Results 81 to 90 of about 19,247 (225)
Muscle &Nerve, Volume 73, Issue 3, Page 485-489, March 2026.ABSTRACT Introduction/Aims Dissociation of echogenicity of the flexor digitorum profundus (FDP) and flexor carpi ulnaris (FCU) on neuromuscular ultrasound has been reported to be a useful sign to differentiate inclusion body myositis (IBM) from more common disease mimics, but it is not clear that this finding is pathognomonic of IBM. Our study aimed to
Anson W. Wilks, Nizar Chahin
wiley +1 more source
Rare manifestation of a c.290 C\u3eT, p.Gly97Glu VCP mutation [PDF]
, 2015 Introduction. The valosin-containing protein (VCP) regulates several distinct cellular processes. Consistent with this, VCP mutations manifest variable clinical phenotypes among and within families and are a diagnostic challenge. Methods.
Chou, Tsui-Fen +9 more
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NMR in Biomedicine, Volume 39, Issue 3, March 2026.We evaluated the random permeable barrier model (RPBM) through simulations, model fitting, and in vivo analysis of 100 healthy adults. Simulations showed that stable estimates of muscle cell diameter and membrane permeability require constraining τ and fixing D0 at ~0.9 of axial diffusivity at long diffusion times.
Martijn Froeling +4 more
wiley +1 more source
Cardiac involvement in the dystrophinopathies
Journal of Pediatric Rehabilitation Medicine, 2008 The dystrophinopathies are a group of disorders that are characterized by absence or deficiency of functional dystrophin, a large cytoskeletal protein of striated muscle that is closely associated with transmembrane glycoprotein complexes.
Mark W. Russell +2 more
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Adult patient with Becker dystrophy undergoing orthopedic surgery: an anesthesia challenge
International Medical Case Reports Journal, 2018 Masoud Parish, Haleh Farzin Anesthesiology Department, Tabriz University of Medical Sciences, Shohada Teaching Hospital, Tabriz, Iran Abstract: Muscular dystrophies are considered to be a series of neuromuscular diseases with genetic causes and are ...
Parish M, Farzin H
doaj
Arquivos de Neuro-Psiquiatria, 1995 The dystrophin distribution in the plasma muscle membrane using immunohystochemistry was studied in 22 children with congenital muscular dystrophy. The dystrophin was detected by immunofluorescence in muscle biopsy through a polyclonal antibody.
Lineu Cesar Werneck, Eduardo Bonilla
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Metabolic Alterations in Cardiomyocytes of Patients with Duchenne and Becker Muscular Dystrophies [PDF]
, 2019 Duchenne and Becker muscular dystrophies (DMD/BMD) result in progressive weakness of skeletal and cardiac muscles due to the deficiency of functional dystrophin.
Carsana, Antonella, Esposito, Gabriella
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Frontiers in Neurology, 2019 Background: The inclusion of resistance training in the treatment and management of muscular dystrophy has previously been discouraged, based on mainly anecdotal evidence.
Emma L. Bostock +6 more
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N-terminal α Dystroglycan (αDG-N): A Potential Serum Biomarker for Duchenne Muscular Dystrophy [PDF]
, 2018 Biological Sciences: 2nd Place (The Ohio State University Edward F. Hayes Graduate Research Forum)Background: Duchenne Muscular Dystrophy (DMD) is a severe, progressive, neuromuscular disorder of childhood.
Crowe, Kelly E.
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Muscular dystrophies: key elements for everyday diagnosis and management
Cardiogenetics, 2013 Muscular dystrophies are a heterogeneous group of inherited disorders that share similar clinical features and dystrophic changes on muscle biopsy, associated with progressive weakness. Weakness may be noted at birth or develop in late adult life.
Alberto Palladino +2 more
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