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Neurology
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Amyotrophic lateral sclerosis

Citations 1-10 of 223 total displayed.

Most recent content (17 Nov 2009):

ARTICLES
Lower serum lipid levels are related to respiratory impairment in patients with ALS
A. Chiò, A. Calvo, A. Ilardi, E. Cavallo, C. Moglia, R. Mutani, A. Palmo, R. Galletti, K. Marinou, L. Papetti, and G. Mora
Neurology 2009; 73: 1681-1685. [Abstract] [Full text] [PDF]  

ARTICLES
Study of 962 patients indicates progressive muscular atrophy is a form of ALS
W. -K. Kim, X. Liu, J. Sandner, M. Pasmantier, J. Andrews, L. P. Rowland, and H. Mitsumoto
Neurology 2009; 73: 1686-1692. [Abstract] [Full text] [PDF]  

VIEWS AND REVIEWS
Smoking may be considered an established risk factor for sporadic ALS
Carmel Armon
Neurology 2009; 73: 1693-1698. [Abstract] [Full text] [PDF]  

Past content (since Jan 2001):

EDITORIALS
Another gene for ALS: Mutations in sporadic cases and the rare variant hypothesis
Kevin Talbot
Neurology 2009; 73: 1172-1173. [Full text] [PDF]  

ARTICLES
Mutations in FUS cause FALS and SALS in French and French Canadian populations
V. V. Belzil, P. N. Valdmanis, P. A. Dion, H. Daoud, E. Kabashi, A. Noreau, J. Gauthier, for the S2D team, P. Hince, A. Desjarlais, J. -P. Bouchard, L. Lacomblez, F. Salachas, P. -F. Pradat, W. Camu, V. Meininger, N. Dupré, and G. A. Rouleau
Neurology 2009; 73: 1176-1179. [Abstract] [Full text] [PDF]  

ARTICLES
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
N. Ticozzi, V. Silani, A. L. LeClerc, P. Keagle, C. Gellera, A. Ratti, F. Taroni, T. J. Kwiatkowski, Jr, D. M. McKenna-Yasek, P. C. Sapp, R. H. Brown, Jr, and J. E. Landers
Neurology 2009; 73: 1180-1185. [Abstract] [Full text] [PDF]  

ARTICLES
Trends and determinants of end-of-life practices in ALS in the Netherlands
M. Maessen, J. H. Veldink, B. D. Onwuteaka-Philipsen, J. M. de Vries, J.H.J. Wokke, G. van der Wal, and L. H. van den Berg
Neurology 2009; 73: 954-961. [Abstract] [Full text] [PDF]  

EDITORIALS
Another gene for ALS. Mutations in sporadic cases and the rare variant hypothesis
Kevin Talbot
Neurology first published on September 9, 2009 as doi: WNL.0b013e3181bd1161. Rapid PDF  

ARTICLES
Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort
N. Ticozzi, V. Silani, A. L. LeClerc, P. Keagle, C. Gellera, A. Ratti, F. Taroni, T. J. Kwiatkowski, Jr., D. M. McKenna-Yasek, P. C. Sapp, R. H. Brown, Jr., and J. E. Landers
Neurology first published on September 9, 2009 as doi: WNL.0b013e3181bbff05. [Abstract] Rapid PDF  

ARTICLES
Mutations in FUS cause FALS and SALS in French and French Canadian populations
V. V. Belzil, P. N. Valdmanis, P. A. Dion, H. Daoud, E. Kabashi, A. Noreau, J. Gauthier, for the S2D team, P. Hince, A. Desjarlais, J.-P. Bouchard, L. Lacomblez, F. Salachas, P.-F. Pradat, W. Camu, V. Meininger, N. Dupré, and G. A. Rouleau
Neurology first published on September 9, 2009 as doi: WNL.0b013e3181bbfeef. [Abstract] Rapid PDF  

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* 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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