000 01414 a2200421 4500
005 20250512222119.0
264 0 _c19830415
008 198304s 0 0 eng d
022 _a0031-3998
024 7 _a10.1203/00006450-198302000-00015
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBrivet, M
245 0 0 _aDefective galactose oxidation in a patient with glycogen storage disease and Fanconi syndrome.
_h[electronic resource]
260 _bPediatric research
_cFeb 1983
300 _a157-61 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aChild, Preschool
650 0 4 _aErythrocytes
_xmetabolism
650 0 4 _aFanconi Syndrome
_xcomplications
650 0 4 _aFemale
650 0 4 _aGalactose
_xmetabolism
650 0 4 _aGlucagon
650 0 4 _aGlucose
_xmetabolism
650 0 4 _aGlycogen Storage Disease
_xcomplications
650 0 4 _aGlycolysis
650 0 4 _aHumans
650 0 4 _aIn Vitro Techniques
650 0 4 _aKidney
_xmetabolism
650 0 4 _aLiver
_xmetabolism
650 0 4 _aLiver Function Tests
650 0 4 _aOxidation-Reduction
700 1 _aMoatti, N
700 1 _aCorriat, A
700 1 _aLemonnier, A
700 1 _aOdievre, M
773 0 _tPediatric research
_gvol. 17
_gno. 2
_gp. 157-61
856 4 0 _uhttps://doi.org/10.1203/00006450-198302000-00015
_zAvailable from publisher's website
999 _c6572186
_d6572186