Results 41 to 50 of about 4,758 (205)
Molecular Genetics and Metabolism Reports, 2021 A 29-year-old man developed, since the age of 18, exercise intolerance and exercise-induced rhabdomyolysis, with myoglobinuria. Muscle biopsy showed ragged-red fibers. Multiple mitochondrial DNA deletions were detected. The previously reported pathogenic
Carlos Pablo de Fuenmayor-Fernández de la Hoz +7 more
doaj +1 more source
Anaesthetic management of a horse with acute kidney injury
Equine Veterinary Education, EarlyView.Summary Anaesthetic management of animals with acute kidney injuries (AKI) is complex and poses considerable risk. There are no publications describing management of anaesthetised horses with AKI. Perioperative and anaesthetic care of a Thoroughbred filly presented with traumatic injuries and subsequent AKI is described.
C. T. Quinn, K. J. Hughes, A. N. Walton
wiley +1 more source
, 1968 Myoglobinuria is one of the important causes of acute renal failure, and its incidence may be increasing because of recent increase of motor vehicle accidents.
ハヂンス, ポールC. +1 more
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McArdle’s disease: A case of exercise intolerance and myopathy
Journal of Dr. NTR University of Health SciencesMcArdle disease is a hereditary glycogen storage disorder caused by a deficiency in the enzyme myophosphorylase, leading to impaired glycogen breakdown in skeletal muscles.
Prince Saha +2 more
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Veterinary Dermatology, EarlyView.Background: Oclacitinib is a Janus kinase inhibitor approved for the treatment of pruritus associated with allergic dermatitis in dogs and may be effective in horses. Objectives: To evaluate the efficacy of oclacitinib in reducing pruritus and skin lesions in horses with allergic dermatitis.
Maturawan Tunhikorn +6 more
wiley +1 more source
Increased creatinine kinase levels due to MDMA use without myoglobinuria and renal failure [MDMA kullanımı sonrası miyoglobinüri ve böbrek yetmezliǧi olmadan kreatin kinaz yüksekliǧi olan bir olgu sunumu] [PDF]
, 2012 We report a 15-year-old boy admitted to the pediatric emergency unit with acute encephalopathy associated with an elevated serum creatine kinase (CK) level without myoglobinuria and renal failure, which was due to 3,4- Methylenedioxymethamphetamine (MDMA)
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Clinical Genetics, Volume 110, Issue 1, Page 15-28, July 2026.Advances in genomic, proteomic, and transcriptomic technologies are transforming the diagnosis of genetic myopathies. When integrated with traditional muscle pathology, multi‐omics approaches improve diagnostic yield, clarify disease mechanisms, and support more precise, mechanism‐based therapeutic strategies for patients with neuromuscular disorders ...
Ludmila Alem +2 more
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Myoglobinuria and carnitine palmityltransferase (CPT) deficiency: Studies with malonyl-CoA suggest absence of only CPT-II [PDF]
, 1984 A 23-year-old man suffered since adolescence from recurrent myoglobinuria. His ketone body production during fasting was normal. Muscle, liver, and platelet carnitine palmityltransferase (CPT) ranged from 4 to 27% of control by isotope exchange and ...
Angelini C. +4 more
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Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT We present the case of a 78‐year‐old woman with metabolic syndrome and a history of multiple ischemic strokes who developed progressive symmetrical proximal muscle weakness, predominantly affecting the lower extremities, while on atorvastatin.
Nischal Shrestha +2 more
wiley +1 more source
Apollo Medicine, 2023 Background: Diabetic ketoacidosis (DKA) is an acute complication of diabetes mellitus, which is diagnosed by the triad of hyperglycemia, metabolic acidosis, and ketosis.
Rutvi Chahal +3 more
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