Claudio Sampaio Filho

Investigation of newborns with abnormal results in a newborn screening program for four lysosomal storage diseases in Brazil

E. C. Neto, R. Giugliani, A. Brusius-Facchin, 2017, Molecular genetics and metabolism reports.

Pseudo deficiency of acid α-glucosidase: a challenge in the newborn screening for Pompe diseases

E. C. Neto, R. Giugliani, A. Brusius-Facchin, 2017 .