Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges.
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NF1 is a critical regulator of muscle development and metabolismA thermolabile aldolase A mutant causes fever-induced recurrent rhabdomyolysis without hemolytic anemia.Ablation of steroid receptor coactivator-3 resembles the human CACT metabolic myopathyAcquired multiple acyl-CoA dehydrogenase deficiency and marked selenium deficiency causing severe rhabdomyolysis in a horse.Metabolic Encephalopathy and Lipid Storage Myopathy Associated with a Presumptive Mitochondrial Fatty Acid Oxidation Defect in a Dog.Lipid storage myopathy with clinical markers of Marfan syndrome: A rare associationSites of superoxide and hydrogen peroxide production during fatty acid oxidation in rat skeletal muscle mitochondria.Peripheral leukocyte anomaly detected with routine automated hematology analyzer sensitive to adipose triglyceride lipase deficiency manifesting neutral lipid storage disease with myopathy/triglyceride deposit cardiomyovasculopathyRecent advances in clinical neurogenetics.Inborn errors of cytoplasmic triglyceride metabolism.A diagnostic approach to recurrent myalgia and rhabdomyolysis in children.Acute rhabdomyolysis and inflammation.Metabolic Myoglobinuria.McArdle disease: a "pediatric" disorder presenting in an adult with acute kidney injury.Muscle MRI in patients with long-chain fatty acid oxidation disorders.Myopathology of Adult and Paediatric Mitochondrial Diseases.Variability in the clinical management of fatty acid oxidation disorders: results of a survey of Canadian metabolic physicians.Successful weight loss in two adult patients diagnosed with late-onset long-chain Fatty Acid oxidation defectTreatment Opportunities in Patients With Metabolic Myopathies.Mitochondrial trifunctional protein deficiency: a rare cause of adult-onset rhabdomyolysis.Fulminant lipid storage myopathy due to multiple acyl-coenzyme a dehydrogenase deficiency.The phenotypic spectrum of neutral lipid storage myopathy due to mutations in the PNPLA2 gene.CSI position statement on management of heart failure in IndiaStudy of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia
P2860
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P2860
Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges.
description
article científic
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article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 05 August 2010
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vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges.
@en
Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges.
@nl
type
label
Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges.
@en
Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges.
@nl
prefLabel
Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges.
@en
Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges.
@nl
P1476
Disorders of muscle lipid metabolism: diagnostic and therapeutic challenges.
@en
P2093
Christine Vianey-Saban
Pascal Laforêt
P304
P356
10.1016/J.NMD.2010.06.018
P577
2010-08-05T00:00:00Z