000 01487 a2200433 4500
005 20250510195727.0
264 0 _c19761223
008 197612s 0 0 eng d
022 _a0547-6844
040 _aNLM
_beng
_cNLM
100 1 _aNadler, H L
245 0 0 _aCurrent status of treatment in storage disorders.
_h[electronic resource]
260 _bBirth defects original article series
_c1976
300 _a177-88 p.
_bdigital
500 _aPublication Type: Journal Article; Review
650 0 4 _aAnimals
650 0 4 _aAspergillus niger
650 0 4 _aCerebroside-Sulfatase
_xtherapeutic use
650 0 4 _aChild, Preschool
650 0 4 _aCystinosis
_xsurgery
650 0 4 _aEnzyme Induction
650 0 4 _aFabry Disease
_xtherapy
650 0 4 _aGangliosidoses
_xtherapy
650 0 4 _aGaucher Disease
_xtherapy
650 0 4 _aGlucosidases
_xtherapeutic use
650 0 4 _aGlucuronidase
_xtherapeutic use
650 0 4 _aGlycogen Storage Disease
_xsurgery
650 0 4 _aHepatolenticular Degeneration
_xsurgery
650 0 4 _aHumans
650 0 4 _aKidney Transplantation
650 0 4 _aLeukodystrophy, Metachromatic
_xtherapy
650 0 4 _aLiver Transplantation
650 0 4 _aMetabolism, Inborn Errors
_xtherapy
650 0 4 _aMucopolysaccharidoses
_xtherapy
650 0 4 _aNiemann-Pick Diseases
_xsurgery
650 0 4 _aPortacaval Shunt, Surgical
650 0 4 _aTransplantation, Homologous
773 0 _tBirth defects original article series
_gvol. 12
_gno. 6
_gp. 177-88
999 _c9458
_d9458