Mitochondrial disorders; see Genetics/Mitochondrial disorders

Citations 1-6 of 6 total displayed.

Most recent content (11 Sep 2007):

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]  

Past content (since Nov 2002):

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
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]  

ARTICLES
Prevalence of multiple sclerosis in a residential area bordering an oil refinery

J. S. Neuberger, S. G. Lynch, M. L. Sutton, S. B. Hall, C. Feng, and W. R. Schmidt
Neurology 2004; 63: 1796-1802. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]