFarland, P. F. Chinnery, E. L. Blakely, A. M. Schaefer, A.A.M. Morris, S. M. Foster, H. A.L. Tuppen, V. Ramesh, P. J. Dorman, D. M. Turnbull, and R. W. Taylor
Neurology 2007; 69: 911-916.
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- CLINICAL/SCIENTIFIC NOTES
LIMBIC ENCEPHALITIS AS PRESENTATION OF A SAP DEFICIENCY
- H. Verhelst, R. Van Coster, N. Bockaert, G. Laureys, S. Latour, A. Fischer, and F. Haerynck
Neurology 2007; 69: 218-219.
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- CLINICAL/SCIENTIFIC NOTES
MELAS ASSOCIATED WITH MUTATIONS IN THE POLG1 GENE
- M. Deschauer, S. Tennant, A. Rokicka, L. He, T. Kraya, D. M. Turnbull, S. Zierz, and R. W. Taylor
Neurology 2007; 68: 1741-1742.
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