Last Posted: Jun 29, 2018
- Newborn Screening and Emerging Therapies for X-Linked Adrenoleukodystrophy
AB Moser et al, JAMA Neurology, June 25, 2018 - Updates in Newborn Screening.
Rajabi Farrah et al. Pediatric annals 2018 May 47(5) e187-e190 - Multiplex tandem mass spectrometry assay for newborn screening of X-linked adrenoleukodystrophy, biotinidase deficiency, and galactosemia with flexibility to assay other enzyme assays and biomarkers.
Hong Xinying et al. Molecular genetics and metabolism 2018 Mar - Optimizing Treatment for Cerebral Adrenoleukodystrophy in the Era of Gene Therapy.
Engelen Marc et al. The New England journal of medicine 2017 Oct (17) 1682-1684 - Hematopoietic Stem-Cell Gene Therapy for Cerebral Adrenoleukodystrophy.
Eichler Florian et al. The New England journal of medicine 2017 Oct - Newborn screening for X-linked adrenoleukodystrophy: evidence summary and advisory committee recommendation.
Kemper Alex R et al. Genetics in medicine : official journal of the American College of Medical Genetics 2016 Jun - Newborn screening for X-linked adrenoleukodystrophy: evidence summary and advisory committee recommendation
AR Kemper et al, Genetics in Medicine, June 23, 2016 - Challenges for Worldwide Harmonization of Newborn Screening Programs.
Martínez-Morillo Eduardo et al. Clinical chemistry 2016 Mar - Advisory Committee on Heritable Disorders in Newborns and Children. Secretarial Responses Regarding the Committee's Recommendations to add Adrenoleukodystrophy (X-ALD)[PDF 137 KB]
- Simultaneous quantitation of hexacosanoyl lysophosphatidylcholine, amino acids, acylcarnitines, and succinylacetone during FIA-ESI-MS/MS analysis of dried blood spot extracts for newborn screening.
Haynes Christopher A et al. Clinical biochemistry 2015 Oct
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