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

Year Number of Results
2002 1
2004 5
2005 6
2006 7
2007 3
2008 6
2009 4
2010 4
2011 5
2012 3
2013 8
2014 5
2015 3
2016 5
2017 4
2018 7
2019 7
2020 12
2021 9
2022 1
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Search Results

89 results
Results by year
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Page 1
Is it Fabry disease?
Schiffmann R, Fuller M, Clarke LA, Aerts JM. Schiffmann R, et al. Among authors: fuller m. Genet Med. 2016 Dec;18(12):1181-1185. doi: 10.1038/gim.2016.55. Epub 2016 May 19. Genet Med. 2016. PMID: 27195818 Review.
Evaluation of biomarkers for Sanfilippo syndrome.
Saville JT, Flanigan KM, Truxal KV, McBride KL, Fuller M. Saville JT, et al. Among authors: fuller m. Mol Genet Metab. 2019 Sep-Oct;128(1-2):68-74. doi: 10.1016/j.ymgme.2019.05.005. Epub 2019 May 9. Mol Genet Metab. 2019. PMID: 31104888
Immunochemistry of lysosomal storage disorders.
Parkinson-Lawrence E, Fuller M, Hopwood JJ, Meikle PJ, Brooks DA. Parkinson-Lawrence E, et al. Among authors: fuller m. Clin Chem. 2006 Sep;52(9):1660-8. doi: 10.1373/clinchem.2005.064915. Epub 2006 Jul 13. Clin Chem. 2006. PMID: 16840586 Review.
Laronidase treatment of mucopolysaccharidosis I.
Wraith EJ, Hopwood JJ, Fuller M, Meikle PJ, Brooks DA. Wraith EJ, et al. Among authors: fuller m. BioDrugs. 2005;19(1):1-7. doi: 10.2165/00063030-200519010-00001. BioDrugs. 2005. PMID: 15691212 Review.
Is it Pompe Disease? Australian diagnostic considerations.
Tchan M, Henderson R, Kornberg A, Kairaitis K, Fuller M, Davis M, Ellaway C, Reardon K, Corbett A, Needham M, McKelvie P. Tchan M, et al. Among authors: fuller m. Neuromuscul Disord. 2020 May;30(5):389-399. doi: 10.1016/j.nmd.2020.03.007. Epub 2020 Apr 16. Neuromuscul Disord. 2020. PMID: 32418839
89 results