Intron retention in health and amyotrophic lateral sclerosis. [PDF]
Wang CY +8 more
europepmc +1 more source
Patient perspectives on transitioning to amyotrophic lateral sclerosis multidisciplinary clinics
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
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Muscle‐Specific Kinase Signaling and Its Therapeutic Potential
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]
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]
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
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Reachable Workspace as a Clinical Outcome for Upper Extremity Function: A Narrative Review
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]
Pan L +23 more
europepmc +1 more source
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
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]
Bhardwaj S +3 more
europepmc +1 more source

