Results 231 to 240 of about 176,773 (340)

Pharmacological Treatment of Dysphagia in Stroke [PDF]

open access: bronze, 1997
David Smithard   +2 more
openalex   +1 more source

Food—Consistency/Texture—Specific Pharyngeal Dystonia: A Novel Form of Focal Task‐Specific Dystonia

open access: yes
Movement Disorders Clinical Practice, EarlyView.
Domenico A. Restivo   +5 more
wiley   +1 more source

A Phase 1, Double‐Blind, Placebo‐Controlled Trial of Sevasemten (EDG‐5506), a Selective Modulator of Fast Skeletal Muscle Contraction, in Healthy Volunteers and Adults With Becker Muscular Dystrophy

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Introduction/Aims Sevasemten (EDG‐5506) is an orally administered, investigational small molecule that selectively modulates fast muscle fiber contraction by inhibiting fast myosin ATPase. This study assessed the safety, tolerability, and pharmacokinetics (PK)/pharmacodynamics (PD) of sevasemten in healthy adult volunteers (HVs) and adults ...
Joanne Donovan   +11 more
wiley   +1 more source

Efficacy and Safety of Once Daily Dosing vs. Approved On/Off Dosing of Edaravone Oral Suspension Up to 48 Weeks in Patients With Amyotrophic Lateral Sclerosis (Study MT‐1186‐A02)

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Introduction/Aims An On/Off dosing regimen of intravenous (IV) edaravone and edaravone oral suspension is approved in the US for the treatment of amyotrophic lateral sclerosis (ALS). Placebo‐controlled clinical trials showed IV edaravone slows the rate of physical functional decline.
Jeffrey Rothstein   +17 more
wiley   +1 more source

Dysphagia After Pediatric Laryngotracheal Reconstruction-A Scoping Review. [PDF]

open access: yesLaryngoscope Investig Otolaryngol
Singh N   +3 more
europepmc   +1 more source

Safety Extension Study of Edaravone Oral Suspension in Patients With Amyotrophic Lateral Sclerosis for up to an Additional 96 Weeks of Treatment

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Introduction/Aims Edaravone intravenous (IV) and oral suspension have been shown to have similar pharmacokinetics, safety, and slowing of functional decline in patients with amyotrophic lateral sclerosis (ALS). Study MT‐1186‐A01 indicated that edaravone oral suspension was well‐tolerated over 48 weeks, with no new safety concerns identified ...
Angela Genge   +17 more
wiley   +1 more source

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