All Stories

  1. Disparities or Inequities in Newborn Screening (NBS) Programs
  2. Disparities or Inequities in Newborn Screening (NBS) Programs
  3. Disparities or Inequities in Newborn Screening (NBS) Programs
  4. Four Decades of Newborn Screening: A Historical Perspective of Laboratory Practices
  5. Dr. Louis Isaac Woolf: At the Forefront of Newborn Screening and the Diet to Treat Phenylketonuria-Biography to Mark His 100th Birthday
  6. Review and Proposal of Alternative Technologies for Comprehensive and Reliable Newborn Screening Using Paper Borne Urine Samples for Lysosomal Storage Disorders: Glycosphingolipid Disorders
  7. Dr. Louis Isaac Woolf: At the Forefront of Newborn Screening and the Diet to Treat Phenylketonuria—Biography to Mark His 100th Birthday †
  8. Pregnanetriolone in paper-borne urine for neonatal screening for 21-hydroxylase deficiency: The place of urine in neonatal screening
  9. Copper Nanowires Immobilized on the Boards of Microfluidic Chips for the Rapid and Simultaneous Diagnosis of Galactosemia Diseases in Newborn Urine Samples
  10. CHAPTER 12. Dietary Sugars: TLC Screening of Sugars in Urine and Blood Samples
  11. Congenital Hypothyroidism with Neurological and Respiratory Alterations: A Case Detected Using a Variable Diagnostic Threshold for Tsh
  12. Evaluation and long-term follow-up of infants with inborn errors of metabolism identified in an expanded screening programme
  13. Newborn screening in Spain, with particular reference to Galicia: Echoes of Louis I. Woolf
  14. Prevalence of maternal hepatitis C infection according to HIV serostatus in six Spanish regions (2003-2006)
  15. The TSH threshold in neonatal screening for congenital hypothyroidism: a variable solution
  16. Simple continuous TLC to separate sugars in urine and blood, Berry-Woolf and Guthrie specimens
  17. Procedure to determine GAG in urine eluate NBS in a very wide range of concentrations.
  18. Article Commentary: The contributions of Louis I Woolf to the treatment, early diagnosis and understanding of phenylketonuria
  19. Three novel mutations in the CFTR gene identified in Galician patients
  20. Tría neonatal de galactosemia: situación del ensayo en orina
  21. Selenium state of children. The selenium content of the serum of normal children and children with inborn errors of metabolism
  22. The determination of copper and zinc in microsamples of undeproteinized blood serum using atomic absorption spectrophotometry with direct flame injection
  23. The use of continuous thin layer chromatography in the study of mucopolysaccharidoses
  24. Application of Pelletized Sodium Borohydride in the Spectrophotometric Determination of Arsenic
  25. Continuos thin-layer chromatography of sugars of clinical interest in samples of urine impregnated on paper