000			01469 a2200421 4500
005			20250514224719.0
264		0	_c20050607
008			200506s 0 0 eng d
022			_a0803-5253
024	7		_a10.1111/j.1651-2227.2005.tb01787.x _2doi
040			_aNLM _beng _cNLM
100	1		_aHolub, M
245	0	0	_aLack of correlation between fatty acid oxidation disorders and haemolysis, elevated liver enzymes, low platelets (HELLP) syndrome? _h[electronic resource]
260			_bActa paediatrica (Oslo, Norway : 1992) _cJan 2005
300			_a48-52 p. _bdigital
500			_aPublication Type: Journal Article; Multicenter Study
650	0	4	_a3-Hydroxyacyl CoA Dehydrogenases _xdeficiency
650	0	4	_aAdult
650	0	4	_aCarnitine _xanalogs & derivatives
650	0	4	_aCase-Control Studies
650	0	4	_aDNA Mutational Analysis
650	0	4	_aFemale
650	0	4	_aHELLP Syndrome _xetiology
650	0	4	_aHumans
650	0	4	_aInfant, Newborn
650	0	4	_aMale
650	0	4	_aMetabolism, Inborn Errors _xcomplications
650	0	4	_aPregnancy
650	0	4	_aRetrospective Studies
650	0	4	_aRisk Factors
700	1		_aBodamer, O A
700	1		_aItem, C
700	1		_aMühl, A
700	1		_aPollak, A
700	1		_aStöckler-Ipsiroglu, S
773	0		_tActa paediatrica (Oslo, Norway : 1992) _gvol. 94 _gno. 1 _gp. 48-52
856	4	0	_uhttps://doi.org/10.1111/j.1651-2227.2005.tb01787.x _zAvailable from publisher's website
999			_c15525759 _d15525759