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All Genetics
Citations 201-210 of 676 total displayed.
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Past content
(since Jan 2001):
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- NEUROIMAGES
Microhemorrhages in a patient with reversible posterior leukoencephalopathy syndrome
- H. Kawai, H. Nakamura, M. Sanada, S. Kitahara, and K. Maeda
Neurology 2006; 67: 1712.
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- ARTICLES
Family history of stroke and severity of neurologic deficit after stroke
- J. F. Meschia, L. D. Case, B. B. Worrall, R. D. Brown, Jr, T. G. Brott, M. Frankel, S. Silliman, S. S. Rich for the Ischemic Stroke Genetics Study Group
Neurology 2006; 67: 1396-1402.
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- BRIEF COMMUNICATIONS
Diagnostic challenges in facioscapulohumeral muscular dystrophy
- S. Sacconi, L. Salviati, I. Bourget, D. Figarella, Y. Péréon, R. Lemmers, S. van der Maarel, and C. Desnuelle
Neurology 2006; 67: 1464-1466.
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- BRIEF COMMUNICATIONS
Parkinsonism, Lrrk2 G2019S, and tau neuropathology
- A. Rajput, D. W. Dickson, C. A. Robinson, O. A. Ross, J. C. Dächsel, S. J. Lincoln, S. A. Cobb, M. L. Rajput, and M. J. Farrer
Neurology 2006; 67: 1506-1508.
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- CLINICAL/SCIENTIFIC NOTES
LRRK2 mutations on Crete: R1441H associated with PD evolving to PSP
- Cleanthe Spanaki, Helen Latsoudis, and Andreas Plaitakis
Neurology 2006; 67: 1518-1519.
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- ARTICLES
SMN1 gene, but not SMN2, is a risk factor for sporadic ALS
- P. Corcia, W. Camu, J. -M. Halimi, P. Vourc'h, C. Antar, S. Vedrine, B. Giraudeau, B. de Toffol, C. R. Andres for The French ALS Study Group
Neurology 2006; 67: 1147-1150.
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- ARTICLES
Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutations
- J. S. Müller, S. K. Baumeister, V. M. Rasic, S. Krause, S. Todorovic, K. Kugler, W. Müller-Felber, A. Abicht, and H. Lochmüller
Neurology 2006; 67: 1159-1164.
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- BRIEF COMMUNICATIONS
Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese
- Y. Onodera, M. Aoki, H. Mizuno, H. Warita, Y. Shiga, and Y. Itoyama
Neurology 2006; 67: 1300-1302.
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- BRIEF COMMUNICATIONS
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)
- N. Parkinson, P. G. Ince, M. O. Smith, R. Highley, G. Skibinski, P. M. Andersen, K. E. Morrison, H. S. Pall, O. Hardiman, J. Collinge, P. J. Shaw, EM C. Fisher on behalf of the MRC Proteomics in ALS Study and the FReJA Consortium
Neurology 2006; 67: 1074-1077.
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- BRIEF COMMUNICATIONS
Hypokalemic paralysis due to Gitelman syndrome: A family study
- H. -Y. Ng, S. -H. Lin, C. -Y. Hsu, Y. -Z. Tsai, H. -C. Chen, and C. -T. Lee
Neurology 2006; 67: 1080-1082.
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