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Analytical Methods : Advancing Methods and Applications|August 4, 2023
Development of a kit for urine collection on filter paper as an alternative for Pompe disease screening and monitoring by LC-HRMSHygor M R de Souza, Fernanda B Scalco, Rafael Garrett, et al.
Bioanalysis|January 22, 2011
Plasma volume expanders: use in medicine and detecting misuse in sportsRuth E Simoni, Fernanda B Scalco, Maria Lucia C de Oliveira, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 10, 2023
Untargeted LC-HRMS metabolomics reveals candidate biomarkers for mucopolysaccharidosesClarisse L Torres, Fernanda B Scalco, Maria Lúcia C de Oliveira, et al.
Journal of Science and Medicine in Sport|September 5, 2008
Screening for hydroxyethyl starch (HES) doping in sportFernanda B Scalco, Ruth E Simoni, Maria Lucia C de Oliveira, et al.
Journal of Inherited Metabolic Disease|June 16, 2010
Fumaric aciduria: an overview and the first Brazilian case reportGabriella Allegri, Marcia J Fernandes, Fernanda B Scalco, et al.
Metabolomics : Official Journal of the Metabolomic Society|March 29, 2023
Combined targeted and untargeted high-resolution mass spectrometry analyses to investigate metabolic alterations in pompe diseaseMariana B M de Moraes, Hygor M R de Souza, Maria L C de Oliveira, et al.
Drug Testing and Analysis|June 27, 2015
Systematic analysis of glycerol: colourimetric screening and gas chromatography-mass spectrometric confirmationVinícius F Sardela, Fernanda B Scalco, Karina M Cavalcante, et al.
Anais Da Academia Brasileira De Ciencias|October 11, 2018
L-carnitine supplementation in the recovery of plasma L-carnitine in patients with heart failure submitted to coronary artery bypass graftingWanise M Souza Cruz, Sheila M S Guimarães, Gabrielle C Maciel, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Early hematopoietic stem cell transplantation in a patient with severe mucopolysaccharidosis II: A 7 years follow-upAnneliese L Barth, Tatiana S P C de Magalhães, Ana Beatriz R Reis, et al.
Journal of Medical Genetics|July 5, 2022
Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylationShino Shimada, Bobby G Ng, Amy L White, et al.
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