Advertisement
Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
 QUICK SEARCH:   [advanced]


     


Mitochondrial disorders

Citations 71-80 of 92 total displayed.

Past content (since Mar 2001):

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]  

ARTICLES
Mitochondrial DNA depletion: Mutations in thymidine kinase gene with myopathy and SMA
M. Mancuso, L. Salviati, S. Sacconi, D. Otaegui, P. Camaño, A. Marina, S. Bacman, C.T. Moraes, J.R. Carlo, M. Garcia, M. Garcia-Alvarez, L. Monzon, A.B. Naini, M. Hirano, E. Bonilla, A.L. Taratuto, S. DiMauro, and T.H. Vu
Neurology 2002; 59: 1197-1202. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Ubiquinone and nicotinamide treatment of patients with the 3243A->G mtDNA mutation
A. M. Remes, E. V. Liimatta, S. Winqvist, U. Tolonen, J. A. Ranua, K. Reinikainen, I. E. Hassinen, and K. Majamaa
Neurology 2002; 59: 1275-1277. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Mitochondrial complex I polymorphism and cigarette smoking in Parkinson’s disease
E.K. Tan, A. Chai, Y. Zhao, S.Y. Lum, S.M.C. Fook-Chong, M.L. Teoh, Y. Yih, R. Pavanni, and M.C. Wong
Neurology 2002; 59: 1288-a-1289-a. [Full text] [PDF]  

ARTICLES
Neuronal hyperexcitability in stroke-like episodes of MELAS syndrome
T. Iizuka, F. Sakai, N. Suzuki, T. Hata, S. Tsukahara, M. Fukuda, and Y. Takiyama
Neurology 2002; 59: 816-824. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Multiple mtDNA deletions with features of MNGIE
J. Vissing, K. Ravn, E.R. Danielsen, M. Dunø, F. Wibrand, R.A. Wevers, and M. Schwartz
Neurology 2002; 59: 926-929. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Asymptomatic cores and paracrystalline mitochondrial inclusions in CADASIL
A. Malandrini, F. Albani, S. Palmeri, F. Fattapposta, S. Gambelli, G. Berti, A. Bracco, A. Tammaro, S. Calzavara, M. Villanova, M. Ferrari, A. Rossi, and P. Carrera
Neurology 2002; 59: 617-620. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Phenotypic variability in a Spanish family with MNGIE
J. Gamez, C. Ferreiro, M. L. Accarino, L. Guarner, S. Tadesse, R. A. Martí, A. L. Andreu, N. Raguer, C. Cervera, and M. Hirano
Neurology 2002; 59: 455-457. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Brain aconitase activity is not decreased in progressive supranuclear palsy
P. S. Fitzmaurice, C. L. Bamsey, L. Ang, M. Guttman, A. H. Rajput, Y. Furukawa, and S. J. Kish
Neurology 2002; 59: 137-138. [Abstract] [Full text] [PDF]  

[First page]   [Previous page]   [Next page]
Pages: 1 2 3 4 5 6 7 8 9 10

* Collected Resources Home

* Related collections:
 Genetics
 All Genetics
 Neurofibromatosis
 Other neurocutaneous disorders
 Genetic linkage
 Association studies in genetics
 Gene expression studies
 Gene therapy
 Mitochondrial disorders
 Ion channel gene defects
 Spinocerebellar ataxia
 Trinucleotide repeat diseases
 Chromosomes


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH SEARCH RESULT
Copyright © 2009 by AAN Enterprises, Inc.
Advertisement