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All Genetics
Citations 21-30 of 679 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Cognitive impairment and reduced life span of oculopharyngeal muscular dystrophy homozygotes
- S. C. Blumen, J. -P. Bouchard, B. Brais, R. L. Carasso, D. Paleacu, V. E. Drory, S. Chantal, N. Blumen, and I. Braverman
Neurology 2009; 73: 596-601.
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- ARTICLES
Parent-of-origin effect in multiple sclerosis: Observations from interracial matings
- S. V. Ramagopalan, I. M. Yee, D. A. Dyment, S. -M. Orton, R. A. Marrie, A. D. Sadovnick, G. C. Ebers For the Canadian Collaborative Study Group
Neurology 2009; 73: 602-605.
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- ARTICLES
Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His
- J. van der Zee, D. Pirici, T. Van Langenhove, S. Engelborghs, R. Vandenberghe, M. Hoffmann, G. Pusswald, M. Van den Broeck, K. Peeters, M. Mattheijssens, J. -J. Martin, P. P. De Deyn, M. Cruts, D. Haubenberger, S. Kumar-Singh, A. Zimprich, and C. Van Broeckhoven
Neurology 2009; 73: 626-632.
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- ARTICLES
Consequences of mutations within the C terminus of the FHL1 gene
- B. Schoser, H. H. Goebel, I. Janisch, S. Quasthoff, J. Rother, M. Bergmann, W. Müller-Felber, and C. Windpassinger
Neurology 2009; 73: 543-551.
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- EDITORIALS
Ataxia-telangiectasia: Without ataxia or telangiectasia?
- Rachel J. Saunders-Pullman and Richard Gatti
Neurology 2009; 73: 414-415.
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- ARTICLES
Clinical spectrum of ataxia-telangiectasia in adulthood
- M.M.M. Verhagen, W. F. Abdo, M. A.A.P. Willemsen, F. B.L. Hogervorst, D. F.C.M. Smeets, J. A.P. Hiel, E. R. Brunt, M. A. van Rijn, D. Majoor Krakauer, R. A. Oldenburg, A. Broeks, J. I. Last, L. J. van’t Veer, M. A.J. Tijssen, A. M.I. Dubois, H. P.H. Kremer, C. M.R. Weemaes, A. M.R. Taylor, and M. van Deuren
Neurology 2009; 73: 430-437.
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- EDITORIALS
Multiple sclerosis. Evidence of maternal effects and an increasing incidence in women
- John W. Rose
Neurology first published on July 29, 2009 as doi: WNL.0b013e3181b529c6.
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- EDITORIALS
Ataxia-telangiectasia. Without ataxia or telangiectasia?
- Rachel J. Saunders-Pullman and Richard Gatti
Neurology first published on July 15, 2009 as doi: WNL.0b013e3181b39140.
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- CLINICAL/SCIENTIFIC NOTES
CEREBELLAR SIGNS IN CELIAC DISEASE
- M. Versino, D. Franciotta, S. Colnaghi, F. Biagi, E. Zardini, P. I. Bianchi, G. R. Corazza, and V. Cosi
Neurology 2009; 72: 2046-2048.
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- ARTICLES
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy
- M. C. Hannibal, E. K. Ruzzo, L. R. Miller, B. Betz, J. G. Buchan, D. M. Knutzen, K. Barnett, M. L. Landsverk, A. Brice, E. LeGuern, H. M. Bedford, B. B. Worrall, S. Lovitt, S. H. Appel, E. Andermann, T. D. Bird, and P. F. Chance
Neurology 2009; 72: 1755-1759.
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