EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)–revised report of an EFNS task force
EFNS Task Force on Diagnosis and … - European journal of …, 2012 - Wiley Online Library
Background: The evidence base for the diagnosis and management of amyotrophic lateral
sclerosis (ALS) is weak. Objectives: To provide evidence‐based or expert recommendations …
sclerosis (ALS) is weak. Objectives: To provide evidence‐based or expert recommendations …
Supportive and symptomatic management of amyotrophic lateral sclerosis
EV Hobson, CJ McDermott - Nature Reviews Neurology, 2016 - nature.com
The main aims in the care of individuals with amyotrophic lateral sclerosis (ALS) are to
minimize morbidity and maximize quality of life. Although no cure exists for ALS, supportive …
minimize morbidity and maximize quality of life. Although no cure exists for ALS, supportive …
Pain in amyotrophic lateral sclerosis
Pain is a largely neglected symptom in patients with amyotrophic lateral sclerosis (ALS)
although it is reported by most of these patients. It occurs at all stages of the disease and can …
although it is reported by most of these patients. It occurs at all stages of the disease and can …
Polyanalgesic Consensus Conference 2012: recommendations for the management of pain by intrathecal (intraspinal) drug delivery: report of an interdisciplinary …
TR Deer, J Prager, R Levy, J Rathmell… - … : Technology at the …, 2012 - Elsevier
Introduction The use of intrathecal (IT) infusion of analgesic medications to treat patients with
chronic refractory pain has increased since its inception in the 1980s, and the need for …
chronic refractory pain has increased since its inception in the 1980s, and the need for …
Canadian best practice recommendations for the management of amyotrophic lateral sclerosis
C Shoesmith, A Abrahao, T Benstead, M Chum… - Cmaj, 2020 - Can Med Assoc
The care and management of patients with ALS should always be patient focused, with
attention to holistic and emotional aspects of well-being. It is the patient who ultimately …
attention to holistic and emotional aspects of well-being. It is the patient who ultimately …
A systematic review of non-motor symptom evaluation in clinical trials for amyotrophic lateral sclerosis
Background Amyotrophic lateral sclerosis (ALS) is increasingly recognised as a multi-
system disorder, presenting with common and impactful non-motor symptoms, such as …
system disorder, presenting with common and impactful non-motor symptoms, such as …
Care management in amyotrophic lateral sclerosis
MH Soriani, C Desnuelle - Revue neurologique, 2017 - Elsevier
Amyotrophic lateral sclerosis (ALS) is a relentlessly progressive and fatal
neurodegenerative disease characterized by progressive weakness of voluntary muscles of …
neurodegenerative disease characterized by progressive weakness of voluntary muscles of …
Pain in neurodegenerative disease: current knowledge and future perspectives
Neurodegenerative diseases are going to increase as the life expectancy is getting longer.
The management of neurodegenerative diseases such as Alzheimer's disease (AD) and …
The management of neurodegenerative diseases such as Alzheimer's disease (AD) and …
Amyotrophic lateral sclerosis and palliative care: where we are, and the road ahead
LJ Blackhall - Muscle & nerve, 2012 - Wiley Online Library
Patients with amyotrophic lateral sclerosis (ALS) have high symptom burdens, including
pain, fatigue, dyspnea, and sialorrhea, and they must make difficult decisions about the use …
pain, fatigue, dyspnea, and sialorrhea, and they must make difficult decisions about the use …
Nonmotor symptoms in amyotrophic lateral sclerosis: a systematic review
Background: ALS is a progressive neurodegenerative disease with no curative treatment.
Nonmotor symptoms presenting in ALS may cause significant distress, worsen prognosis …
Nonmotor symptoms presenting in ALS may cause significant distress, worsen prognosis …