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

Year Number of Results
1993 6
1999 1
2000 1
2003 1
2006 1
2007 4
2008 1
2009 2
2010 3
2011 6
2012 5
2013 6
2014 9
2015 9
2016 11
2017 7
2018 14
2019 16
2020 21
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Similar Articles for PMID: 33051224

101 results
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Long-term Outcomes of Individuals With Metabolic Diseases Identified Through Newborn Screening.
Mütze U, Garbade SF, Gramer G, Lindner M, Freisinger P, Grünert SC, Hennermann J, Ensenauer R, Thimm E, Zirnbauer J, Leichsenring M, Gleich F, Hörster F, Grohmann-Held K, Boy N, Fang-Hoffmann J, Burgard P, Walter M, Hoffmann GF, Kölker S. Mütze U, et al. Pediatrics. 2020 Nov;146(5):e20200444. doi: 10.1542/peds.2020-0444. Epub 2020 Oct 13. Pediatrics. 2020. PMID: 33051224
Efficacy and outcome of expanded newborn screening for metabolic diseases--report of 10 years from South-West Germany.
Lindner M, Gramer G, Haege G, Fang-Hoffmann J, Schwab KO, Tacke U, Trefz FK, Mengel E, Wendel U, Leichsenring M, Burgard P, Hoffmann GF. Lindner M, et al. Orphanet J Rare Dis. 2011 Jun 20;6:44. doi: 10.1186/1750-1172-6-44. Orphanet J Rare Dis. 2011. PMID: 21689452 Free PMC article.
A Population-Based Genomic Study of Inherited Metabolic Diseases Detected Through Newborn Screening.
Park KJ, Park S, Lee E, Park JH, Park JH, Park HD, Lee SY, Kim JW. Park KJ, et al. Ann Lab Med. 2016 Nov;36(6):561-72. doi: 10.3343/alm.2016.36.6.561. Ann Lab Med. 2016. PMID: 27578510 Free PMC article.
Challenges for Worldwide Harmonization of Newborn Screening Programs.
Martínez-Morillo E, Prieto García B, Álvarez Menéndez FV. Martínez-Morillo E, et al. Clin Chem. 2016 May;62(5):689-98. doi: 10.1373/clinchem.2015.240903. Epub 2016 Mar 21. Clin Chem. 2016. PMID: 27001491 Review.
Chinese expert brief consensus on newborn screening of inherited metabolic disorders during the novel coronavirus infection epidemic.
Liu S, Wang D, Wan K, Liu H, Zhang D, Yang J, Yuan Z, He X, Wang J, Ou M, Zhu W, Qu Y, Zhao D, Wang W, Liu S, Gu M, Huang S, Wang Z, Zou L. Liu S, et al. Ann Transl Med. 2020 Apr;8(7):429. doi: 10.21037/atm.2020.03.60. Ann Transl Med. 2020. PMID: 32395473 Free PMC article. Review.
Diversity in the incidence and spectrum of organic acidemias, fatty acid oxidation disorders, and amino acid disorders in Asian countries: Selective screening vs. expanded newborn screening.
Shibata N, Hasegawa Y, Yamada K, Kobayashi H, Purevsuren J, Yang Y, Dung VC, Khanh NN, Verma IC, Bijarnia-Mahay S, Lee DH, Niu DM, Hoffmann GF, Shigematsu Y, Fukao T, Fukuda S, Taketani T, Yamaguchi S. Shibata N, et al. Mol Genet Metab Rep. 2018 May 21;16:5-10. doi: 10.1016/j.ymgmr.2018.05.003. eCollection 2018 Sep. Mol Genet Metab Rep. 2018. PMID: 29946514 Free PMC article.
Development of newborn screening connect (NBS connect): a self-reported patient registry and its role in improvement of care for patients with inherited metabolic disorders.
Osara Y, Coakley K, Devarajan A, Singh RH. Osara Y, et al. Orphanet J Rare Dis. 2017 Jul 19;12(1):132. doi: 10.1186/s13023-017-0684-3. Orphanet J Rare Dis. 2017. PMID: 28724394 Free PMC article.
Diagnostic contribution of metabolic workup for neonatal inherited metabolic disorders in the absence of expanded newborn screening.
Bower A, Imbard A, Benoist JF, Pichard S, Rigal O, Baud O, Schiff M. Bower A, et al. Sci Rep. 2019 Oct 1;9(1):14098. doi: 10.1038/s41598-019-50518-0. Sci Rep. 2019. PMID: 31575911 Free PMC article.
Newborn screening for lysosomal diseases: current status and potential interface with population medical genetics in Latin America.
Giugliani R. Giugliani R. J Inherit Metab Dis. 2012 Sep;35(5):871-7. doi: 10.1007/s10545-011-9436-z. Epub 2012 Jan 10. J Inherit Metab Dis. 2012. PMID: 22231381
Propionic acidemia: neonatal versus selective metabolic screening.
Grünert SC, Müllerleile S, de Silva L, Barth M, Walter M, Walter K, Meissner T, Lindner M, Ensenauer R, Santer R, Bodamer OA, Baumgartner MR, Brunner-Krainz M, Karall D, Haase C, Knerr I, Marquardt T, Hennermann JB, Steinfeld R, Beblo S, Koch HG, Konstantopoulou V, Scholl-Bürgi S, van Teeffelen-Heithoff A, Suormala T, Sperl W, Kraus JP, Superti-Furga A, Schwab KO, Sass JO. Grünert SC, et al. J Inherit Metab Dis. 2012 Jan;35(1):41-9. doi: 10.1007/s10545-011-9419-0. Epub 2011 Dec 2. J Inherit Metab Dis. 2012. PMID: 22134541
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