Georgina Morton
506 Betula House, North Wharf Road
London, ENG W12DT, United Kingdom
London, ENG W12DT, United Kingdom
Last Updated: 09/26/2026
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Found 8 publications
Higher precision, first tier newborn screening for metachromatic leukodystrophy using 16:1-OH-sulfatide.
Journal: Molecular genetics and metabolism
Published: January 29, 2024
Improving newborn screening test performance for metachromatic leukodystrophy: Recommendation from a pre-pilot study that identified a late-infantile case for treatment.
Journal: Molecular genetics and metabolism
Published: December 13, 2023
Reply to Maase et al. Comment on "Jones et al. Application of a Novel Algorithm for Expanding Newborn Screening for Inherited Metabolic Disorders across Europe. Int. J. Neonatal Screen. 2022, 8, 20".
Journal: International journal of neonatal screening
Published: January 28, 2023
The burden of disease in metachromatic leukodystrophy: results of a caregiver survey in the UK and Republic of Ireland.
Journal: Orphanet journal of rare diseases
Published: November 15, 2022
The importance of early diagnosis and views on newborn screening in metachromatic leukodystrophy: results of a Caregiver Survey in the UK and Republic of Ireland.
Journal: Orphanet journal of rare diseases
Published: June 23, 2022
A New Approach to Objectively Evaluate Inherited Metabolic Diseases for Inclusion on Newborn Screening Programmes.
Journal: International journal of neonatal screening
Published: November 25, 2021
Application of a Novel Algorithm for Expanding Newborn Screening for Inherited Metabolic Disorders across Europe.
Journal: International journal of neonatal screening
Published: November 25, 2021
Showing 1-8 of 8
Last Updated: 09/26/2026