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All Genetics
Citations 21-30 of 676 total displayed.
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Past content
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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.
Rapid PDF
- 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.
Rapid PDF
- 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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- ARTICLES
Age and founder effect of SOD1 A4V mutation causing ALS
- M. Saeed, Y. Yang, H-X Deng, W-Y Hung, N. Siddique, L. Dellefave, C. Gellera, P. M. Andersen, and T. Siddique
Neurology 2009; 72: 1634-1639.
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- ARTICLES
Reduced frequency of ALS in an ethnically mixed population: A population-based mortality study
- T. Zaldivar, J. Gutierrez, G. Lara, M. Carbonara, G. Logroscino, and O. Hardiman
Neurology 2009; 72: 1640-1645.
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- ARTICLES
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes
- M. Fanin, A. C. Nascimbeni, S. Aurino, E. Tasca, E. Pegoraro, V. Nigro, and C. Angelini
Neurology 2009; 72: 1432-1435.
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