Introduction to the newborn screening, diagnosis, and treatment for pompe disease guidance supplement

Kishnani P.S.WUH-LIANG HWU2020-12-162020-12-1620170031-4005https://www.scopus.com/inward/record.uri?eid=2-s2.0-85021809281&doi=10.1542%2fpeds.2016-0280B&partnerID=40&md5=ae03f89d91842117fb033577fb8e1607https://scholars.lib.ntu.edu.tw/handle/123456789/525829[SDGs]SDG3diagnostic accuracy; diagnostic test; follow up; genetic counseling; glycogen storage disease type 2; health care policy; human; medical care; newborn; newborn screening; patient monitoring; practice guideline; priority journal; Review; screening; diagnostic imaging; dietary supplement; glycogen storage disease type 2; newborn screening; procedures; Diagnostic Imaging; Dietary Supplements; Glycogen Storage Disease Type II; Humans; Infant, Newborn; Neonatal ScreeningIntroduction to the newborn screening, diagnosis, and treatment for pompe disease guidance supplementreview10.1542/peds.2016-0280B291626722-s2.0-85021809281