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

Year Number of Results
1972 1
1973 2
1974 1
1983 1
1984 1
1985 2
1986 4
1987 4
1988 1
1989 3
1990 7
1991 5
1992 9
1993 4
1994 5
1995 6
1996 8
1997 6
1998 2
1999 2
2000 6
2001 3
2002 4
2003 1
2004 7
2005 1
2006 3
2007 2
2008 1
2009 2
2010 4
2011 1
2012 2
2013 5
2014 4
2015 1
2017 1
2018 3
2019 2
2020 3
2021 3
2022 3
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130 results
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Page 1
Revised Recommendations for the Treatment of Infants Diagnosed with Spinal Muscular Atrophy Via Newborn Screening Who Have 4 Copies of SMN2.
Glascock J, Sampson J, Connolly AM, Darras BT, Day JW, Finkel R, Howell RR, Klinger KW, Kuntz N, Prior T, Shieh PB, Crawford TO, Kerr D, Jarecki J. Glascock J, et al. Among authors: klinger kw. J Neuromuscul Dis. 2020;7(2):97-100. doi: 10.3233/JND-190468. J Neuromuscul Dis. 2020. PMID: 32007960 Free PMC article. No abstract available.
Correction of cilia structure and function alleviates multi-organ pathology in Bardet-Biedl syndrome mice.
Husson H, Bukanov NO, Moreno S, Smith MM, Richards B, Zhu C, Picariello T, Park H, Wang B, Natoli TA, Smith LA, Zanotti S, Russo RJ, Madden SL, Klinger KW, Modur V, Ibraghimov-Beskrovnaya O. Husson H, et al. Among authors: klinger kw. Hum Mol Genet. 2020 Aug 29;29(15):2508-2522. doi: 10.1093/hmg/ddaa138. Hum Mol Genet. 2020. PMID: 32620959 Free PMC article.
The PKD1 gene product.
Harris PC, Germino G, Klinger K, Landes G, van Adelsberg J. Harris PC, et al. Among authors: klinger k. Nat Med. 1995 Jun;1(6):493. doi: 10.1038/nm0695-493a. Nat Med. 1995. PMID: 7585106 No abstract available.
130 results