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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1965 1
1971 1
1991 1
1992 1
1993 2
1994 1
1999 4
2000 2
2001 4
2002 1
2003 6
2005 1
2006 10
2007 4
2008 7
2009 5
2010 8
2011 11
2012 7
2013 2
2014 6
2015 1
2016 4
2017 4
2018 2
2019 7
2020 5
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Article type
Publication date

Similar Articles for PMID: 33051225

101 results
Results by year
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Page 1
Newborn Screening and Long-term Outcomes.
Powell CM. Powell CM. Pediatrics. 2020 Nov;146(5):e2020023663. doi: 10.1542/peds.2020-023663. Epub 2020 Oct 13. Pediatrics. 2020. PMID: 33051225 No abstract available.
Mountain States Genetics Regional Collaborative Center's Metabolic Newborn Screening Long-term Follow-up Study: a collaborative multi-site approach to newborn screening outcomes research.
Wright EL, Van Hove JL, Thomas J; Mountain States Metabolic Consortium. Wright EL, et al. Genet Med. 2010 Dec;12(12 Suppl):S228-41. doi: 10.1097/GIM.0b013e3181fe5d50. Genet Med. 2010. PMID: 21150369 Free article.
Long-term follow-up in newborn screening: A systems approach for improving health outcomes.
Lloyd-Puryear MA, Brower A. Lloyd-Puryear MA, et al. Genet Med. 2010 Dec;12(12 Suppl):S256-60. doi: 10.1097/GIM.0b013e3181fe5d9c. Genet Med. 2010. PMID: 21150372 Free article.
[Expert consensus on the follow-up of newborn screening for neonatal genetic and metabolic diseases].
Committee For Proficiency Testing Neonatal Genetic Metabolic Disease Screening Center National Health Commission Of China, Ou M, Jiang J, Wang Z. Committee For Proficiency Testing Neonatal Genetic Metabolic Disease Screening Center National Health Commission Of China, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Apr 10;37(4):367-372. doi: 10.3760/cma.j.issn.1003-9406.2020.04.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32219815 Chinese.
Long-term follow-up of children with confirmed newborn screening disorders using record linkage.
Wang Y, Caggana M, Sango-Jordan M, Sun M, Druschel CM. Wang Y, et al. Genet Med. 2011 Oct;13(10):881-6. doi: 10.1097/GIM.0b013e31821e485b. Genet Med. 2011. PMID: 21637103 Free article.
Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings.
Hinton CF, Mai CT, Nabukera SK, Botto LD, Feuchtbaum L, Romitti PA, Wang Y, Piper KN, Olney RS. Hinton CF, et al. Genet Med. 2014 Jun;16(6):484-90. doi: 10.1038/gim.2013.177. Epub 2013 Dec 5. Genet Med. 2014. PMID: 24310309 Free PMC article.
Newborn dried bloodspot screening: long-term follow-up activities and information system requirements.
Singh RH, Hinman AR. Singh RH, et al. Genet Med. 2010 Dec;12(12 Suppl):S261-6. doi: 10.1097/GIM.0b013e3181fe5f6c. Genet Med. 2010. PMID: 21150373 Free article.
SCREENING NEWBORNS FOR HEREDITARY METABOLIC DISEASE.
SCRIVER CR. SCRIVER CR. Pediatr Clin North Am. 1965 Aug;12:807-21. doi: 10.1016/s0031-3955(16)31746-1. Pediatr Clin North Am. 1965. PMID: 14312838 Review. No abstract available.
Newborn screening of metabolic disorders.
Arélin M, Beblo S. Arélin M, et al. J Pediatr Endocrinol Metab. 2016 Jan;29(1):1-3. doi: 10.1515/jpem-2015-0456. J Pediatr Endocrinol Metab. 2016. PMID: 26756088 Free article. No abstract available.
Follow-up status during the first 5 years of life for metabolic disorders on the federal Recommended Uniform Screening Panel.
Feuchtbaum L, Yang J, Currier R. Feuchtbaum L, et al. Genet Med. 2018 Aug;20(8):831-839. doi: 10.1038/gim.2017.199. Epub 2017 Dec 7. Genet Med. 2018. PMID: 29215646 Free article.
101 results
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