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Obturator hernia associated with inclusion body myositis: a case report [PDF]

Journal of Medical Case Reports
Background Inclusion body myositis is a progressive muscle disease characterized by weakness, specifically in the flexor digitorum profundus and quadriceps muscles, and commonly affects men over 50 years of age.
Yuma Sato, Takashi Sugiyama, Kenjiro Uchino, Hitoshi Mochizuki   +3 more
doaj   +2 more sources

Electromyography varies by stage in inclusion body myositis [PDF]

Frontiers in Neurology, 2023
IntroductionInclusion body myositis (IBM) is a chronic inflammatory muscle disease that is characterized by mixed myogenic and neurogenic electromyography (EMG) findings.
Tomoo Mano, Tomoo Mano, Naohiko Iguchi, Nobuyuki Eura, Naoki Iwasa, Nanami Yamada, Hirosei Horikawa, Kazuma Sugie   +7 more
doaj   +2 more sources

Sporadic Inclusion Body Myositis: An Acquired Mitochondrial Disease with Extras

Biomolecules, 2019
The sporadic form of inclusion body myositis (IBM) is the most common late-onset myopathy. Its complex pathogenesis includes degenerative, inflammatory and mitochondrial aspects.
Boel De Paepe
doaj   +3 more sources

Ageing‐Associated Dysregulation of Myogenic Differentiation in Inclusion Body Myositis [PDF]

Journal of Cachexia, Sarcopenia and Muscle
Skeletal muscle is a postmitotic tissue dependent on a complex and tightly regulated regeneration process involving numerous intracellular and extracellular factors, including myogenic regulatory factors (MRFs), cytokines and myokines.
Geert M. deVries, Willem De Ridder, Jonathan Baets   +2 more
doaj   +2 more sources

Autoantibodies against a 43 KDa muscle protein in inclusion body myositis. [PDF]

PLoS ONE, 2011
BACKGROUND: Inclusion body myositis (IBM) is a poorly understood and refractory autoimmune muscle disease. Though widely believed to have no significant humoral autoimmunity, we sought to identify novel autoantibodies with high specificity for this ...
Mohammad Salajegheh, Theresa Lam, Steven A Greenberg   +2 more
doaj   +3 more sources

Proteomic profiles in inclusion body myositis and polymyositis with mitochondrial pathology [PDF]

Acta Neuropathologica Communications
Background Idiopathic inflammatory myopathies (IIMs) are autoimmune muscle diseases with distinct clinical, histopathological, and molecular features. Among them, inclusion body myositis (IBM) is refractory to immunotherapy and characterized by combined ...
Felix Kleefeld, Christina B. Schroeter, Donya Abdennebi, Vera Dobelmann, Sara Walli, Andreas Roos, Ute Distler, Stefan Tenzer, Tobias Bopp, Paula Quint, Linda-Isabell Schmitt, Markus Leo, Tim Hagenacker, Iago Pinal-Fernandez, Maria Casal-Dominguez, Andrew L. Mammen, Corinna Preuße, Lorenzo Maggi, Alexander Mensch, Sven G. Meuth, Werner Stenzel, Tobias Ruck, Christopher Nelke   +22 more
doaj   +2 more sources

Mitochondrial defects in sporadic inclusion body myositis—causes and consequences [PDF]

Frontiers in Cell and Developmental Biology
Sporadic inclusion body myositis (sIBM) is a distinct subcategory of Idiopathic Inflammatory Myopathies (IIM), characterized by unique pathological features such as muscle inflammation, rimmed vacuoles, and protein aggregation within the myofibers ...
Elsie Chit Yu Iu, Ho So, Chi Bun Chan
doaj   +2 more sources

Increasing daily duration of rehabilitation for inpatients with sporadic inclusion body myositis may contribute to improvement in activities of daily living: A nationwide database cohort study

Journal of Rehabilitation Medicine, 2023
Objective: To analyse the association between the daily duration of rehabilitation for inpatients with sporadic inclusion body myositis and improvement in activities of daily living, using a Japanese nationwide inpatient administrative claims database ...
Takuaki Tani, Shinobu Imai, Kiyohide Fushimi   +2 more
doaj   +1 more source

Clinical types of lung disease in polymyositis and dermatomyositis

Клинический разбор в общей медицине, 2021
The idiopathic inflammatory myopathies are a group of rare, heterogeneous connective tissue disorders characterized by skeletal muscle inflammation. The four main forms of idiopathic inflammatory myopathies are dermatomyositis, polymyositis, inclusion ...
Inna B. Bondarenko, Liubov A. Ponomareva, Elena N. Popova   +2 more
doaj   +1 more source

Inclusion body myositis in an older patient following a fall

Clinical Case Reports, 2023
Key Clinical Message After experiencing a fall, an 82‐year‐old woman developed progressive loss of lower limb strength and was diagnosed with inclusion body myositis.
Haruma Saiki, Hiroki Isono, Kousuke Ihara, Keisuke Kondo, Momoko Isono, Akira Shiraoka   +5 more
doaj   +1 more source