Results 221 to 230 of about 1,504,818 (288)

Quantitative Spatiotemporal Analysis of Ultrasound Images of Fasciculations in ALS

Muscle &Nerve, Volume 74, Issue 3, Page 644-655, September 2026.
ABSTRACT Introduction/Aims Fasciculations are a hallmark of amyotrophic lateral sclerosis (ALS), yet quantitative description of individual events on muscle ultrasound (MUS) is limited. We characterized the spatiotemporal kinematics of individual fasciculations to determine whether they differ between ALS and other neurogenic conditions.
Ryosuke Sugisawa, Kenji Sekiguchi, Yoshikatsu Noda, Shun Matoba, Hirotomo Suehiro, Jun Kozuki, Tomoko Tanaka, Norio Chihara   +7 more
wiley   +1 more source

Hypertrophic cardiomyopathy-linked Tnnc1 variants are associated with distinct myopathic changes in slow skeletal muscle of mice. [PDF]

J Muscle Res Cell Motil
Patel S, da Silva Santos GL, Florence J, Kahmini AR, Shi Y, Garcia MR, Gordon BS, Chase PB, Solís C, Laitano O, Pinto JR, Parvatiyar MS.   +11 more
europepmc   +1 more source

The Anterior Belly of the Digastric Muscle as a Novel Target for Needle Electromyography in Amyotrophic Lateral Sclerosis

Muscle &Nerve, Volume 74, Issue 3, Page 685-691, September 2026.
ABSTRACT Introduction/Aims Needle electromyography (EMG) in the bulbar region aids in the diagnosis of amyotrophic lateral sclerosis (ALS) but remains technically challenging. The genioglossus muscle (GM) is commonly examined; however, pain and poor relaxation may limit its evaluation.
Tatsuya Fukumoto, Yusuke Osaki, Kenta Hanada, Koji Fujita, Ryuji Kaji, Yuishin Izumi   +5 more
wiley   +1 more source

Sarcopenia, cachexia and frailty in older cats: Mechanisms, assessment and therapeutic considerations. [PDF]

J Feline Med Surg
Chandler M.
europepmc   +1 more source

With Regard to the Expression Status of Sarcolemmal Aquaporin 4 in Human Muscular Dystrophies

Neurology and Clinical Neuroscience, Volume 14, Issue 5, Page 354-361, September 2026.
ABSTRACT Human muscular dystrophies are inherited muscle‐wasting diseases caused by the various kinds of gene mutations. Among them, Duchenne muscular dystrophy (DMD) is a representative type. Before the discovery of the causative dystrophin gene of DMD, the fragile myofiber plasma membrane was thought to be the trigger of myofiber necrosis in DMD ...
Yoshihiro Wakayama, Takahiro Jimi
wiley   +1 more source

Three Adult Cases of ADHD With Comorbid Tic Symptoms Successfully Treated With Guanfacine Monotherapy

Neuropsychopharmacology Reports, Volume 46, Issue 3, September 2026.
Guanfacine extended‐release can be an effective monotherapy for adults with ADHD and comorbid tic disorders. A low dose of guanfacine was sufficient to produce a rapid improvement in tic symptoms in each patient before improving ADHD symptoms. ABSTRACT Tic disorders typically begin in childhood and often improve by adulthood, but some individuals ...
Koji Tada, Teruo Tada, Takashi Tsuboi, Koichiro Watanabe   +3 more
wiley   +1 more source

Effect of monochromatic light combinations on muscle fiber types in broilers after thyroidectomy. [PDF]

Poult Sci
Liu Y, Wang Z, Cao J, Dong Y, Gao T, Li F, Song E, Chen Y.   +7 more
europepmc   +1 more source

Plasma Lidocaine Concentrations During Intravenous Lidocaine Infusion Therapy in the Pediatric Population—A Scoping Review

Pediatric Anesthesia, Volume 36, Issue 9, Page 1041-1051, September 2026.
ABSTRACT Background Intravenous lidocaine therapy (IVLT) is often used in perioperative multimodal analgesia due to its analgesic, anti‐hyperalgesic, and anti‐inflammatory effects. In adults, IVLT doses of 1–2 mg/kg/h produce plasma concentrations of 1–2 μg/mL, within the presumed therapeutic range of 1–5 μg/mL.
McKenna Postles, Amanda Barton, Nicholas West, Gillian Lauder   +3 more
wiley   +1 more source

A randomized controlled trial of a health literacy-based digital intervention to promote postpartum recovery and self-care. [PDF]

Sci Rep
Wang Z, Li Q.
europepmc   +1 more source

Proteomic Profiling of Myofiber Repair Annexins and Their Role in Duchenne Muscular Dystrophy

PROTEOMICS, Volume 26, Issue 9, Page 6-23, September 2026.
ABSTRACT Myofiber regeneration and membrane repair play crucial roles in maintaining the continuous physiological functioning of the neuromuscular system. A swift and efficient repair mechanism enables the rapid restoration of sarcolemmal integrity following cellular impairment in damaged skeletal muscles.
Paul Dowling, Dounia Bouragba, Elisa Negroni, Capucine Trollet, Margit Zweyer, Dieter Swandulla, Kay Ohlendieck   +6 more
wiley   +1 more source