Daisy E. Castineiras
A Coruna, GA, Spain
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 12 publications
A newborn Screening Programme for Inborn errors of metabolism in Galicia: 22 years of evaluation and follow-up.
Journal: Orphanet journal of rare diseases
Published: September 20, 2023
Reference values of amino acids, acylcarnitines and succinylacetone by tandem mass spectrometry for use in newborn screening in southwest Colombia.
Journal: Colombia medica (Cali, Colombia)
Published: December 08, 2017
Corrigendum to "Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening" [Mol. Genet. Metab. 110 (2013) 218-221].
Journal: Molecular genetics and metabolism
Published: April 17, 2015
Corrigendum to "A glimpse into past, present, and future DNA sequencing" [Mol. Genet. Metab. 110 (2013) 3-24].
Journal: Molecular genetics and metabolism
Published: April 17, 2015
The early detection of Salla disease through second-tier tests in newborn screening: how to face incidental findings.
Journal: European journal of medical genetics
Published: April 26, 2014
Birth Prevalence of Fatty Acid β-Oxidation Disorders in Iberia.
Journal: JIMD reports
Published: April 16, 2014
Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders.
Journal: Orphanet journal of rare diseases
Published: October 16, 2013
Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening.
Journal: Molecular genetics and metabolism
Published: July 11, 2013
Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: regional experience and high incidence of carnitine deficiency.
Journal: Orphanet journal of rare diseases
Published: March 07, 2013
A glimpse into past, present, and future DNA sequencing.
Journal: Molecular genetics and metabolism
Published: February 27, 2013
Development of electrospray ionization tandem mass spectrometry methods for the study of a high number of urine markers of inborn errors of metabolism.
Journal: Rapid communications in mass spectrometry : RCM
Published: August 14, 2012
Glutaric aciduria type I: outcome of patients with early- versus late-diagnosis.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: June 07, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026