249 results on '"Wiley, Veronica"'
Search Results
2. Association of elevated neonatal thyroid-stimulating hormone levels with school performance and stimulant prescription for attention deficit hyperactivity disorder in childhood
3. The implementation of newborn screening for spinal muscular atrophy: the Australian experience
4. Genotyping in patients with congenital adrenal hyperplasia by sequencing of newborn bloodspot samples
5. Progress in treatment and newborn screening for Duchenne muscular dystrophy and spinal muscular atrophy
6. Outcomes of lowered newborn screening thresholds for congenital hypothyroidism
7. Differences in Outcomes between Early and Late Diagnosis of Cystic Fibrosis in the Newborn Screening Era
8. Expanding the Australian Newborn Blood Spot Screening Program using genomic sequencing: do we want it and are we ready?
9. Newborn screening for spinal muscular atrophy in Australia: a non-randomised cohort study
10. Association between borderline neonatal thyroid-stimulating hormone concentrations and educational and developmental outcomes: a population-based record-linkage study
11. Long-Term Outcomes of Children with Intermediate Sweat Chloride Values in Infancy
12. Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment
13. Homocysteine Measurement in Dried Blood Spot for Neonatal Detection of Homocystinurias
14. Fifty years of newborn screening for congenital hypothyroidism: current status in Australasia and the case for harmonisation
15. Economic Evaluation of Newborn Screening for Severe Combined Immunodeficiency
16. Modelling the Cost-Effectiveness and Budget Impact of a Newborn Screening Program for Spinal Muscular Atrophy and Severe Combined Immunodeficiency
17. Neonatal vitamin D status and childhood peanut allergy: a pilot study
18. Expanded newborn screening in New South Wales: missed cases
19. 50 Years of Newborn Screening for Congenital Hypothyroidism: Current Status in Australasia and the Case for Harmonisation
20. Congenital Hypothyroid Screening Programs and the Sensitive Thyrotropin Assay: Strategies for the Surveillance of Iodine Deficiency Disorders
21. Newborn Screening for the Diagnosis and Treatment of Duchenne Muscular Dystrophy.
22. Immunoreactive Trypsinogen and Free Carnitine Changes on Newborn Screening after Birth in Patients Who Develop Type 1 Diabetes
23. Effect of Maternal Metformin Treatment in Pregnancy on Neonatal Metabolism: Evidence From Newborn Metabolic Screening
24. Healthcare Use and Costs of Medium-chain Acyl-Coa Dehydrogenase Deficiency in Australia: Screening Versus No Screening
25. Using record linkage to investigate perinatal factors and neonatal thyroid-stimulating hormone
26. Fifty years of newborn screening
27. Newborn screening for spinal muscular atrophy with disease-modifying therapies: a cost-effectiveness analysis
28. Challenges in Diagnosing Intermediate Maple Syrup Urine Disease by Newborn Screening and Functional Validation of Genomic Results Imperative for Reproductive Family Planning
29. Newborn screening for congenital hypothyroidism in very-low-birth-weight babies: the need for a second test
30. Integrating newborn screening for spinal muscular atrophy into health care systems: an Australian pilot programme.
31. Outcome of neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency in Australia: a cohort study
32. Integrating a Pilot Newborn Screening for Spinal Muscular Atrophy Into the Australian Public Healthcare System
33. Differences in Newborn Screening Results Among Women with Gestational Diabetes Mellitus
34. Maternal attitudes to newborn screening for fragile X syndrome
35. Homocysteine Measurement in Dried Blood Spot for Neonatal Detection of Homocystinurias
36. Screening newborns for inborn errors of metabolism by tandem mass spectrometry
37. Newborn Screening Samples for Diabetes Research: An Underused Resource
38. Association of elevated neonatal thyroid-stimulating hormone levels with school performance and stimulant prescription for attention deficit hyperactivity disorder in childhood
39. Evaluation of a Two-Tier Screening Pathway for Congenital Adrenal Hyperplasia in the New South Wales Newborn Screening Programme
40. 'We Needed This': Perspectives of Parents and Healthcare Professionals Involved in a Pilot Newborn Screening Program for Spinal Muscular Atrophy
41. Effect of Maternal Metformin Treatment in Pregnancy on Neonatal Metabolism: Evidence From Newborn Metabolic Screening.
42. Two-year pilot study of newborn screening for congenital adrenal hyperlasia in New South Wales compared with nationwide case surveillance in Australia
43. Newborn screening
44. Neonatal Thyrotropin as Measured in a Congenital Hypothyroidism Screening Program: Influence of the Mode of Delivery
45. Iodine status in pregnant women and their newborns: Are our babies at risk of iodine deficiency?
46. Carnitine transporter defect diagnosed by newborn screening with electrospray tandem mass spectrometry
47. Newborn screening methods for cystic fibrosis
48. Pancreatic function and extended mutation analysis in ΔF508 heterozygous infants with an elevated immunoreactive trypsinogen but normal sweat electrolyte levels
49. Screening Pathways through China, the Asia Pacific Region, the World
50. Application of tandem mass spectrometry to biochemical genetics and newborn screening
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