Mitochondrial disorders

Citations 1-10 of 82 total displayed.

Most recent content (29 Apr 2008):

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. [Abstract] [Full text] [PDF]  

Past content (since Mar 2001):

EDITORIALS
Dissecting brain death: Time for a new look

Gustavo Saposnik and David G. Muñoz
Neurology 2008; 70: 1230-1231. [Full text] [PDF]  

EDITORIALS
Myelin, mitochondria, and autoimmunity: What's the connection?

Valerio Carelli and Marzio Bellan
Neurology 2008; 70: 1075-1076. [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Full text] [PDF]  

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. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Tetracycline delays ocular motility decline in chronic progressive external ophthalmoplegia

Ayman Omar and Lenworth N. Johnson
Neurology 2007; 68: 1159-1160. [Full text] [PDF]  

ARTICLES
Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNA^Lys

Rita Horvath, Rudolf Andre Kley, Hanns Lochmüller, and Matthias Vorgerd
Neurology 2007; 68: 56-58. [Abstract] [Full text] [PDF]  

ARTICLES
Mitochondrial disease criteria: Diagnostic applications in children

E. Morava, L. van den Heuvel, F. Hol, M. C. de Vries, M. Hogeveen, R. J. Rodenburg, and J.A.M. Smeitink
Neurology 2006; 67: 1823-1826. [Abstract] [Full text] [PDF]  

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