Results 101 to 110 of about 46,680 (279)

Pathogenic and rare deleterious variants in multiple genes suggest oligogenic inheritance in recurrent exertional rhabdomyolysis

open access: yesMolecular Genetics and Metabolism Reports, 2018
Exertional rhabdomyolysis is a metabolic event characterized by the release of muscle content into the circulation due to exercise-driven breakdown of skeletal muscle.
Nyamkhishig Sambuughin   +9 more
doaj  

Status epilepticus in older adults: A critical review

open access: yesEpilepsia, EarlyView.
Abstract Older adults (≥60 years of age) have the highest incidence of status epilepticus (SE) among adults and experience the highest morbidity and mortality. SE incidence increases with age in adulthood. A recent study from Austria estimated an incidence of 89.6/100 000 and 67.6/100 000 person‐years adjusted for age and sex in women and men aged >60 ...
Matthew R. Woodward   +5 more
wiley   +1 more source

Rhabdomyolysis

open access: yesBMJ, 2003
The dramatic title–Rhabdomyolysis: the hidden killer–given to a recent review of this condition emphasised that dissolution of striated muscle fibres, with leakage of muscle enzymes, myoglobin, potassium, calcium, and other intracellular constituents, can occur in anyone under particular circumstances and that the consequences can be severe and ...
Malcolm J. Phillips, Russell Lane
openaire   +3 more sources

Assessment of tree‐associated atypical myopathy risk factors in Acer pseudoplatanus (sycamore) seeds and leaves

open access: yesEquine Veterinary Journal, EarlyView.
Abstract Background Sycamore tree‐derived hypoglycin A (HGA) toxin causes atypical myopathy (AM), an acute, equine pasture‐associated rhabdomyolysis but incidence fluctuates. Objectives Investigate whether tree or environmental factors influence HGA concentration in sycamore material and are associated with AM relative risk.
Sonia González‐Medina   +3 more
wiley   +1 more source

Rhabdomyolysis in 114 patients with acute poisonings

open access: yesJournal of Research in Medical Sciences, 2015
Background: Rhabdomyolysis is a clinical and biochemical syndrome, which is observed in some patients with acute chemical and/or pharmaceutical poisonings.
Seyed Reza Mousavi   +6 more
doaj  

Acute rhabdomyolysis in a young woman with moderate COVID-19

open access: yesIDCases, 2021
The coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is having serious medical, social, and economic impacts worldwide.
Kohei Fujita   +6 more
doaj  

Chronic idiopathic myopathy in Icelandic horses: A case series

open access: yesEquine Veterinary Journal, EarlyView.
Abstract Background Exertional myopathies are recognised as a cause of poor performance in equines. In Icelandic horses presenting reduced performance and/or multi‐limb lameness, no specific myopathy has been identified. Objectives To characterise the clinical presentation and histopathological findings in muscle biopsy samples from Icelandic horses ...
Sanni Hansen   +6 more
wiley   +1 more source

Rhabdomyolysis-Induced Acute Kidney Injury in Diabetic Emergency: Underdiagnosed and an Important Association to Be Aware of

open access: yesCase Reports in Medicine, 2018
Rhabdomyolysis is a potentially life-threatening clinical syndrome associated with muscle injury which can cause a leakage of intracellular contents, manifested from the range of being asymptomatic to a life-threatening condition causing acute kidney ...
Ami Amin   +6 more
doaj   +1 more source

Delayed presentation of severe rhabdomyolysis leading to acute kidney injury following atorvastatin-gemfibrozil combination therapy: a case report

open access: yesJournal of Medical Case Reports, 2018
Background Rhabdomyolysis is a rare but serious complication of lipid-lowering therapy. Statin and fibrate combination increases the risk of rhabdomyolysis possibly by pharmacodynamic interactions.
Chamara Dalugama   +2 more
doaj   +1 more source

Effects of HMG CoA reductase (HMGCR) deficiency on skeletal muscle development

open access: yesThe FEBS Journal, EarlyView.
Three skeletal muscle diseases are linked to HMGCR, a key enzyme in cholesterol synthesis. These diseases include a muscular dystrophy associated with pathogenic variants in the HMGCR gene, statin‐associated myopathy, and autoimmune anti‐HMGCR myopathy.
Mekala Gunasekaran   +20 more
wiley   +1 more source

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