Cost-Effectiveness Analysis of Newborn Screening for Spinal Muscular Atrophy in Italy
Author:
Funder
Novartis Gene Therapies
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s40261-024-01386-8.pdf
Reference63 articles.
1. Burns JK, Kothary R, Parks RJ. Opening the window: The case for carrier and perinatal screening for spinal muscular atrophy. Neuromuscul Disord. 2016;26:551–9. https://doi.org/10.1016/j.nmd.2016.06.459.
2. Carré A, Empey C. Review of spinal muscular atrophy (SMA) for prenatal and pediatric genetic counselors. J Genet Couns. 2016;25:32–43. https://doi.org/10.1007/s10897-015-9859-z.
3. Farrar MA, Johnston HM, Grattan-Smith P, Turner A, Kiernan MC. Spinal muscular atrophy: molecular mechanisms. Curr Mol Med. 2009;9:851–62. https://doi.org/10.2174/156652409789105516.
4. Wirth B, Karakaya M, Kye MJ, Mendoza-Ferreira N. Twenty-five years of spinal muscular atrophy research: from phenotype to genotype to therapy, and what comes next. Annu Rev Genomics Hum Genet. 2020;21:231–61. https://doi.org/10.1146/annurev-genom-102319-103602.
5. Istituto Superiore di Sanità. Screening neonatale. 5 Jan 2022. Available at: https://www.iss.it/web/guest/screening-neonatali. Accessed 1 Apr 2024.
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