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Leukodystrophies
Citations 41-50 of 51 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Indian Agarwal megalencephalic leukodystrophy with cysts is caused by a common MLC1 mutation
- J. R. Gorospe, B. S. Singhal, T. Kainu, F. Wu, D. Stephan, J. Trent, E. P. Hoffman, and S. Naidu
Neurology 2004; 62: 878-882.
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- ARTICLES
Membrane phospholipids and high-energy metabolites in childhood ataxia with CNS hypomyelination
- S. Blüml, M. Philippart, R. Schiffmann, K. Seymour, and B. D. Ross
Neurology 2003; 61: 648-654.
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- BRIEF COMMUNICATIONS
A randomized controlled study of modified cobratoxin in adrenomyeloneuropathy
- H.R. Mundy, S.J. Jones, J.C. Hobart, M.G. Hanna, and P.J. Lee
Neurology 2003; 61: 528-530.
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- ARTICLES
Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy
- D. J. Loes, A. Fatemi, E. R. Melhem, N. Gupte, L. Bezman, H. W. Moser, and G. V. Raymond
Neurology 2003; 61: 369-374.
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- BRIEF COMMUNICATIONS
Canavan’s leukodystrophy is associated with defects in cochlear neurodevelopment and deafness
- Gail Ishiyama, Ivan Lopez, Robert W. Baloh, and Akira Ishiyama
Neurology 2003; 60: 1702-1704.
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- NEUROIMAGES
MNGIE: Diarrhea and leukoencephalopathy
- P. Labauge, R. Durant, G. Castelnovo, and A. Dubois
Neurology 2002; 58: 1862.
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- EDITORIALS
Intermediate filament proteinopathies: From cytoskeletons to genes to functional nosology
- William D. Graf and Harvey B. Sarnat
Neurology 2002; 58: 1451-1453.
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- ARTICLES
Molecular findings in symptomatic and pre-symptomatic Alexander disease patients
- J. R. Gorospe, S. Naidu, A. B. Johnson, V. Puri, G. V. Raymond, S. D. Jenkins, R. C. Pedersen, D. Lewis, P. Knowles, R. Fernandez, D. De Vivo, M. S. van der Knaap, A. Messing, M. Brenner, and E. P. Hoffman
Neurology 2002; 58: 1494-1500.
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- ARTICLES
Proton MR spectroscopic imaging predicts lesion progression on MRI in X-linked adrenoleukodystrophy
- F. S. Eichler, P. B. Barker, C. Cox, D. Edwin, A. M. Ulug, H. W. Moser, and G. V. Raymond
Neurology 2002; 58: 901-907.
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- VIEWS & REVIEWS
Late onset white matter disease in peroxisome biogenesis disorder
- P.G. Barth, J. Gootjes;, H. Bode, P. Vreken, C.B.L.M. Majoie, and R.J.A. Wanders
Neurology 2001; 57: 1949-1955.
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