Results 11 to 20 of about 1,023,457 (221)
Metabolic myopathy presenting with polyarteritis nodosa: a case report [PDF]
Journal of Medical Case Reports, 2011 Introduction To the best of our knowledge, we describe for the first time a patient in whom an unusual metabolic myopathy was identified after failure to respond to curative therapy for a systemic vasculitis, polyarteritis nodosa.
Elbalkhi Amro +3 more
doaj +2 more sources
Lipid Storage Myopathy in Behçet's Disease: A Rare Cause of Elevated Serum Creatine Kinases Levels [PDF]
Case Reports in Rheumatology, 2012 Muscular involvement in Behçet’s disease is rare and there are only a few case reports in the literature. The causes of elevated muscle enzymes in a patient with Behcet’s disease are many, including myositis, drug-induced myopathy, metabolic myopathy ...
Sedat Yilmaz +6 more
doaj +2 more sources
Evidence-based treatment of metabolic myopathy
Chinese Journal of Contemporary Neurology and Neurosurgery, 2014 Objective To evaluate the current treatments and possible adverse reactions of metabolic myopathy, and to develop the best solution for evidence-based treatment.
Yan LIN, Wen-wu ZHANG, Ling LIU
doaj +1 more source
Research progress of electrophysiology for the diagnosis of metabolic myopathy
Chinese Journal of Contemporary Neurology and Neurosurgery, 2014 Metabolic myopathies comprise a group of diverse disorders characterized by defects ofn energy metabolism in skeletal muscle cells, including glycogen storage disease (GSD), lipid storage myopathy (LSM) and mitochondrial myopathy.
Lei ZHAO, Li⁃ying CUI
doaj +1 more source
Clinical Approach to Metabolic Myopathies
Pediatric Neurology Briefs, 2000 The clinical and laboratory evaluation of the patient with suspected metabolic myopathy is reviewed from the Department of Neurology, Children’s Hospital, Boston, MA.
J Gordon Millichap
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Stepwise Approach to Myopathy in Systemic Disease [PDF]
Frontiers in Neurology, 2011 Muscle diseases can constitute a large variety of both acquired and hereditary disorders. Myopathies in systemic disease results from several different disease processes including endocrine, inflammatory, paraneoplastic, infectious, drug and toxin ...
Jasvinder eChawla
doaj +2 more sources
Hypocalcemic myopathy without tetany due to idiopathic hypoparathyroidism: case report [PDF]
Arquivos de Neuro-Psiquiatria, 2004 Myopathy due to idiopathic hypoparathyroidism is very unusual. We report on a 30 years-old man referred with complaints of sporadic muscle pain and mild global weakness for 10 years.
Daniel Bocchese Nora +3 more
doaj +2 more sources
A Nonsense Variant in the ACADVL Gene in German Hunting Terriers with Exercise Induced Metabolic Myopathy. [PDF]
G3 (Bethesda), 2018 Several enzymes are involved in fatty acid oxidation, which is a key process in mitochondrial energy production. Inherited defects affecting any step of fatty acid oxidation can result in clinical disease.
Lepori V +12 more
europepmc +3 more sources
RUNX1-Mediated Hypoxic Signaling Impairs Myogenesis and Promotes Fibrosis in Myopathies. [PDF]
Adv Sci (Weinh)Myofiber overgrowth was associated with reduced blood flow and a potential hypoxic state in broiler breast muscle, accompanied by increased RUNX1 expression. Elevated RUNX1 impaired myogenic regeneration, promoted fibrosis, and disrupted the signaling niche required for efficient muscle repair, contributing to pathological degeneration in Wooden Breast
Zhao L, Hou T, Zhang L, Gao F, Xing T.
europepmc +2 more sources
Thyrotoxic myopathy: research status, diagnosis, and treatment [PDF]
, 2022 Thyrotoxic myopathy is hyperthyroidism accompanied by muscle lesions. It is recognized as the general term for a group of symptoms with several main manifestations of several hyperthyroidism patients in the course (e.g. muscle weakness, muscle paralysis,
Cui, Han; Department of Endocrinology, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People’s Hospital), Dongguan, China +3 more
core +1 more source