Recurrent myoglobinuria due to carnitine palmitoyltransferase II deficiency: expression of the molecular phenotype in cultured muscle cells
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference11 articles.
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3. Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death;Demaugre;J Clin Invest,1991
4. Lethal multiorgan deficiency of carnitine palmitoyltransferase II;Hug;N Eng J Med,1991
5. Malonyl-CoA binding site and the overt carnitine palmitoyltransferase reside on the opposite sides of the outer mitochondrial membrane;Murthy,1987
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2. Recurrent episodic myoglobinuric acute kidney injury as presenting manifestation of idiopathic polymyositis;Saudi Journal of Kidney Diseases and Transplantation;2018
3. Structure-Function Studies with the Mitochondrial Carnitine Palmitoyltransferases I and II;Monatshefte für Chemie - Chemical Monthly;2005-07-18
4. Recurrent rhabdomyolysis and myoglobinuric acute renal failure in a patient with polymyositis;Nephrology Dialysis Transplantation;2005-06-28
5. Carnitine Palmitoyltransferase II Deficiency: A Clinical, Biochemical, and Molecular Review;Laboratory Investigation;2003-11
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