000 01379 a2200409 4500
005 20250513025024.0
264 0 _c19810327
008 198103s 0 0 ger d
022 _a0036-7672
040 _aNLM
_beng
_cNLM
100 1 _aMarti, H R
245 0 0 _a[Clinical demonstrations of hereditary disorders of metabolism].
_h[electronic resource]
260 _bSchweizerische medizinische Wochenschrift
_cDec 1980
300 _a1857-63 p.
_bdigital
500 _aPublication Type: Case Reports; English Abstract; Journal Article
650 0 4 _aAdenosine Triphosphate
_xmetabolism
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAnemia, Hemolytic
_xetiology
650 0 4 _aAnesthesia, General
_xadverse effects
650 0 4 _aErythrocytes
_xmetabolism
650 0 4 _aFemale
650 0 4 _aHemoglobinuria, Paroxysmal
_xgenetics
650 0 4 _aHeterozygote
650 0 4 _aHumans
650 0 4 _aLipid Metabolism
650 0 4 _aMale
650 0 4 _aMalignant Hyperthermia
_xetiology
650 0 4 _aMetabolic Diseases
_xgenetics
650 0 4 _aMiddle Aged
650 0 4 _aMyoglobinuria
_xgenetics
650 0 4 _aPhysical Exertion
650 0 4 _aPyruvate Kinase
_xdeficiency
650 0 4 _aSickle Cell Trait
_xcomplications
650 0 4 _aThalassemia
_xcomplications
773 0 _tSchweizerische medizinische Wochenschrift
_gvol. 110
_gno. 49
_gp. 1857-63
999 _c7455133
_d7455133