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

Year Number of Results
1992 1
1997 1
1998 1
2007 1
2008 1
2011 1
2012 1
2013 1
2014 2
2015 1
2016 1
2017 3
2022 0
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12 results
Results by year
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Page 1
Fabry disease in infancy and early childhood: a systematic literature review.
Laney DA, Peck DS, Atherton AM, Manwaring LP, Christensen KM, Shankar SP, Grange DK, Wilcox WR, Hopkin RJ. Laney DA, et al. Among authors: atherton am. Genet Med. 2015 May;17(5):323-30. doi: 10.1038/gim.2014.120. Epub 2014 Sep 18. Genet Med. 2015. PMID: 25232851 Free article. Review.
HSP and deafness: Neurocristopathy caused by a novel mosaic SOX10 mutation.
Donkervoort S, Bharucha-Goebel D, Yun P, Hu Y, Mohassel P, Hoke A, Zein WM, Ezzo D, Atherton AM, Modrcin AC, Dasouki M, Foley AR, Bönnemann CG. Donkervoort S, et al. Among authors: atherton am. Neurol Genet. 2017 May 15;3(3):e151. doi: 10.1212/NXG.0000000000000151. eCollection 2017 Jun. Neurol Genet. 2017. PMID: 28534044 Free PMC article.
Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.
Soden SE, Saunders CJ, Willig LK, Farrow EG, Smith LD, Petrikin JE, LePichon JB, Miller NA, Thiffault I, Dinwiddie DL, Twist G, Noll A, Heese BA, Zellmer L, Atherton AM, Abdelmoity AT, Safina N, Nyp SS, Zuccarelli B, Larson IA, Modrcin A, Herd S, Creed M, Ye Z, Yuan X, Brodsky RA, Kingsmore SF. Soden SE, et al. Among authors: atherton am. Sci Transl Med. 2014 Dec 3;6(265):265ra168. doi: 10.1126/scitranslmed.3010076. Sci Transl Med. 2014. PMID: 25473036 Free PMC article.
Ashkenazi Jewish genetic disease carrier screening.
Begleiter ML, Buchholz JL, Atherton AM, Mays LZ, Lund MM, Strenk ME. Begleiter ML, et al. Among authors: atherton am. Genet Med. 2008 Jun;10(6):461; author reply 461-2. doi: 10.1097/gim.0b013e318170f87e. Genet Med. 2008. PMID: 18496229 No abstract available.
Peak serum bupivacaine concentration.
Atherton AM. Atherton AM. Br J Anaesth. 1992 May;68(5):540. doi: 10.1093/bja/68.5.540-b. Br J Anaesth. 1992. PMID: 1642949 No abstract available.
Maternal serum screening and 22q11.2 deletion syndrome.
Begleiter ML, Lund MM, Atherton AM, Buchholz JD, Ardinger HH. Begleiter ML, et al. Among authors: atherton am. Am J Med Genet A. 2007 Feb 15;143(4):410-1. doi: 10.1002/ajmg.a.31616. Am J Med Genet A. 2007. PMID: 17230492 No abstract available.
12 results