Results 171 to 180 of about 995,258 (307)

Intron retention in health and amyotrophic lateral sclerosis. [PDF]

open access: yesBrain
Wang CY   +8 more
europepmc   +1 more source

Patient perspectives on transitioning to amyotrophic lateral sclerosis multidisciplinary clinics

open access: yes, 2018
Kerri Lynn Schellenberg,1 Gregory Hansen2 1Department of Medicine, Division of Neurology, University of Saskatchewan, Saskatoon, SK, Canada; 2Department of Pediatrics, Division of Critical Care, University of Saskatchewan, Saskatoon, SK, Canada Purpose ...
Schellenberg KL, Hansen G
core  

Muscle‐Specific Kinase Signaling and Its Therapeutic Potential

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT The function of the neuromuscular junction (NMJ) is compromised in many neuromuscular diseases (NMDs) such as autoimmune or congenital myasthenia gravis (MG), amyotrophic lateral sclerosis (ALS), spinal muscular atrophy (SMA), and muscular dystrophies.
Stine Marie Jensen   +2 more
wiley   +1 more source

Cholesterol in amyotrophic lateral sclerosis: a bystander, a biomarker, or a target? [PDF]

open access: yesAtheroscler Plus
Farè M   +7 more
europepmc   +1 more source

What are the palliative care needs of people severely affected by neurodegenerative conditions, and how can a Specialist Palliative Care Service best meet these needs. [PDF]

open access: yes
Background: There is increasing recognition of the need for service development for patients in the advanced stages of neurological conditions. This study explores the palliative care needs of people with advanced amyotrophic lateral sclerosis ...
Veronese, Simone
core  

Reachable Workspace as a Clinical Outcome for Upper Extremity Function: A Narrative Review

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Motion sensing technology can be utilized to capture detailed upper extremity (UE) motion to reconstruct an individual's three‐dimensional (3D) reachable workspace (RWS). The RWS can be quantified as relative surface area (RSA), providing an innovative surrogate measure to assess UE mobility and function.
Jay J. Han   +3 more
wiley   +1 more source

Protein Biomarkers in Risk and Prognosis of Amyotrophic Lateral Sclerosis. [PDF]

open access: yesEur J Neurol
Pan L   +23 more
europepmc   +1 more source

Enabling Functional Independence: A Scoping Review of Upper Extremity Assistive Devices for Adults With Progressive Neuromuscular Diseases

open access: yesMuscle &Nerve, EarlyView.
This scoping review summarizes the spectrum of upper extremity assistive devices for adults with progressive neuromuscular diseases, ranging from low‐tech supports to advanced robotics, exoskeletons, and brain‐computer interface systems. While these technologies show promise for improving enabling function, current evidence is largely limited to ...
Katherine M. Burke   +13 more
wiley   +1 more source

Military Service and Survival Among Persons With ALS in the U.S. National ALS Registry, 2011–2023

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Introduction/Aims Military service has been associated with increased risk of amyotrophic lateral sclerosis (ALS) but less is known about survival after diagnosis. We evaluated the association between military service and survival after ALS diagnosis among U.S. National ALS Registry participants. Methods Participants who completed the Registry'
D. Kevin Horton   +5 more
wiley   +1 more source

Palliative Care Involvement in Hospitalized Amyotrophic Lateral Sclerosis Patients. [PDF]

open access: yesInt J Environ Res Public Health
Bhardwaj S   +3 more
europepmc   +1 more source

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