000 01523 a2200469 4500
005 20250518032443.0
264 0 _c20200812
008 202008s 0 0 eng d
022 _a1399-0004
024 7 _a10.1111/cge.13546
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGermain, Dominique P
245 0 0 _aConsensus recommendations for diagnosis, management and treatment of Fabry disease in paediatric patients.
_h[electronic resource]
260 _bClinical genetics
_c08 2019
300 _a107-117 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650 0 4 _aAge Factors
650 0 4 _aAge of Onset
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aClinical Decision-Making
650 0 4 _aCombined Modality Therapy
650 0 4 _aConsensus
650 0 4 _aDisease Management
650 0 4 _aEnzyme Replacement Therapy
650 0 4 _aFabry Disease
_xdiagnosis
650 0 4 _aHumans
650 0 4 _aMonitoring, Physiologic
650 0 4 _aPhenotype
650 0 4 _aPractice Guidelines as Topic
650 0 4 _aSymptom Assessment
700 1 _aFouilhoux, Alain
700 1 _aDecramer, Stéphane
700 1 _aTardieu, Marine
700 1 _aPillet, Pascal
700 1 _aFila, Marc
700 1 _aRivera, Serge
700 1 _aDeschĂȘnes, Georges
700 1 _aLacombe, Didier
773 0 _tClinical genetics
_gvol. 96
_gno. 2
_gp. 107-117
856 4 0 _uhttps://doi.org/10.1111/cge.13546
_zAvailable from publisher's website
999 _c29546372
_d29546372