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All Genetics
Citations 31-40 of 679 total displayed.
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Past content
(since Jan 2001):
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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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- CLINICAL/SCIENTIFIC NOTES
DYSTONIC TREMOR PRESENTING AS PARKINSONISM: LONG-TERM FOLLOW-UP OF SWEDDs
- Peter G. Bain
Neurology 2009; 72: 1443-1445.
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- NEUROIMAGES
The small, spastic, and furrowed tongue of Allgrove syndrome
- Henry Houlden
Neurology 2009; 72: 1366.
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- ARTICLES
The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome
- B. Ben Zeev, A. Bebbington, G. Ho, H. Leonard, N. de Klerk, E. Gak, M. Vecksler, and J. Christodoulou
Neurology 2009; 72: 1242-1247.
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- ARTICLES
Etiology of musician’s dystonia: Familial or environmental?
- A. Schmidt, H. -C. Jabusch, E. Altenmüller, J. Hagenah, N. Brüggemann, K. Lohmann, L. Enders, P. L. Kramer, R. Saunders-Pullman, S. B. Bressman, A. Münchau, and C. Klein
Neurology 2009; 72: 1248-1254.
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- ARTICLES
A mechanism for low penetrance in an ALS family with a novel SOD1 deletion
- L. Zinman, H. N. Liu, C. Sato, Y. Wakutani, A. F. Marvelle, D. Moreno, K. E. Morrison, K. L. Mohlke, J. Bilbao, J. Robertson, and E. Rogaeva
Neurology 2009; 72: 1153-1159.
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- ARTICLES
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H
- G. M. Fabrizi, F. Taioli, T. Cavallaro, S. Ferrari, L. Bertolasi, M. Casarotto, N. Rizzuto, T. Deconinck, V. Timmerman, and P. De Jonghe
Neurology 2009; 72: 1160-1164.
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- CLINICAL/SCIENTIFIC NOTES
GLUCOCEREBROSIDASE MUTATIONS IN 108 NEUROPATHOLOGICALLY CONFIRMED CASES OF MULTIPLE SYSTEM ATROPHY
- B. Segarane, A. Li, R. Paudel, S. Scholz, J. Neumann, A. Lees, T. Revesz, J. Hardy, C. J. Mathias, N. W. Wood, J. Holton, and H. Houlden
Neurology 2009; 72: 1185-1186.
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