- 新生儿遗传代谢病筛查
- 赵正言 顾学范
- 338字
- 2020-08-29 06:03:16
参考文献
1. 顾学范. 新生儿疾病筛查. 上海:上海科学技术文献出版社,2003.
2. Lee B,Scaglia F. Inborn Errors of Metabolism. //Sutton VR,Graham BH. Newborn Screening for Inborn Errors of Metabolism;New York:Oxford University Press,2015:1-34.
3. Mak CM,Lee HC,Chan AY,et al. Inborn errors of metabolism and expanded newborn screening:review and update. Crit Rev Clin Lab Sci,2013,50(6):142-162.
4. Gu XF,Ye J,Han LS,et al. Neonatal Screening for Inborn Errors of Metabolism in Shanghai. Clin Pediatr,2009,27(2):101-105.
5. Lindner M,Gramer G,Haege G,et al. Efficacy and outcome of expanded newborn screening for metabolic diseases-Report of 10 years from South-West Germany. Orphanet J Rare Dis,2011,6:44.
6. Therrell BL,Padilla CD,Loeber JG,et al. Current status of newborn screening worldwide:2015. Semin Perinatol,2015,39(3):171-187.
7. Fernhoff PM. Newborn screening for genetic disorders. Pediatr Clin North Am,2009,56(3):505-513.
8. Copeland S. A review of newborn screening in the era of tandem mass spectrometry:what’s new for the pediatric neurologist?Semin Pediatr Neurol,2008,15(3):110-116.
9. Arn PH. Newborn screening:current status. Health Aff(Millwood),2007,26(2):559-566.
10. Watson MS. Current status of newborn screening:decision-making about the conditions to include in screening programs. Ment Retard Dev Disabil Res Rev,2006,12(4):230-235.
11. Carreiro-Lewandowski E. Newborn screening:an overview. Clin Lab Sci,2002,15(4):229-238.