Amyotrophic lateral sclerosis: pathophysiology, diagnosis and management
PH Gordon - CNS drugs, 2011 - Springer
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease associated
with a life expectancy of approximately 3 years after symptom onset, but the range of survival …
with a life expectancy of approximately 3 years after symptom onset, but the range of survival …
Outcomes research in amyotrophic lateral sclerosis: lessons learned from the amyotrophic lateral sclerosis clinical assessment, research, and education database
RG Miller, F Anderson, BR Brooks… - Annals of …, 2009 - Wiley Online Library
Objective To examine the care of patients with ALS following the publication of the
standardized recommendations for the management of patients with amyotrophic lateral …
standardized recommendations for the management of patients with amyotrophic lateral …
Profile of patients with amyotrophic lateral sclerosis across continuum of care
V Kehyayan, L Korngut, N Jetté… - Canadian Journal of …, 2014 - cambridge.org
Objective: This study describes the socio-demographic and clinical profile of persons with
amyotrophic lateral sclerosis (ALS) in home care, nursing homes and complex continuing …
amyotrophic lateral sclerosis (ALS) in home care, nursing homes and complex continuing …
Current potential therapeutics of amyotrophic lateral sclerosis
L Lu, Y Deng, R Xu - Frontiers in Neurology, 2024 - frontiersin.org
Amyotrophic lateral sclerosis (ALS) is a debilitating motor neurological disorder for which
there is still no cure. The disease seriously jeopardizes the health and lifespan of adult …
there is still no cure. The disease seriously jeopardizes the health and lifespan of adult …
Prognostic factors for survival in patients with amyotrophic lateral sclerosis: analysis of a multi-centre clinical trial
E Yates, MK Rafiq - Journal of Clinical Neuroscience, 2016 - Elsevier
Abstract Information regarding factors influencing prognosis and quality of life (QoL) in
patients with amyotrophic lateral sclerosis (ALS) is useful for clinicians and also for patients …
patients with amyotrophic lateral sclerosis (ALS) is useful for clinicians and also for patients …
Time for optimism in amyotrophic lateral sclerosis
P Corcia, C Lunetta, P Vourc'h… - European Journal of …, 2023 - Wiley Online Library
Background and purpose Amyotrophic lateral sclerosis (ALS) is among the most common
motor neuron diseases in adults. Nevertheless, ALS remains fatal, despite decades of …
motor neuron diseases in adults. Nevertheless, ALS remains fatal, despite decades of …
Symptomatic therapy and palliative aspects of clinical care
PH Gordon, H Mitsumoto - Handbook of clinical neurology, 2007 - Elsevier
Publisher Summary This chapter presents the diagnosis to patients, treating various
symptoms, and discusses the timing and institution of palliative care in amyotrophic lateral …
symptoms, and discusses the timing and institution of palliative care in amyotrophic lateral …
Clinical diagnosis and management of amyotrophic lateral sclerosis
O Hardiman, LH Van Den Berg… - Nature reviews neurology, 2011 - nature.com
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that results in
progressive loss of bulbar and limb function. Patients typically die from respiratory failure …
progressive loss of bulbar and limb function. Patients typically die from respiratory failure …
The clinical features and prognosis of amyotrophic lateral sclerosis
H Mitsumoto - Amyotrophic lateral sclerosis: A guide for patients …, 2009 - books.google.com
The human brain has billions of nerve cells, or neurons. There are more than 80 different
types of these nerve cells, and some are highly specialized. Diseases that cause neuron …
types of these nerve cells, and some are highly specialized. Diseases that cause neuron …