000			02059 a2200565 4500
005			20250516183924.0
264		0	_c20150220
008			201502s 0 0 eng d
022			_a1573-2665
024	7		_a10.1007/s10545-013-9666-3 _2doi
040			_aNLM _beng _cNLM
100	1		_aDiekman, Eugene F
245	0	0	_aMuscle MRI in patients with long-chain fatty acid oxidation disorders. _h[electronic resource]
260			_bJournal of inherited metabolic disease _cMay 2014
300			_a405-13 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_a3-Hydroxyacyl CoA Dehydrogenases _xdeficiency
650	0	4	_aAcyl-CoA Dehydrogenase, Long-Chain _xdeficiency
650	0	4	_aAdolescent
650	0	4	_aAdult
650	0	4	_aCardiomyopathies _xpathology
650	0	4	_aCarnitine O-Palmitoyltransferase _xdeficiency
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aCongenital Bone Marrow Failure Syndromes
650	0	4	_aCreatine Kinase _xblood
650	0	4	_aFatty Acids _xmetabolism
650	0	4	_aFemale
650	0	4	_aHumans
650	0	4	_aLipid Metabolism, Inborn Errors _xpathology
650	0	4	_aMagnetic Resonance Imaging _xmethods
650	0	4	_aMale
650	0	4	_aMetabolism, Inborn Errors _xpathology
650	0	4	_aMiddle Aged
650	0	4	_aMitochondrial Diseases _xpathology
650	0	4	_aMitochondrial Myopathies _xpathology
650	0	4	_aMitochondrial Trifunctional Protein _xdeficiency
650	0	4	_aMuscle, Skeletal _xpathology
650	0	4	_aMuscular Diseases _xpathology
650	0	4	_aNervous System Diseases _xpathology
650	0	4	_aOxidation-Reduction
650	0	4	_aRhabdomyolysis _xpathology
700	1		_avan der Pol, W Ludo
700	1		_aNievelstein, Rutger A J
700	1		_aHouten, Sander M
700	1		_aWijburg, Frits A
700	1		_aVisser, Gepke
773	0		_tJournal of inherited metabolic disease _gvol. 37 _gno. 3 _gp. 405-13
856	4	0	_uhttps://doi.org/10.1007/s10545-013-9666-3 _zAvailable from publisher's website
999			_c23336490 _d23336490