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

Year Number of Results
1916 1
1919 1
1922 1
1923 1
1924 1
1925 1
1928 2
1929 1
1930 1
1932 1
1934 1
1935 1
1937 1
1938 2
1939 1
1941 1
1942 1
1943 1
1946 3
1947 3
1948 2
1949 2
1950 2
1951 2
1952 2
1954 1
1955 1
1956 1
1962 3
1963 2
1964 1
1966 6
1967 4
1968 8
1969 9
1970 4
1971 4
1972 3
1982 1
1983 3
1984 4
1985 1
1986 4
1987 5
1988 5
1989 4
1990 6
1991 9
1992 8
1993 7
1994 5
1995 4
1996 10
1997 11
1998 13
1999 18
2000 17
2001 22
2002 24
2003 15
2004 18
2005 20
2006 22
2007 34
2008 23
2009 31
2010 42
2011 38
2012 37
2013 32
2014 27
2015 26
2016 31
2017 27
2018 28
2019 28
2020 38
2021 14
Text availability
Article attribute
Article type
Publication date

Search Results

713 results
Results by year
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Page 1
[Necrotizing Fasciitis: A comprehensive review].
Carbonetti F, Carusi V, Guidi M, David V. Carbonetti F, et al. Among authors: david v. Clin Ter. 2015;166(2):e132-9. doi: 10.7417/CT.2015.1836. Clin Ter. 2015. PMID: 25945447 Review. Italian.
Holoprosencephaly.
Dubourg C, Bendavid C, Pasquier L, Henry C, Odent S, David V. Dubourg C, et al. Among authors: david v. Orphanet J Rare Dis. 2007 Feb 2;2:8. doi: 10.1186/1750-1172-2-8. Orphanet J Rare Dis. 2007. PMID: 17274816 Free PMC article. Review.
Extravasation of Noncytotoxic Drugs.
David V, Christou N, Etienne P, Almeida M, Roux A, Taibi A, Mathonnet M. David V, et al. Ann Pharmacother. 2020 Aug;54(8):804-814. doi: 10.1177/1060028020903406. Epub 2020 Feb 13. Ann Pharmacother. 2020. PMID: 32054312 Review.
Recent advances in understanding inheritance of holoprosencephaly.
Dubourg C, Kim A, Watrin E, de Tayrac M, Odent S, David V, Dupé V. Dubourg C, et al. Among authors: david v. Am J Med Genet C Semin Med Genet. 2018 Jun;178(2):258-269. doi: 10.1002/ajmg.c.31619. Epub 2018 May 22. Am J Med Genet C Semin Med Genet. 2018. PMID: 29785796 Free article. Review.
Activation of Cardiac Fibroblast Growth Factor Receptor 4 Causes Left Ventricular Hypertrophy.
Grabner A, Amaral AP, Schramm K, Singh S, Sloan A, Yanucil C, Li J, Shehadeh LA, Hare JM, David V, Martin A, Fornoni A, Di Marco GS, Kentrup D, Reuter S, Mayer AB, Pavenstädt H, Stypmann J, Kuhn C, Hille S, Frey N, Leifheit-Nestler M, Richter B, Haffner D, Abraham R, Bange J, Sperl B, Ullrich A, Brand M, Wolf M, Faul C. Grabner A, et al. Among authors: david v. Cell Metab. 2015 Dec 1;22(6):1020-32. doi: 10.1016/j.cmet.2015.09.002. Epub 2015 Oct 1. Cell Metab. 2015. PMID: 26437603 Free PMC article.
Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly.
Kim A, Savary C, Dubourg C, Carré W, Mouden C, Hamdi-Rozé H, Guyodo H, Douce JL; FREX Consortium; GoNL Consortium, Pasquier L, Flori E, Gonzales M, Bénéteau C, Boute O, Attié-Bitach T, Roume J, Goujon L, Akloul L, Odent S, Watrin E, Dupé V, de Tayrac M, David V. Kim A, et al. Among authors: david v. Brain. 2019 Jan 1;142(1):35-49. doi: 10.1093/brain/awy290. Brain. 2019. PMID: 30508070 Free article.
Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients.
Chérot E, Keren B, Dubourg C, Carré W, Fradin M, Lavillaureix A, Afenjar A, Burglen L, Whalen S, Charles P, Marey I, Heide S, Jacquette A, Heron D, Doummar D, Rodriguez D, Billette de Villemeur T, Moutard ML, Guët A, Xavier J, Périsse D, Cohen D, Demurger F, Quélin C, Depienne C, Odent S, Nava C, David V, Pasquier L, Mignot C. Chérot E, et al. Among authors: david v. Clin Genet. 2018 Mar;93(3):567-576. doi: 10.1111/cge.13102. Epub 2017 Oct 4. Clin Genet. 2018. PMID: 28708303 Free article.
713 results
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