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

Year Number of Results
2002 10
2003 12
2004 17
2005 18
2006 18
2007 9
2008 9
2009 3
2010 13
2011 10
2012 5
2013 3
2014 6
2015 9
2016 9
2017 7
2018 5
2019 1
2020 2
2021 1
2022 1
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2024 1

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Page 1
Is SGSH heterozygosity a risk factor for early-onset neurodegenerative disease?
Douglass ML, Beard H, Shoubridge A, Nazri N, King B, Trim PJ, Duplock SK, Snel MF, Hopwood JJ, Hemsley KM. Douglass ML, et al. Among authors: hopwood jj. J Inherit Metab Dis. 2021 May;44(3):763-776. doi: 10.1002/jimd.12359. Epub 2021 Jan 25. J Inherit Metab Dis. 2021. PMID: 33423317
A Comparative Effectiveness Study of Newborn Screening Methods for Four Lysosomal Storage Disorders.
Sanders KA, Gavrilov DK, Oglesbee D, Raymond KM, Tortorelli S, Hopwood JJ, Lorey F, Majumdar R, Kroll CA, McDonald AM, Lacey JM, Turgeon CT, Tucker JN, Tang H, Currier R, Isaya G, Rinaldo P, Matern D. Sanders KA, et al. Among authors: hopwood jj. Int J Neonatal Screen. 2020 Jun;6(2):44. doi: 10.3390/ijns6020044. Epub 2020 May 30. Int J Neonatal Screen. 2020. PMID: 32802993 Free PMC article.
148 results