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

Year Number of Results
2003 1
2005 1
2006 1
2007 1
2008 2
2010 3
2011 6
2012 2
2013 3
2014 3
2015 1
2016 2
2017 3
2018 2
2019 4
2020 6
2021 5
2022 4
2023 5
2024 2

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50 results

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Page 1
Collaborative evaluation study on 18 candidate diseases for newborn screening in 1.77 million samples.
Maier EM, Mütze U, Janzen N, Steuerwald U, Nennstiel U, Odenwald B, Schuhmann E, Lotz-Havla AS, Weiss KJ, Hammersen J, Weigel C, Thimm E, Grünert SC, Hennermann JB, Freisinger P, Krämer J, Das AM, Illsinger S, Gramer G, Fang-Hoffmann J, Garbade SF, Okun JG, Hoffmann GF, Kölker S, Röschinger W. Maier EM, et al. Among authors: janzen n. J Inherit Metab Dis. 2023 Nov;46(6):1043-1062. doi: 10.1002/jimd.12671. Epub 2023 Sep 12. J Inherit Metab Dis. 2023. PMID: 37603033
[Development of analytics in newborn screening-from the Guthrie card to genetics].
Janzen N, Sander J. Janzen N, et al. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2023 Nov;66(11):1214-1221. doi: 10.1007/s00103-023-03774-5. Epub 2023 Oct 12. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2023. PMID: 37828293 Free PMC article. Review. German.
Detection of maple toxins in mare's milk.
Sander J, Terhardt M, Janzen N. Sander J, et al. Among authors: janzen n. J Vet Intern Med. 2021 Jan;35(1):606-609. doi: 10.1111/jvim.16004. Epub 2020 Dec 18. J Vet Intern Med. 2021. PMID: 33336854 Free PMC article.
Neonatal screening for citrullinaemia.
Sander J, Janzen N, Sander S, Steuerwald U, Das AM, Scholl S, Trefz FK, Koch HG, Häberle J, Korall H, Marquardt I, Korenke C. Sander J, et al. Among authors: janzen n. Eur J Pediatr. 2003 Jun;162(6):417-20. doi: 10.1007/s00431-003-1177-z. Epub 2003 Apr 8. Eur J Pediatr. 2003. PMID: 12684898
Diagnosis of severe growth hormone deficiency in the newborn.
Binder G, Weber K, Rieflin N, Steinruck L, Blumenstock G, Janzen N, Franz AR. Binder G, et al. Among authors: janzen n. Clin Endocrinol (Oxf). 2020 Sep;93(3):305-311. doi: 10.1111/cen.14264. Epub 2020 Jun 29. Clin Endocrinol (Oxf). 2020. PMID: 32521075
A newborn screening approach to diagnose 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.
Václavík J, Mádrová L, Kouřil Š, de Sousa J, Brumarová R, Janečková H, Jáčová J, Friedecký D, Knapková M, Kluijtmans LAJ, Grünert SC, Vaz FM, Janzen N, Wanders RJA, Wevers RA, Adam T. Václavík J, et al. Among authors: janzen n. JIMD Rep. 2020 Apr 14;54(1):79-86. doi: 10.1002/jmd2.12118. eCollection 2020 Jul. JIMD Rep. 2020. PMID: 32685354 Free PMC article.
50 results