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Neurology
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Amyotrophic lateral sclerosis

Citations 11-20 of 223 total displayed.

Past content (since Jan 2001):

MEDICAL HYPOTHESIS
ALS motor phenotype heterogeneity, focality, and spread: Deconstructing motor neuron degeneration
John M. Ravits and Albert R. La Spada
Neurology 2009; 73: 805-811. [Abstract] [Full text] [PDF]  

EDITORIALS
Paraoxonase genes and susceptibility to ALS
David A. Greenberg, William C.L. Stewart, and Lewis P. Rowland
Neurology 2009; 73: 11-12. [Full text] [PDF]  

ARTICLES
Characterization of DCTN1 genetic variability in neurodegeneration
C. Vilariño-Güell, C. Wider, A. I. Soto-Ortolaza, S. A. Cobb, J. M. Kachergus, B. H. Keeling, J. C. Dachsel, M. M. Hulihan, D. W. Dickson, Z. K. Wszolek, R. J. Uitti, N. R. Graff-Radford, B. F. Boeve, K. A. Josephs, B. Miller, K. B. Boylan, K. Gwinn, C. H. Adler, J. O. Aasly, F. Hentati, A. Destée, A. Krygowska-Wajs, M. -C. Chartier-Harlin, O. A. Ross, R. Rademakers, and M. J. Farrer
Neurology 2009; 72: 2024-2028. [Abstract] [Full text] [PDF]  

ARTICLES
Clinical features that distinguish PLS, upper motor neuron–dominant ALS, and typical ALS
P. H. Gordon, B. Cheng, I. B. Katz, H. Mitsumoto, and L. P. Rowland
Neurology 2009; 72: 1948-1952. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

ARTICLES
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
I. Le Ber, A. Camuzat, E. Berger, D. Hannequin, A. Laquerrière, V. Golfier, D. Seilhean, G. Viennet, P. Couratier, P. Verpillat, S. Heath, W. Camu, O. Martinaud, L. Lacomblez, M. Vercelletto, F. Salachas, F. Sellal, M. Didic, C. Thomas-Anterion, M. Puel, B-F Michel, C. Besse, C. Duyckaerts, V. Meininger, D. Campion, B. Dubois, A. Brice For the French Research Network on FTD/FTD-MND
Neurology 2009; 72: 1669-1676. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
RECURRENT PERICARDITIS DUE TO NATALIZUMAB TREATMENT
Mikael Cohen, Fanny Rocher, Claude Brunschwig, and Christine Lebrun
Neurology 2009; 72: 1616-1617. [Full text] [PDF]  

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. [Full text] [PDF]  

ARTICLES
Natural history and clinical features of the flail arm and flail leg ALS variants
L. C. Wijesekera, S. Mathers, P. Talman, C. Galtrey, M. H. Parkinson, J. Ganesalingam, E. Willey, M. A. Ampong, C. M. Ellis, C. E. Shaw, A. Al-Chalabi, and P. N. Leigh
Neurology 2009; 72: 1087-1094. [Abstract] [Full text] [PDF]  

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* Collected Resources Home

* Related collections:
 Neuromuscular disease
 All Neuromuscular Disease
 Anterior nerve cell disease
 Amyotrophic lateral sclerosis
 Myasthenia
 Lambert-Eaton syndrome
 Peripheral neuropathy
 Carpal tunnel syndrome
 Cranial neuropathy
 Guillain-Barre syndrome
 Chronic inflammatory demyelinating polyneuropathy
 Transverse myelitis
 Muscle disease


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