Last Posted: Nov 21, 2019
- 3-Methylcrotonyl-CoA carboxylase deficiency newborn screening in a population of 536,008: is routine screening necessary?
Wang Huaiyan et al. Journal of pediatric endocrinology & metabolism : JPEM 2019 Nov - Evaluation of earlier versus later dietary management in long-chain 3-hydroxyacyl-CoA dehydrogenase or mitochondrial trifunctional protein deficiency: a systematic review.
Fraser Hannah et al. Orphanet journal of rare diseases 2019 Nov 14(1) 258 - Newborn Screening for Mucopolysaccharidoses: Results of a Pilot Study with 100 000 Dried Blood Spots.
Scott Clifford Ronald et al. The Journal of pediatrics 2019 Nov - Variation in hospital admission of sickle cell patients from the emergency department using the Pediatric Health Information System.
Jacob Seethal A et al. Pediatric blood & cancer 2019 Nov e28067 - Public Health Perspectives on Ensuring Life Long Benefits of Newborn Screening
MJ Khoury, CDC Blog, November 18, 2019 - Expanded Newborn Screening for Inborn Errors of Metabolism by Tandem Mass Spectrometry in Suzhou, China: Disease Spectrum, Prevalence, Genetic Characteristics in a Chinese Population.
Wang Ting et al. Frontiers in genetics 2019 101052 - Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq
LF Ross et al, Pediatrics, November 2019 - Genome Sequencing in Newborns Raises Ethical Issues
NY Times, November 2019 - [Follow-up protocol of patients with cystic fibrosis diagnosed by newborn screening].
Gartner Silvia et al. Anales de pediatria (Barcelona, Spain : 2003) 2019 Apr 90(4) 251.e1-251.e10 - Inborn Errors of Metabolism: From Preconception to Adulthood.
Kruszka Paul et al. American family physician 2019 99(1) 25-32
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