|
Leukodystrophies
Citations 11-20 of 51 total displayed.
|
Past content
(since Jan 2001):
|
- NEUROIMAGES
Progressive multifocal leukoencephalopathy with selective involvement of the pyramidal tracts
- Alexander Semmler, Horst Urbach, Thomas Klockgether, and Michael Linnebank
Neurology 2007; 68: 871.
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Peripheral and central hypomyelination with hypogonadotropic hypogonadism and hypodontia
- M. Timmons, M. Tsokos, M. Abu Asab, S. B. Seminara, G. C. Zirzow, C. R. Kaneski, J. D. Heiss, M. S. van der Knaap, M. T. Vanier, R. Schiffmann, and K. Wong
Neurology 2006; 67: 2066-2069.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
An adult case of leukoencephalopathy with intracranial calcifications and cysts
- John R. Corboy, Judith Gault, and B. K. Kleinschmidt-DeMasters
Neurology 2006; 67: 1890-1892.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
3-Methylglutaconic aciduria type I causes leukoencephalopathy of adult onset
- M. Eriguchi, H. Mizuta, K. Kurohara, M. Kosugi, Y. Yakushiji, R. Okada, M. Yukitake, Y. Hasegawa, S. Yamaguchi, and Y. Kuroda
Neurology 2006; 67: 1895-1896.
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Leukoencephalopathy induced by levamisole alone for the treatment of recurrent aphthous ulcers
- H. M. Liu, W. J. Hsieh, C. C. Yang, V. C. Wu, and K. D. Wu
Neurology 2006; 67: 1065-1067.
[Abstract]
[Full text]
[PDF]
- ARTICLES
Late-onset metachromatic leukodystrophy: Genotype strongly influences phenotype
- H. Rauschka, B. Colsch, N. Baumann, R. Wevers, M. Schmidbauer, M. Krammer, J. -C. Turpin, M. Lefevre, C. Olivier, S. Tardieu, W. Krivit, H. Moser, A. Moser, V. Gieselmann, B. Zalc, T. Cox, U. Reuner, A. Tylki-Szymanska, F. Aboul-Enein, E. LeGuern, H. Bernheimer, and J. Berger
Neurology 2006; 67: 859-863.
[Abstract]
[Full text]
[PDF]
- ARTICLES
A new type of leukoencephalopathy with metaphyseal chondrodysplasia maps to Xq25-q27
- B. A. Neubauer, I. Stefanova, C. A. Hübner, E. Neumaier-Probst, J. Bohl, H. C. Oppermann, H. Stöß, A. Hahn, U. Stephani, A. Kohlschütter, and A. Gal
Neurology 2006; 67: 587-591.
[Abstract]
[Full text]
[PDF]
- CLINICAL/SCIENTIFIC NOTES
Early MR imaging and spectroscopy appearance of eIF2B-related leukoencephalopathy
- M. Mascalchi, D. De Grandis, A. Ginestroni, A. Pratesi, R. Della Nave, G. C. Scheper, and M. S. van der Knaap
Neurology 2006; 67: 537-538.
[Full text]
[PDF]
- ARTICLES
GJA12 mutations in children with recessive hypomyelinating leukoencephalopathy
- M. Bugiani, S. Al Shahwan, E. Lamantea, A. Bizzi, E. Bakhsh, I. Moroni, M. R. Balestrini, G. Uziel, and M. Zeviani
Neurology 2006; 67: 273-279.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Peripheral neuropathy in vanishing white matter disease with a novel EIF2B5 mutation
- A. Federico, O. Scali, M. L. Stromillo, C. Di Perri, S. Bianchi, F. Sicurelli, N. De Stefano, A. Malandrini, and M. T. Dotti
Neurology 2006; 67: 353-355.
[Abstract]
[Full text]
[PDF]
|
|
