Clinical and genetic basis of familial amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis represents the most common neurodegenerative disease leading to upper and lower motor neuron compromise. Although the vast majority of cases are sporadic, substantial gain has been observed in the knowledge of the genetic forms of the disease, especially of familial for...
Main Authors: | Paulo Victor Sgobbi de Souza, Wladimir Bocca Vieira de Rezende Pinto, Marco Antônio Troccoli Chieia, Acary Souza Bulle Oliveira |
---|---|
Format: | Article |
Language: | English |
Published: |
Academia Brasileira de Neurologia (ABNEURO)
2015-01-01
|
Series: | Arquivos de Neuro-Psiquiatria |
Subjects: | |
Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2015005050161&lng=en&tlng=en |
Similar Items
-
Mortality rates due to amyotrophic lateral sclerosis in São Paulo City from 2002 to 2006
by: Sheila Evangelista de Matos, et al.
Published: (2011-12-01) -
Impacto do tratamento medicamentoso na voz, fala e deglutição de pacientes com esclerose lateral amiotrófica: revisão sistemática
by: Keila Maruze de França Albuquerque, et al.
Published: (2022-05-01) -
Current issues in the respiratory care of patients with amyotrophic lateral sclerosis
by: Marco Orsini, et al.
Published: (2015-10-01) -
Amyotrophic lateral sclerosis: considerations on diagnostic criteria
by: Marco A. Chieia, et al.
Published: (2010-12-01) -
A clinical epidemiological study of 251 cases of amyotrophic lateral sclerosis in the south of Brazil Estudo clínico epidemiológico de 251 casos de esclerose lateral amiotrófica no sul do Brasil
by: Lineu Cesar Werneck, et al.
Published: (2007-06-01)