|
All Genetics
Citations 201-210 of 679 total displayed.
|
Past content
(since Jan 2001):
|
- BRIEF COMMUNICATIONS
Phenotypic homogeneity of the Huntington disease–like presentation in a SCA17 family
- S. A. Schneider, B.P.C. van de Warrenburg, T. D. Hughes, M. Davis, M. Sweeney, N. Wood, N. P. Quinn, and K. P. Bhatia
Neurology 2006; 67: 1701-1703.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Genetic heterogeneity of autosomal dominant nonprogressive congenital ataxia
- J. C. Jen, H. Lee, Y. H. Cha, S. F. Nelson, and R. W. Baloh
Neurology 2006; 67: 1704-1706.
[Abstract]
[Full text]
[PDF]
- BRIEF COMMUNICATIONS
Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura
- U. Todt, J. Freudenberg, I. Goebel, A. Heinze, K. Heinze-Kuhn, M. Rietschel, H. Göbel, and C. Kubisch
Neurology 2006; 67: 1707-1709.
[Abstract]
[Full text]
[PDF]
- 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.
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
|
|
