910
Views
109
CrossRef citations to date
0
Altmetric
SHORT REPORT

Proposed criteria for familial amyotrophic lateral sclerosis

, , , , , & show all
Pages 157-159 | Received 12 Aug 2010, Accepted 01 Dec 2010, Published online: 05 Jan 2011

References

  • Byrne S, Walsh C, Lynch C, Bede P, Elamin M, Kenna K, . Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis of the literature. J Neurol Neurosurg Psychiatry. (In press).
  • Valdmanis P, Rouleau G. Genetics of familial amyotrophic lateral sclerosis. Neurol. 2008;70: 144–52.
  • Giaggheddu M, Puggioni G, Masala C, Biancu F, Pirari G, Piras MR, . Epidemiological study of amyotrophic lateral sclerosis in Sardinia, Italy. Acta Neurol Scand. 1983;68:394–404.
  • Haverkamp LJ, Appel V, Appel SH. Natural history of amyotrophic lateral sclerosis in a database population: validation of a scoring system and a model for survival prediction. Brain. 1995;118:707–19.
  • Yeo L, Lynch C, Hardiman O. Validating population based registers for ALS: how accurate is death certification? J Neurol. 2010;257:1235–9.
  • Johnston CA, Stanton BR, Turner MR, Gray R, Hay-Ming Blunt A, Butt D, . Amyotrophic lateral sclerosis in an urban setting: a population based study of inner city London. J Neurol. 2006;252:1642–3.
  • Alonso A, Logroscino G, Jick S, Hernan MA. Incidence and lifetime risk of motor neuron disease in the United Kingdom: a population based study. Eur J Neurol. 2009;16: 745–51.
  • van Es AM, Dahlberg C, Birve A, Veldink JH, van den Berg LH, Andersen PM. Large-scale SOD1 mutation screening provides evidence for genetic heterogeneity in amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry. 2010;81:562–6.
  • Andersen PM, Nilsson P, Keranen ML, Forsgren L, Hagglund J, Karlsberg M. Phenotypic heterogeneity in motor neuron disease patients with Cu/Zn superoxidase dismutase mutations in Scandanavia. Brain. 1997;120: 1723–37.
  • Rabe M, Felbecker A, Waibel S, Steinbach P, Winter P, Ludolph AC. The epidemiology of Cu/Zn SOD mutations in Germany: a study of 217 families. J Neurol. 2010; 257:1298–1302.
  • Mackenzie IR, Rademakers R, Neumann M. TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia. Lancet Neurology. 2010;9:995–1007.
  • Vance C, Al-Chalabi A, Ruddy D, Smith B, Hu X, Sreedharan J, . Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13. 2–21.3. Brain. 2006;129:868–76.
  • Miller RG, Munsat TL, Swash M, Brooks BR. Consensus guidelines for the design and implementation of clinical trials in ALS. World Federation of Neurology committee on Research. J Neurol Sci. 1999;169:2–12.
  • Brooks BR. El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial ‘Clinical limits of amyotrophic lateral sclerosis’ workshop contributors. J Neurol Sci. 1994;124 (Suppl):96–107.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.