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

Year Number of Results
1930 1
1937 1
1945 1
1948 2
1949 1
1951 1
1952 1
1953 4
1954 1
1955 5
1957 3
1958 2
1959 6
1960 1
1961 1
1962 5
1963 4
1964 7
1965 6
1966 4
1968 1
1969 4
1970 2
1971 2
1972 4
1973 2
1974 3
1975 1
1976 2
1977 4
1978 6
1979 5
1980 9
1981 5
1982 3
1983 8
1984 14
1985 9
1986 14
1987 7
1988 11
1989 12
1990 12
1991 8
1992 14
1993 14
1994 21
1995 10
1996 14
1997 16
1998 13
1999 13
2000 20
2001 14
2002 10
2003 15
2004 16
2005 22
2006 33
2007 34
2008 46
2009 37
2010 31
2011 30
2012 51
2013 56
2014 67
2015 62
2016 56
2017 52
2018 57
2019 73
2020 112
2021 55
Text availability
Article attribute
Article type
Publication date

Search Results

1,165 results
Results by year
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Page 1
Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease.
Kim J, Hu C, Moufawad El Achkar C, Black LE, Douville J, Larson A, Pendergast MK, Goldkind SF, Lee EA, Kuniholm A, Soucy A, Vaze J, Belur NR, Fredriksen K, Stojkovska I, Tsytsykova A, Armant M, DiDonato RL, Choi J, Cornelissen L, Pereira LM, Augustine EF, Genetti CA, Dies K, Barton B, Williams L, Goodlett BD, Riley BL, Pasternak A, Berry ER, Pflock KA, Chu S, Reed C, Tyndall K, Agrawal PB, Beggs AH, Grant PE, Urion DK, Snyder RO, Waisbren SE, Poduri A, Park PJ, Patterson A, Biffi A, Mazzulli JR, Bodamer O, Berde CB, Yu TW. Kim J, et al. Among authors: larson a. N Engl J Med. 2019 Oct 24;381(17):1644-1652. doi: 10.1056/NEJMoa1813279. Epub 2019 Oct 9. N Engl J Med. 2019. PMID: 31597037 Free PMC article.
Natural History of Slipped Capital Femoral Epiphysis.
Mathew SE, Larson AN. Mathew SE, et al. Among authors: larson an. J Pediatr Orthop. 2019 Jul;39(Issue 6, Supplement 1 Suppl 1):S23-S27. doi: 10.1097/BPO.0000000000001369. J Pediatr Orthop. 2019. PMID: 31169643 Review.
Pediatric Ankle Fractures: Concepts and Treatment Principles.
Su AW, Larson AN. Su AW, et al. Among authors: larson an. Foot Ankle Clin. 2015 Dec;20(4):705-19. doi: 10.1016/j.fcl.2015.07.004. Epub 2015 Oct 16. Foot Ankle Clin. 2015. PMID: 26589088 Free PMC article. Review.
Glutaric Acidemia Type 1.
Larson A, Goodman S. Larson A, et al. 2019 Sep 19. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. 2019 Sep 19. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2021. PMID: 31536184 Free Books & Documents. Review.
Intravenous N-acetylcysteine improves transplant-free survival in early stage non-acetaminophen acute liver failure.
Lee WM, Hynan LS, Rossaro L, Fontana RJ, Stravitz RT, Larson AM, Davern TJ 2nd, Murray NG, McCashland T, Reisch JS, Robuck PR; Acute Liver Failure Study Group. Lee WM, et al. Among authors: larson am. Gastroenterology. 2009 Sep;137(3):856-64, 864.e1. doi: 10.1053/j.gastro.2009.06.006. Epub 2009 Jun 12. Gastroenterology. 2009. PMID: 19524577 Free PMC article. Clinical Trial.
De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.
Mirzaa GM, Chong JX, Piton A, Popp B, Foss K, Guo H, Harripaul R, Xia K, Scheck J, Aldinger KA, Sajan SA, Tang S, Bonneau D, Beck A, White J, Mahida S, Harris J, Smith-Hicks C, Hoyer J, Zweier C, Reis A, Thiel CT, Jamra RA, Zeid N, Yang A, Farach LS, Walsh L, Payne K, Rohena L, Velinov M, Ziegler A, Schaefer E, Gatinois V, Geneviève D, Simon MEH, Kohler J, Rotenberg J, Wheeler P, Larson A, Ernst ME, Akman CI, Westman R, Blanchet P, Schillaci LA, Vincent-Delorme C, Gripp KW, Mattioli F, Guyader GL, Gerard B, Mathieu-Dramard M, Morin G, Sasanfar R, Ayub M, Vasli N, Yang S, Person R, Monaghan KG, Nickerson DA, van Binsbergen E, Enns GM, Dries AM, Rowe LJ, Tsai ACH, Svihovec S, Friedman J, Agha Z, Qamar R, Rodan LH, Martinez-Agosto J, Ockeloen CW, Vincent M, Sunderland WJ, Bernstein JA; Undiagnosed Diseases Network,, Eichler EE, Vincent JB; University of Washington Center for Mendelian Genomics (UW-CMG),, Bamshad MJ. Mirzaa GM, et al. Among authors: larson a. Genet Med. 2020 Mar;22(3):538-546. doi: 10.1038/s41436-019-0693-9. Epub 2019 Nov 14. Genet Med. 2020. PMID: 31723249 Free PMC article.
IRF2BPL gene mutation: Expanding on neurologic phenotypes.
Shelkowitz E, Singh JK, Larson A, Elias ER. Shelkowitz E, et al. Among authors: larson a. Am J Med Genet A. 2019 Nov;179(11):2263-2271. doi: 10.1002/ajmg.a.61328. Epub 2019 Aug 20. Am J Med Genet A. 2019. PMID: 31432588 Review.
Neurologic manifestations of Angelman syndrome.
Thibert RL, Larson AM, Hsieh DT, Raby AR, Thiele EA. Thibert RL, et al. Among authors: larson am. Pediatr Neurol. 2013 Apr;48(4):271-9. doi: 10.1016/j.pediatrneurol.2012.09.015. Pediatr Neurol. 2013. PMID: 23498559 Review.
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