Amyotrophic lateral sclerosis type 8 is not a pure motor disease: evidence from a neuropsychological and behavioural study
Author:
Funder
FAPEMIG
CNPQ
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
http://link.springer.com/content/pdf/10.1007/s00415-019-09369-y.pdf
Reference40 articles.
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2. Nijssen J, Comley LH, Hedlund E (2017) Motor neuron vulnerability and resistance in amyotrophic lateral sclerosis. Acta Neuropathol 133:863–885
3. Alsultan AA, Waller R, Heath PR, Kirby J (2016) The genetics of amyotrophic lateral sclerosis: current insights. Degener Neurol Neuromuscul Dis 6:49–64
4. Nishimura AL, Mitne-Neto M, Silva HCA, Richieri-Costa A, Middleton S, Cascio D et al (2004) A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis. Am J Hum Genet 75:822–831
5. Richieri-Costa A, Rogatko A, Levisky R, Finkel N, Frota-Pessoa O (1981) Autossomal dominant late adult spinal muscular atrophy, type Finkel. Am J Med Genet 9(2):119–128
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