Results 101 to 110 of about 9,601 (224)
International Journal of Physiotherapy, 2017 Background: Sporadic inclusion body myositis is an autoimmune and degenerative disorder of skeletal muscle that affects people at random. It most commonly begins as progressive weakness and atrophy of lower extremity musculature, beginning with the ...
Tyler Harrigfeld, Trent Jackman
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Sonography, Volume 13, Issue 3, September 2026.ABSTRACT Objective This study aimed to develop and validate an ultrasound‐based model integrating conventional ultrasound and calcification patterns (US‐CAL) for distinguishing benign from malignant calcified soft tissue masses. Methods This retrospective study analyzed 101 pathologically confirmed soft tissue masses (78 benign, 23 malignant) that ...
Lu Xie +12 more
wiley +1 more source
, 2018 Sporadic inclusion body myositis (IBM) is an acquired muscle disorder associated with ageing, for which there is no effective treatment. It is characterized by a typical early clinical phenotype with (often asymmetric) weakness of the knee extensors and ...
Pedro M. Machado
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In Vitro Fertilization is Essential Healthcare for Patients With Rheumatic Disease
ACR Open Rheumatology, Volume 8, Issue 7, July 2026.Infertility presents a profound physical, emotional, and financial burden, particularly for rheumatology patients who often face substantial barriers to family building. The 2024 Alabama Supreme Court ruling in LePage v. Center for Reproductive Medicine equating embryo destruction with wrongful death introduced new legal uncertainties, sparking ...
Amanda Moyer +4 more
wiley +1 more source
Primary Sjögren syndrome and inclusion body myositis
, 2009 The authors report the case of a 69-years-old woman with Sjögren's syndrome. After 8 years of disease she developed muscle weakness and the diagnosis of inclusion body myositis was established. This is a rare association.
Salvador, MJ +3 more
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Macroglossia in Inclusion Body Myositis
, 2017 OBJECTIVE: Discussion of a case of Inclusion body myositis (IBM) associated with macroglossia. INTRODUCTION: IBM is one of the idiopathic inflammatory myopathies.
Qin, Lan +2 more
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Az inclusiós testes myositis az idiopathiás inflammatorikus myopathiák vakuólaképződéssel járó formái közé tartozik, azok 15–28%-át képezi. Fontos a korai felismerés, mert alattomosan progrediáló betegségről van szó, és a már kialakult izomatrófia ...
Dankó, Katalin, Váncsa, Andrea
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JIMD Reports, Volume 67, Issue 4, July 2026.ABSTRACT Mitochondrial carbonic anhydrase VA (CA‐VA) deficiency is a rare inherited metabolic disorder caused by biallelic variants of the CA5A gene. It presents with hyperammonemia, lactic acidosis, and ketonuria, with or without hypoglycemia. We report the long‐term follow‐up of the first two reported cases of CA‐VA deficiency: a 16‐year‐old female ...
Shaymaa Shurrab +5 more
wiley +1 more source
Inclusion body myositis: New insights into pathogenesis
, 2008 Purpose of review: The pathogenesis of sporadic inclusion body myositis is complex and the disease has a relentless course. Recent observations regarding possible mechanisms of disease may provide targets for therapy.
Mastaglia, F.L. +3 more
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Ageing‐Associated Dysregulation of Myogenic Differentiation in Inclusion Body Myositis
Journal of Cachexia, Sarcopenia and MuscleSkeletal 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 +2 more
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