000 01626 a2200481 4500
005 20250517025852.0
264 0 _c20160121
008 201601s 0 0 eng d
022 _a1750-1172
024 7 _a10.1186/s13023-015-0259-0
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGuffon, Nathalie
245 0 0 _aDiagnosis, quality of life, and treatment of patients with Hunter syndrome in the French healthcare system: a retrospective observational study.
_h[electronic resource]
260 _bOrphanet journal of rare diseases
_cApr 2015
300 _a43 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aData Collection
650 0 4 _aDelivery of Health Care
650 0 4 _aEnzyme Replacement Therapy
650 0 4 _aFemale
650 0 4 _aFrance
_xepidemiology
650 0 4 _aHumans
650 0 4 _aIduronate Sulfatase
_xtherapeutic use
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMucopolysaccharidosis II
_xdrug therapy
650 0 4 _aQuality of Life
650 0 4 _aRetrospective Studies
650 0 4 _aSurveys and Questionnaires
650 0 4 _aYoung Adult
700 1 _aHeron, Bénédicte
700 1 _aChabrol, Brigitte
700 1 _aFeillet, François
700 1 _aMontauban, Vincent
700 1 _aValayannopoulos, Vassili
773 0 _tOrphanet journal of rare diseases
_gvol. 10
_gp. 43
856 4 0 _uhttps://doi.org/10.1186/s13023-015-0259-0
_zAvailable from publisher's website
999 _c24818043
_d24818043