Muscle MRI in patients with long-chain fatty acid oxidation disorders

Journal of Inherited Metabolic Disease

Volumn 37, Issue 3, 2014, Pages 405-413

  Diekman, Eugene F ^a,b   Van Der Pol, W Ludo ^c   Nievelstein, Rutger A J ^c   Houten, Sander M ^b   Wijburg, Frits A ^b   Visser, Gepke ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^b UNIVERSITY OF AMSTERDAM   (Netherlands)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

CREATINE KINASE; 3 HYDROXYACYL COENZYME A DEHYDROGENASE; CARNITINE PALMITOYLTRANSFERASE; FATTY ACID; LONG CHAIN ACYL COENZYME A DEHYDROGENASE;

ADOLESCENT; ADULT; ARTICLE; CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; CREATINE KINASE BLOOD LEVEL; DISEASE ASSOCIATION; DISEASE COURSE; EXERCISE; FEMALE; GASTROCNEMIUS MUSCLE; GLUTEUS MAXIMUS MUSCLE; HUMAN; INBORN ERROR OF METABOLISM; LIPID STORAGE; LONG CHAIN FATTY ACID OXIDATION DISORDER; LONG CHAIN HYDROXYACYL COA DEHYDROGENASE DEFICIENCY; MALE; MITOCHONDRIAL TRIFUNCTIONAL PROTEIN DEFICIENCY; MUSCLE; MUSCLE FUNCTION; MUSCLE STRENGTH; MUSCLE WEAKNESS; MYALGIA; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEAR MAGNETIC RESONANCE SCANNER; PERONEUS MUSCLE; RADIOLOGICAL PARAMETERS; RHABDOMYOLYSIS; SEMITENDINOUS MUSCLE; SOLEUS MUSCLE; STIR SIGNAL INTENSITY; T1W SIGNAL INTENSITY; TENSOR FASCIA LATA MUSCLE; TIBIALIS ANTERIOR MUSCLE; VASTUS LATERALIS MUSCLE; VERY LONG CHAIN ACYL COA DEHYDROGENASE DEFICIENCY; BLOOD; CARDIOMYOPATHY; DEFICIENCY; DISORDERS OF LIPID AND LIPOPROTEIN METABOLISM; DISORDERS OF MITOCHONDRIAL FUNCTIONS; METABOLISM; MIDDLE AGED; MITOCHONDRIAL MYOPATHY; MUSCLE DISEASE; NEUROLOGIC DISEASE; OXIDATION REDUCTION REACTION; PATHOLOGY; PRESCHOOL CHILD; PROCEDURES; SKELETAL MUSCLE;

3-HYDROXYACYL COA DEHYDROGENASES; ACYL-COA DEHYDROGENASE, LONG-CHAIN; ADOLESCENT; ADULT; CARDIOMYOPATHIES; CARNITINE O-PALMITOYLTRANSFERASE; CHILD; CHILD, PRESCHOOL; CREATINE KINASE; FATTY ACIDS; FEMALE; HUMANS; LIPID METABOLISM, INBORN ERRORS; MAGNETIC RESONANCE IMAGING; MALE; METABOLISM, INBORN ERRORS; MIDDLE AGED; MITOCHONDRIAL DISEASES; MITOCHONDRIAL MYOPATHIES; MUSCLE, SKELETAL; MUSCULAR DISEASES; NERVOUS SYSTEM DISEASES; OXIDATION-REDUCTION; RHABDOMYOLYSIS;

EID: 84904190926     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-013-9666-3     Document Type: Article

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