Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1948 1
1949 1
1950 4
1951 7
1952 3
1953 6
1954 2
1955 1
1956 6
1957 5
1958 5
1959 3
1960 1
1961 5
1962 5
1963 7
1964 5
1965 5
1966 2
1967 8
1968 6
1969 11
1970 15
1971 13
1972 8
1973 9
1974 7
1975 19
1976 17
1977 9
1978 9
1979 5
1980 17
1981 12
1982 8
1983 7
1984 11
1985 16
1986 11
1987 7
1988 12
1989 15
1990 10
1991 15
1992 13
1993 14
1994 13
1995 19
1996 13
1997 22
1998 20
1999 7
2000 6
2001 11
2002 13
2003 18
2004 8
2005 15
2006 19
2007 15
2008 14
2009 15
2010 19
2011 16
2012 14
2013 11
2014 33
2015 19
2016 18
2017 15
2018 16
2019 12
2020 13
2021 10
Text availability
Article attribute
Article type
Publication date

Search Results

761 results
Results by year
Filters applied: . Clear all
Page 1
The 2017 international classification of the Ehlers-Danlos syndromes.
Malfait F, Francomano C, Byers P, Belmont J, Berglund B, Black J, Bloom L, Bowen JM, Brady AF, Burrows NP, Castori M, Cohen H, Colombi M, Demirdas S, De Backer J, De Paepe A, Fournel-Gigleux S, Frank M, Ghali N, Giunta C, Grahame R, Hakim A, Jeunemaitre X, Johnson D, Juul-Kristensen B, Kapferer-Seebacher I, Kazkaz H, Kosho T, Lavallee ME, Levy H, Mendoza-Londono R, Pepin M, Pope FM, Reinstein E, Robert L, Rohrbach M, Sanders L, Sobey GJ, Van Damme T, Vandersteen A, van Mourik C, Voermans N, Wheeldon N, Zschocke J, Tinkle B. Malfait F, et al. Among authors: robert l. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):8-26. doi: 10.1002/ajmg.c.31552. Am J Med Genet C Semin Med Genet. 2017. PMID: 28306229
PD-1 blockade induces responses by inhibiting adaptive immune resistance.
Tumeh PC, Harview CL, Yearley JH, Shintaku IP, Taylor EJ, Robert L, Chmielowski B, Spasic M, Henry G, Ciobanu V, West AN, Carmona M, Kivork C, Seja E, Cherry G, Gutierrez AJ, Grogan TR, Mateus C, Tomasic G, Glaspy JA, Emerson RO, Robins H, Pierce RH, Elashoff DA, Robert C, Ribas A. Tumeh PC, et al. Among authors: robert l. Nature. 2014 Nov 27;515(7528):568-71. doi: 10.1038/nature13954. Nature. 2014. PMID: 25428505 Free PMC article. Clinical Trial.
Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome.
Byers PH, Belmont J, Black J, De Backer J, Frank M, Jeunemaitre X, Johnson D, Pepin M, Robert L, Sanders L, Wheeldon N. Byers PH, et al. Among authors: robert l. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):40-47. doi: 10.1002/ajmg.c.31553. Am J Med Genet C Semin Med Genet. 2017. PMID: 28306228 Review.
Longevity and aging. Mechanisms and perspectives.
Labat-Robert J, Robert L. Labat-Robert J, et al. Among authors: robert l. Pathol Biol (Paris). 2015 Dec;63(6):272-6. doi: 10.1016/j.patbio.2015.08.001. Epub 2015 Sep 26. Pathol Biol (Paris). 2015. PMID: 26416405 Review.
Cell senescence: role in aging and age-related diseases.
Campisi J, Robert L. Campisi J, et al. Among authors: robert l. Interdiscip Top Gerontol. 2014;39:45-61. doi: 10.1159/000358899. Epub 2014 May 13. Interdiscip Top Gerontol. 2014. PMID: 24862014 Free PMC article. Review.
Multi-stage Differentiation Defines Melanoma Subtypes with Differential Vulnerability to Drug-Induced Iron-Dependent Oxidative Stress.
Tsoi J, Robert L, Paraiso K, Galvan C, Sheu KM, Lay J, Wong DJL, Atefi M, Shirazi R, Wang X, Braas D, Grasso CS, Palaskas N, Ribas A, Graeber TG. Tsoi J, et al. Among authors: robert l. Cancer Cell. 2018 May 14;33(5):890-904.e5. doi: 10.1016/j.ccell.2018.03.017. Epub 2018 Apr 12. Cancer Cell. 2018. PMID: 29657129 Free PMC article.
Features of Marfan syndrome not listed in the Ghent nosology - the dark side of the disease.
von Kodolitsch Y, Demolder A, Girdauskas E, Kaemmerer H, Kornhuber K, Muino Mosquera L, Morris S, Neptune E, Pyeritz R, Rand-Hendriksen S, Rahman A, Riise N, Robert L, Staufenbiel I, Szöcs K, Vanem TT, Linke SJ, Vogler M, Yetman A, De Backer J. von Kodolitsch Y, et al. Among authors: robert l. Expert Rev Cardiovasc Ther. 2019 Dec;17(12):883-915. doi: 10.1080/14779072.2019.1704625. Expert Rev Cardiovasc Ther. 2019. PMID: 31829751 Review.
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Sifrim A, Hitz MP, Wilsdon A, Breckpot J, Turki SH, Thienpont B, McRae J, Fitzgerald TW, Singh T, Swaminathan GJ, Prigmore E, Rajan D, Abdul-Khaliq H, Banka S, Bauer UM, Bentham J, Berger F, Bhattacharya S, Bu'Lock F, Canham N, Colgiu IG, Cosgrove C, Cox H, Daehnert I, Daly A, Danesh J, Fryer A, Gewillig M, Hobson E, Hoff K, Homfray T; INTERVAL Study, Kahlert AK, Ketley A, Kramer HH, Lachlan K, Lampe AK, Louw JJ, Manickara AK, Manase D, McCarthy KP, Metcalfe K, Moore C, Newbury-Ecob R, Omer SO, Ouwehand WH, Park SM, Parker MJ, Pickardt T, Pollard MO, Robert L, Roberts DJ, Sambrook J, Setchfield K, Stiller B, Thornborough C, Toka O, Watkins H, Williams D, Wright M, Mital S, Daubeney PE, Keavney B, Goodship J; UK10K Consortium, Abu-Sulaiman RM, Klaassen S, Wright CF, Firth HV, Barrett JC, Devriendt K, FitzPatrick DR, Brook JD; Deciphering Developmental Disorders Study, Hurles ME. Sifrim A, et al. Among authors: robert l. Nat Genet. 2016 Sep;48(9):1060-5. doi: 10.1038/ng.3627. Epub 2016 Aug 1. Nat Genet. 2016. PMID: 27479907 Free PMC article.
Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection.
Renard M, Francis C, Ghosh R, Scott AF, Witmer PD, Adès LC, Andelfinger GU, Arnaud P, Boileau C, Callewaert BL, Guo D, Hanna N, Lindsay ME, Morisaki H, Morisaki T, Pachter N, Robert L, Van Laer L, Dietz HC, Loeys BL, Milewicz DM, De Backer J. Renard M, et al. Among authors: robert l. J Am Coll Cardiol. 2018 Aug 7;72(6):605-615. doi: 10.1016/j.jacc.2018.04.089. J Am Coll Cardiol. 2018. PMID: 30071989 Free PMC article.
[Introduction].
Robert L. Robert L. Pathol Biol (Paris). 2014 Apr;62(2):57. doi: 10.1016/j.patbio.2014.02.006. Epub 2014 Mar 18. Pathol Biol (Paris). 2014. PMID: 24655907 French. No abstract available.
761 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page