Results 21 to 30 of about 988,052 (165)
Basic requirements to establish a neuromuscular laboratory
Indian Journal of Pathology and Microbiology, 2022 Histopathological analysis of muscle biopsy is a prerequisite in the evaluation of neuromuscular disorders, particularly inflammatory myopathies, metabolic myopathies, congenital myopathies, muscular dystrophies and differentiating myopathies and ...
Bevinahalli N Nandeesh +2 more
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Electron microscopy in the diagnosis of skeletal muscle disorders: Its utility and limitations
Indian Journal of Pathology and Microbiology, 2022 Electron microscopy (EM) has a substantial role in the diagnosis of skeletal muscle disorders. The ultrastructural changes can be observed in muscle fibers and other components of the muscle tissue. EM serves as a confirmatory tool where the diagnosis is
Rashmi Santhoshkumar +1 more
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The Role of Incubation Conditions in the Onset of Avian Myopathies
Frontiers in Physiology, 2020 White striping, wooden breast, and spaghetti muscle have become common myopathies in broilers worldwide. Several research reports have indicated that the origin of these lesions is metabolic disorders.
Edgar Orlando Oviedo-Rondón +2 more
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A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy
EMBO Molecular Medicine, 2023 Mitochondrial diseases are a heterogeneous group of monogenic disorders that result from impaired oxidative phosphorylation (OXPHOS). As neuromuscular tissues are highly energy‐dependent, mitochondrial diseases often affect skeletal muscle.
Nneka Southwell +15 more
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Prospect of early vascular tone and satellite cell modulations on white striping muscle myopathy
Poultry Science, 2021 Polyphasic myodegeneration potentially causes severe physiological and metabolic disorders in the breast muscle of fast-growing broiler chickens. To date, the etiology of recent muscle myopathies, such as the white striping (WS) phenotype, is still ...
Hammed Ayansola +5 more
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Stepwise Approach to Myopathy in Systemic Disease
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
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Frontiers in Physiology, 2021 Carnitine palmitoyltransferase II (CPTII) deficiency is the most frequent inherited disorder regarding muscle fatty acid metabolism, resulting in a reduced mitochondrial long-chain fatty acid oxidation during endurance exercise. This condition leads to a
Massimo Negro +9 more
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Electromyography and Metabolic Myopathies
Pediatric Neurology Briefs, 2014 Investigators at the Mayo Clinic, Rochester, MN, report the sensitivity and specificity of the pediatric EMG in the diagnosis of myopathic disorders in patients
J Gordon Millichap, John J Millichap
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History of international connections of myology in Europe
European Journal of Translational Myology, 2023 Over the past centuries, myology as a basic and clinical science has passed through three major stages of development: the classical period, the modern nosographic stage, and the molecular era.
Corrado Angelini
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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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