Results 101 to 110 of about 2,106 (149)

Sporadic Inclusion Body Myositis Presenting with Beevor's Sign

Internal Medicine, 2015
Sugie, Kazuma, Kumazawa, Aya, Ueno, Satoshi   +2 more
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Concomitant occurrence of FXTAS and clinically defined sporadic inclusion body myositis: report of two cases. [PDF]

Croat Med J, 2017
Lechpammer M, Martínez Cerdeńo V, Hunsaker MR, Hah M, Gonzales H, Tisch S, Joffe R, Pamphlett R, Tassone F, Hagerman PJ, Bolitho SJ, Hagerman RJ.   +11 more
europepmc   +1 more source

Calcium dysregulation, functional calpainopathy, and endoplasmic reticulum stress in sporadic inclusion body myositis. [PDF]

Acta Neuropathol Commun, 2017
Amici DR, Pinal-Fernandez I, Mázala DA, Lloyd TE, Corse AM, Christopher-Stine L, Mammen AL, Chin ER.   +7 more
europepmc   +1 more source

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Sporadic Inclusion Body Myositis

Neurology India, 2021
Background: Sporadic inclusion body myositis (s-IBM) is rare in India. Aim: The aim of this study was to diagnose s-IBM according to the European Neuromuscular Center (ENMC) IBM research diagnostic criteria 2011. Materials and Methods: A
Sundaram, Challa, Saumya, Jakati, Swethalakshmi, Narla, Megha S, Uppin, Meena A, Kannan, M K Murthy, Jagarlapudi   +5 more
openaire   +2 more sources

Epidemiology of sporadic inclusion body myositis

Current Opinion in Rheumatology, 2016
Purpose of review In this review, we describe recent progress in the clinical epidemiology of sporadic inclusion body myositis (IBM). Recent findings In a population-based, retrospective study from Norway, performed with a denominator population of 2.6 million; and with cases ...
Øyvind, Molberg, Cecilie, Dobloug
openaire   +2 more sources

Follistatin Gene Therapy for Sporadic Inclusion Body Myositis Improves Functional Outcomes [PDF]

Molecular Therapy, 2017
Mehmet Yalvac, Kevin Flanigan, Natalie Reash   +2 more
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Interstitial amyloidosis in sporadic inclusion body myositis

Muscle & Nerve, 2021
AbstractIntroduction/AimsIntracellular congophilic inclusions within muscle fibers, although nonspecific, are one of the pathological hallmarks of sporadic inclusion body myositis (sIBM). Extracellular amyloid deposits in muscle, on the other hand, are the canonical findings of amyloid myopathies, which occur with or without systemic amyloidosis ...
Mazen Alamr, Margherita Milone, Elie Naddaf, Steven R. Ytterberg, Stephanie J. Steel, Lyell K. Jones, Teerin Liewluck   +6 more
openaire   +2 more sources

Sporadic Inclusion Body Myositis

Brain and nerve = Shinkei kenkyu no shinpo
Sporadic inclusion body myositis (sIBM) is an intractable and progressive skeletal muscle disease of unknown etiology. Muscle biopsy typically reveals endomysial inflammation, invasion of mononuclear cells into non-necrotic fibers, and rimmed vacuoles, suggesting that inflammation and degeneration co-exist in the pathomechanism.
Albert Selva-O’Callaghan, Ana Matas-Garcia, Jose Milisenda   +2 more
openaire   +3 more sources

Sporadic Inclusion Body Myositis and Hereditary Inclusion Body Myopathy

Journal of Clinical Neuromuscular Disease, 2002
Sporadic inclusion body myositis (s-IBM) is a common but under-recognized myopathy in individuals over 50 years of age. An awareness of the clinical phenotype and of the electrodiagnostic and histopathologic features should lead to improved recognition, and should minimize confusion with polymyositis, motor neuron disease, and other neuromuscular ...
Zachary, Simmons, Javad, Towfighi
openaire   +2 more sources