Similar articles for PMID: 19506136

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1

Defining survival as an outcome measure in amyotrophic lateral sclerosis.

Gordon PH, Corcia P, Lacomblez L, Pochigaeva K, Abitbol JL, Cudkowicz M, Leigh PN, Meininger V. Gordon PH, et al. Arch Neurol. 2009 Jun;66(6):758-61. doi: 10.1001/archneurol.2009.1. Arch Neurol. 2009. PMID: 19506136

2

Efficacy and safety of xaliproden in amyotrophic lateral sclerosis: results of two phase III trials.

Meininger V, Bensimon G, Bradley WR, Brooks B, Douillet P, Eisen AA, Lacomblez L, Leigh PN, Robberecht W. Meininger V, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2004 Jun;5(2):107-17. doi: 10.1080/14660820410019602. Amyotroph Lateral Scler Other Motor Neuron Disord. 2004. PMID: 15204012 Clinical Trial.

3

[The changes of clinical characteristics in 100 Japanese amyotrophic lateral sclerosis patients between 1980 and 2000].

Kimura F, Shinoda K, Fujiwara S, Fujimura C, Nakajima H, Furutama D, Sugino M, Hanafusa T. Kimura F, et al. Rinsho Shinkeigaku. 2003 Jul;43(7):385-91. Rinsho Shinkeigaku. 2003. PMID: 14582363 Japanese.

4

Respiratory systems abnormalities and clinical milestones for patients with amyotrophic lateral sclerosis with emphasis upon survival.

Vender RL, Mauger D, Walsh S, Alam S, Simmons Z. Vender RL, et al. Amyotroph Lateral Scler. 2007 Feb;8(1):36-41. doi: 10.1080/17482960600863951. Amyotroph Lateral Scler. 2007. PMID: 17364434

5

Survival and quality of life after tracheostomy for acute respiratory failure in patients with amyotrophic lateral sclerosis.

Vianello A, Arcaro G, Palmieri A, Ermani M, Braccioni F, Gallan F, Soraru' G, Pegoraro E. Vianello A, et al. J Crit Care. 2011 Jun;26(3):329.e7-14. doi: 10.1016/j.jcrc.2010.06.003. Epub 2010 Jul 23. J Crit Care. 2011. PMID: 20655697

6

Outcome and attitudes toward home tracheostomy ventilation of consecutive patients: a 10-year experience.

Marchese S, Lo Coco D, Lo Coco A. Marchese S, et al. Respir Med. 2008 Mar;102(3):430-6. doi: 10.1016/j.rmed.2007.10.006. Epub 2007 Nov 19. Respir Med. 2008. PMID: 18023334 Free article.

7

[Clinical characteristics of elderly Japanese patients with amyotrophic lateral sclerosis; with special reference to the development of respiratory failure].

Terao S, Miura N, Osano Y, Adachi K, Sobue G. Terao S, et al. Rinsho Shinkeigaku. 2006 Jun;46(6):381-9. Rinsho Shinkeigaku. 2006. PMID: 16986698 Japanese.

8

Can selection of rapidly progressing patients shorten clinical trials in amyotrophic lateral sclerosis?

de Carvalho M, Swash M. de Carvalho M, et al. Arch Neurol. 2006 Apr;63(4):557-60. doi: 10.1001/archneur.63.4.557. Arch Neurol. 2006. PMID: 16606769

9

The ALSFRSr predicts survival time in an ALS clinic population.

Kaufmann P, Levy G, Thompson JL, Delbene ML, Battista V, Gordon PH, Rowland LP, Levin B, Mitsumoto H. Kaufmann P, et al. Neurology. 2005 Jan 11;64(1):38-43. doi: 10.1212/01.WNL.0000148648.38313.64. Neurology. 2005. PMID: 15642901

10

[Revised amyotrophic lateral sclerosis functional rating scale at time of diagnosis predicts survival time in amyotrophic lateral sclerosis].

Liu XX, Fan DS, Zhang J, Zhang S, Zheng JY. Liu XX, et al. Zhonghua Yi Xue Za Zhi. 2009 Sep 22;89(35):2472-5. Zhonghua Yi Xue Za Zhi. 2009. PMID: 20137433 Chinese.

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