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Metabolic causes of myoglobinuria [PDF]
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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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
openaire +2 more sources
Myoglobinuria in boys with Duchenne muscular dystrophy on corticosteroid therapy [PDF]
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
Volker Straub, M Eagle
exaly +1 more source

