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

Year Number of Results
1952 2
1953 2
1956 2
1962 1
1965 2
1966 1
1967 5
1968 3
1969 9
1970 6
1971 6
1972 4
1973 4
1974 3
1975 5
1976 3
1977 8
1978 5
1979 8
1980 6
1981 6
1982 8
1983 5
1984 10
1985 13
1986 6
1987 11
1988 10
1989 13
1990 8
1991 11
1992 11
1993 14
1994 7
1995 10
1996 6
1997 11
1998 12
1999 12
2000 8
2001 18
2002 6
2003 5
2004 11
2005 21
2006 8
2007 12
2008 11
2009 14
2010 12
2011 22
2012 22
2013 14
2014 20
2015 16
2016 12
2017 19
2018 20
2019 23
2020 1
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Article type
Publication date

Search Results

543 results
Results by year
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Page 1
Hypermobile Ehlers-Danlos syndrome (a.k.a. Ehlers-Danlos syndrome Type III and Ehlers-Danlos syndrome hypermobility type): Clinical description and natural history.
Tinkle B, Castori M, Berglund B, Cohen H, Grahame R, Kazkaz H, Levy H. Tinkle B, et al. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):48-69. doi: 10.1002/ajmg.c.31538. Epub 2017 Feb 1. Am J Med Genet C Semin Med Genet. 2017. PMID: 28145611 Review.
Ehlers-Danlos syndrome--a historical review.
Parapia LA, Jackson C. Parapia LA, et al. Br J Haematol. 2008 Apr;141(1):32-5. doi: 10.1111/j.1365-2141.2008.06994.x. Br J Haematol. 2008. PMID: 18324963
The Ehlers-Danlos syndrome, a disorder with many faces.
De Paepe A, Malfait F. De Paepe A, et al. Clin Genet. 2012 Jul;82(1):1-11. doi: 10.1111/j.1399-0004.2012.01858.x. Epub 2012 Mar 15. Clin Genet. 2012. PMID: 22353005 Review.
Cardiovascular autonomic dysfunction in Ehlers-Danlos syndrome-Hypermobile type.
Hakim A, O'Callaghan C, De Wandele I, Stiles L, Pocinki A, Rowe P. Hakim A, et al. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):168-174. doi: 10.1002/ajmg.c.31543. Epub 2017 Feb 4. Am J Med Genet C Semin Med Genet. 2017. PMID: 28160388 Review.
Mast cell disorders in Ehlers-Danlos syndrome.
Seneviratne SL, Maitland A, Afrin L. Seneviratne SL, et al. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):226-236. doi: 10.1002/ajmg.c.31555. Epub 2017 Mar 6. Am J Med Genet C Semin Med Genet. 2017. PMID: 28261938 Review.
Ehlers-Danlos syndrome.
Narayanan M, Watkiss J. Narayanan M, et al. Acta Anaesthesiol Scand. 2009 Aug;53(7):971. doi: 10.1111/j.1399-6576.2009.02008.x. Acta Anaesthesiol Scand. 2009. PMID: 19604152 No abstract available.
Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndrome.
Van Damme T, Pang X, Guillemyn B, Gulberti S, Syx D, De Rycke R, Kaye O, de Die-Smulders CEM, Pfundt R, Kariminejad A, Nampoothiri S, Pierquin G, Bulk S, Larson AA, Chatfield KC, Simon M, Legrand A, Gerard M, Symoens S, Fournel-Gigleux S, Malfait F. Van Damme T, et al. Hum Mol Genet. 2018 Oct 15;27(20):3475-3487. doi: 10.1093/hmg/ddy234. Hum Mol Genet. 2018. PMID: 29931299
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