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

Year Number of Results
1949 1
1950 1
1951 1
1953 1
1960 1
1961 2
1962 1
1967 1
1972 1
1977 1
1980 1
1981 1
1983 1
1989 1
1990 2
1991 2
1994 1
1998 1
2000 2
2001 2
2002 1
2003 2
2004 7
2005 7
2006 2
2007 3
2008 3
2009 3
2010 3
2011 2
2012 1
2013 1
2015 5
2016 12
2017 4
2018 3
2019 9
2020 3
2021 3
2022 1
2023 1
2024 1

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89 results

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Page 1
OPTN/SRTR 2021 Annual Data Report: Kidney.
Lentine KL, Smith JM, Miller JM, Bradbrook K, Larkin L, Weiss S, Handarova DK, Temple K, Israni AK, Snyder JJ. Lentine KL, et al. Among authors: temple k. Am J Transplant. 2023 Feb;23(2 Suppl 1):S21-S120. doi: 10.1016/j.ajt.2023.02.004. Am J Transplant. 2023. PMID: 37132350 Free PMC article.
Parent-mediated communication-focused treatment in children with autism (PACT): a randomised controlled trial.
Green J, Charman T, McConachie H, Aldred C, Slonims V, Howlin P, Le Couteur A, Leadbitter K, Hudry K, Byford S, Barrett B, Temple K, Macdonald W, Pickles A; PACT Consortium. Green J, et al. Among authors: temple k. Lancet. 2010 Jun 19;375(9732):2152-60. doi: 10.1016/S0140-6736(10)60587-9. Epub 2010 May 20. Lancet. 2010. PMID: 20494434 Free PMC article. Clinical Trial.
OPTN/SRTR 2022 Annual Data Report: Kidney.
Lentine KL, Smith JM, Lyden GR, Miller JM, Dolan TG, Bradbrook K, Larkin L, Temple K, Handarova DK, Weiss S, Israni AK, Snyder JJ. Lentine KL, et al. Among authors: temple k. Am J Transplant. 2024 Feb;24(2S1):S19-S118. doi: 10.1016/j.ajt.2024.01.012. Am J Transplant. 2024. PMID: 38431360
Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counseling.
Eggermann T, Brioude F, Russo S, Lombardi MP, Bliek J, Maher ER, Larizza L, Prawitt D, Netchine I, Gonzales M, Grønskov K, Tümer Z, Monk D, Mannens M, Chrzanowska K, Walasek MK, Begemann M, Soellner L, Eggermann K, Tenorio J, Nevado J, Moore GE, Mackay DJ, Temple K, Gillessen-Kaesbach G, Ogata T, Weksberg R, Algar E, Lapunzina P. Eggermann T, et al. Among authors: temple k. Eur J Hum Genet. 2016 Jun;24(6):784-93. doi: 10.1038/ejhg.2015.224. Epub 2015 Oct 28. Eur J Hum Genet. 2016. PMID: 26508573 Free PMC article. Review.
A case of atelosteogenesis.
Temple K, Hall CA, Chitty L, Baraitser M. Temple K, et al. J Med Genet. 1990 Mar;27(3):194-7. doi: 10.1136/jmg.27.3.194. J Med Genet. 1990. PMID: 2325095 Free PMC article.
The iris in Williams syndrome.
Holmström G, Almond G, Temple K, Taylor D, Baraitser M. Holmström G, et al. Among authors: temple k. Arch Dis Child. 1990 Sep;65(9):987-9. doi: 10.1136/adc.65.9.987. Arch Dis Child. 1990. PMID: 2221973 Free PMC article.
Discovery of structurally distinct tricyclic M4 positive allosteric modulator (PAM) chemotypes - Part 2.
Long MF, Capstick RA, Spearing PK, Engers JL, Gregro AR, Bollinger SR, Chang S, Luscombe VB, Rodriguez AL, Cho HP, Niswender CM, Bridges TM, Conn PJ, Lindsley CW, Engers DW, Temple KJ. Long MF, et al. Among authors: temple kj. Bioorg Med Chem Lett. 2021 Dec 1;53:128416. doi: 10.1016/j.bmcl.2021.128416. Epub 2021 Oct 26. Bioorg Med Chem Lett. 2021. PMID: 34710625 Free PMC article.
89 results