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Clinical

Twelve-month duration as an appropriate criterion for flail arm syndrome

, &
Pages 29-33 | Received 02 Jun 2019, Accepted 28 Aug 2019, Published online: 16 Sep 2019

References

  • Chio A, Logroscino G, Hardiman O, Swingler R, Mitchell D, Beghi E, et al. Prognostic factors in ALS: a critical review. Amyotroph Lateral Scler. 2009;10:310–23.
  • Robberecht W, Philips T. The changing scene of amyotrophic lateral sclerosis. Nat Rev Neurosci. 2013;14:248–64.
  • Mandrioli J, Faglioni P, Nichelli P, Sola P. Amyotrophic lateral sclerosis: prognostic indicators of survival. Amyotroph Lateral Scler. 2006;7:217–20.
  • Wijesekera LC, Mathers S, Talman P, Galtrey C, Parkinson MH, Ganesalingam J, et al. Natural history and clinical features of the flail arm and flail leg ALS variants. Neurology. 2009;72:1087–94.
  • Yoon BN, Choi SH, Rha JH, Kang SY, Lee KW, Sung JJ. Comparison between flail arm syndrome and upper limb onset amyotrophic lateral sclerosis: clinical features and electromyographic findings. Exp Neurobiol. 2014;23:253–7.
  • Chio A, Calvo A, Moglia C, Mazzini L, Mora G, PARALS Study Group. Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study. J Neurol Neurosurg Psychiatry. 2011;82:740–6.
  • Hino S, Sasaki S. Flail arm syndrome with cytoplasmic vacuoles in remaining anterior horn motor neurons: a peculiar variant of amyotrophic lateral sclerosis. Neuropathology. 2015;35:582–6.
  • Gamez J, Cervera C. Brachial amyotrophic diplegia: a slowly progressive motor neuron disorder. Neurology. 2000;54:2355.
  • Gamez J, Cervera C, Codina A. Flail arm syndrome of Vulpian-Bernhart's form of amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry. 1999;67:258.
  • Hu MT, Ellis CM, Al-Chalabi A, Leigh PN, Shaw CE. Flail arm syndrome: a distinctive variant of amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry. 1998;65:950–1.
  • Al-Chalabi A, Hardiman O, Kiernan MC, Chio A, Rix-Brooks B, van den Berg LH. Amyotrophic lateral sclerosis: moving towards a new classification system. Lancet Neurol. 2016;15:1182–94.
  • Hubers A, Hildebrandt V, Petri S, Kollewe K, Hermann A, Storch A, et al. Clinical features and differential diagnosis of flail arm syndrome. J Neurol. 2016;263:390–5.
  • Chen L, Zhang B, Chen R, Tang L, Liu R, Yang Y, et al. Natural history and clinical features of sporadic amyotrophic lateral sclerosis in China. J Neurol Neurosurg Psychiatry. 2015;86:1075–81.
  • Vucic S, Kiernan MC. Abnormalities in cortical and peripheral excitability in flail arm variant amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry. 2007;78:849–52.
  • Yang H, Liu M, Li X, Cui B, Fang J, Cui L. Neurophysiological differences between flail arm syndrome and amyotrophic lateral sclerosis. PLOS One. 2015;10:e0127601.
  • Brooks BR, Miller RG, Swash M, Munsat TL. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000;1:293–9.
  • Chen L, Liu X, Tang L, Zhang N, Fan D. Long-term use of riluzole could improve the prognosis of sporadic amyotrophic lateral sclerosis patients: a real-world cohort study in China. Front Aging Neurosci. 2016;8:246.
  • Zoccolella S, Beghi E, Palagano G, Fraddosio A, Guerra V, Samarelli V, et al. Analysis of survival and prognostic factors in amyotrophic lateral sclerosis: a population based study. J Neurol Neurosurg Psychiatry. 2008;79:33–7.
  • Liu X, He J, Gao FB, Gitler AD, Fan D. The epidemiology and genetics of amyotrophic lateral sclerosis in China. Brain Res. 2018;1693:121–6.

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