Cargando…
Neonatal screening for four lysosomal storage diseases with a digital microfluidics platform: Initial results in Brazil
We describe the initial results of a neonatal screening program for four lysosomal storage diseases (MPS I, Pompe, Gaucher and Fabry) using the digital microfluidics methodology. The method successfully identified patients previously diagnosed with these diseases and was used to test dried blood spo...
Autores principales: | Camargo, Eurico, Schulte, Jaqueline, Pereira, Jamile, Bravo, Heydy, Sampaio-Filho, Claudio, Giugliani, Roberto |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Genética
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6082237/ https://www.ncbi.nlm.nih.gov/pubmed/29870571 http://dx.doi.org/10.1590/1678-4685-GMB-2017-0227 |
Ejemplares similares
-
Investigation of newborns with abnormal results in a newborn screening program for four lysosomal storage diseases in Brazil
por: Bravo, Heydy, et al.
Publicado: (2017) -
Newborn screening for lysosomal disorders in Brazil: A pilot study using customized fluorimetric assays
por: Bender, Fernanda, et al.
Publicado: (2020) -
Newborn Screening for Congenital Infectious Diseases
por: Neto, Eurico Camargo, et al.
Publicado: (2004) -
Relative frequency and estimated minimal frequency of Lysosomal Storage
Diseases in Brazil: Report from a Reference Laboratory
por: Giugliani, Roberto, et al.
Publicado: (2017) -
Population analysis of the GLB1 gene in South Brazil
por: Baiotto, Cléia, et al.
Publicado: (2011)