[HTML][HTML] A comprehensive review of amyotrophic lateral sclerosis
S Zarei, K Carr, L Reiley, K Diaz, O Guerra… - Surgical neurology …, 2015 - ncbi.nlm.nih.gov
Amyotrophic lateral sclerosis (ALS) is a late-onset fatal neurodegenerative disease affecting
motor neurons with an incidence of about 1/100,000. Most ALS cases are sporadic, but 5 …
motor neurons with an incidence of about 1/100,000. Most ALS cases are sporadic, but 5 …
Amyotrophic lateral sclerosis
JD Mitchell, GD Borasio - The lancet, 2007 - thelancet.com
Amyotrophic lateral sclerosis (known in the UK as motor neuron disease) is a devastating
illness with uncertain pathogenesis. In this Seminar, we review its natural history, clinical …
illness with uncertain pathogenesis. In this Seminar, we review its natural history, clinical …
A brain-computer interface for long-term independent home use
EW Sellers, TM Vaughan… - Amyotrophic lateral …, 2010 - Taylor & Francis
Our objective was to develop and validate a new brain-computer interface (BCI) system
suitable for long-term independent home use by people with severe motor disabilities. The …
suitable for long-term independent home use by people with severe motor disabilities. The …
End-of-life management in patients with amyotrophic lateral sclerosis
Most health-care professionals are trained to promote and maintain life and often have
difficulty when faced with the often rapid decline and death of people with terminal illnesses …
difficulty when faced with the often rapid decline and death of people with terminal illnesses …
Diagnosis and treatment of bulbar symptoms in amyotrophic lateral sclerosis
P Kühnlein, HJ Gdynia, AD Sperfeld… - Nature clinical practice …, 2008 - nature.com
Amyotrophic lateral sclerosis (ALS) is the most common neurodegenerative disease of the
motor system. Bulbar symptoms such as dysphagia and dysarthria are frequent features of …
motor system. Bulbar symptoms such as dysphagia and dysarthria are frequent features of …
Depression and anxiety in individuals with amyotrophic lateral sclerosis: epidemiology and management
Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease with no curative
treatment. Considering the devastating nature of the disease, a high prevalence of …
treatment. Considering the devastating nature of the disease, a high prevalence of …
[HTML][HTML] Respiratory muscle training in neuromuscular disease: a systematic review and meta-analysis
Background Neuromuscular disease causes a progressive decline in ventilatory function
which respiratory muscle training may address. Previous systematic reviews have focussed …
which respiratory muscle training may address. Previous systematic reviews have focussed …
Speech deterioration in amyotrophic lateral sclerosis (ALS) after manifestation of bulbar symptoms
T Makkonen, H Ruottinen, R Puhto… - … journal of language …, 2018 - Wiley Online Library
Background The symptoms and their progression in amyotrophic lateral sclerosis (ALS) are
typically studied after the diagnosis has been confirmed. However, many people with ALS …
typically studied after the diagnosis has been confirmed. However, many people with ALS …
Changing trends in the management of end-stage neuromuscular respiratory muscle failure: recommendations of an international consensus
JR Bach, MR Gonçalves, A Hon… - American Journal of …, 2013 - journals.lww.com
Objective Respiratory management of patients with end-stage respiratory muscle failure of
neuromuscular disease has evolved from no treatment and inevitable respiratory failure to …
neuromuscular disease has evolved from no treatment and inevitable respiratory failure to …
Psychological wellbeing and quality of life in amyotrophic lateral sclerosis: a review
F Pagnini - International Journal of Psychology, 2013 - Taylor & Francis
Amyotrophic lateral sclerosis is a fatal neurodegenerative disease with a progressive and
rapid course that, so far, cannot be stopped or reversed. The psychological impact of the …
rapid course that, so far, cannot be stopped or reversed. The psychological impact of the …