Results 151 to 160 of about 4,757 (204)
Metabolic causes of myoglobinuria
Annals of Neurology, 1990 AbstractTo evaluate the proportion of cases of myoglobinuria that can be ascribed to specific metabolic defects, we have studied eight enzymes–phosphorylase, phosphorylase kinase, phosphofructokinase (PFK), phosphoglycerate kinase (PGK), phosphoglycerate mutase (PGAM), lactate dehydrogenase (LDH), carnitine palmitoyltransferase (CPT), and myoadenylate ...
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JAMA: The Journal of the American Medical Association, 1976 To the Editor.—I read the article titled "Recurrent Acute Renal Failure With Idiopathic Paroxysmal Myoglobinuria" (233:349-350, 1975) with considerable interest.
Kottil W. Rammohan, Rammohan, Kottil W
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Myoglobinuria in boys with Duchenne muscular dystrophy on corticosteroid therapy
Neuromuscular Disorders, 2008 Myoglobinuria is a recognised complication of Duchenne muscular dystrophy (DMD), but has only once been reported in ambulant boys on corticosteroid therapy [Dubowitz V, Kinali M, Main M, Mercuri E, Muntoni F. Remission of clinical signs in early Duchenne
M Eagle, Volker Straub
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Hypernatremia with myoglobinuria
The American Journal of the Medical Sciences, 1973Abstract:A patient with myoglobinuria and hypernatremia is presented. The effect of hypernatremia on muscle metabolism is discussed, and hypernatremia as a cause of myoglobinuria is suggested.
J M, Ulvila, V J, Nessan
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