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Year Number of Results
1968 1
1970 1
1973 1
1975 3
1978 1
1979 2
1980 3
1981 5
1982 1
1983 5
1984 2
1985 2
1986 2
1987 6
1988 6
1989 5
1990 7
1991 9
1992 6
1993 4
1994 12
1995 9
1996 12
1997 13
1998 9
1999 12
2000 13
2001 10
2002 13
2003 12
2004 20
2005 23
2006 21
2007 22
2008 22
2009 24
2010 25
2011 29
2012 41
2013 46
2014 53
2015 39
2016 49
2017 50
2018 57
2019 85
2020 89
2021 86
2022 83
2023 67
2024 35

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992 results

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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. 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
The Ehlers-Danlos syndromes.
Malfait F, Castori M, Francomano CA, Giunta C, Kosho T, Byers PH. Malfait F, et al. Nat Rev Dis Primers. 2020 Jul 30;6(1):64. doi: 10.1038/s41572-020-0194-9. Nat Rev Dis Primers. 2020. PMID: 32732924 Review.
Ehlers-Danlos Syndrome in Pregnancy: A Review.
Kang J, Hanif M, Mirza E, Jaleel S. Kang J, et al. Eur J Obstet Gynecol Reprod Biol. 2020 Dec;255:118-123. doi: 10.1016/j.ejogrb.2020.10.033. Epub 2020 Oct 17. Eur J Obstet Gynecol Reprod Biol. 2020. PMID: 33113401 Review.
Ehlers-Danlos syndrome (EDS) is a group of connective tissue disorders that can result in a range of complications during pregnancy. ...
Ehlers-Danlos syndrome (EDS) is a group of connective tissue disorders that can result in a range of complications duri …
The evidence-based rationale for physical therapy treatment of children, adolescents, and adults diagnosed with joint hypermobility syndrome/hypermobile Ehlers Danlos syndrome.
Engelbert RH, Juul-Kristensen B, Pacey V, de Wandele I, Smeenk S, Woinarosky N, Sabo S, Scheper MC, Russek L, Simmonds JV. Engelbert RH, et al. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):158-167. doi: 10.1002/ajmg.c.31545. Am J Med Genet C Semin Med Genet. 2017. PMID: 28306230 Free article.
New insights into the phenotype of Joint Hypermobility Syndrome (JHS) and Ehlers-Danlos Syndrome-hypermobile type (hEDS) have raised many issues in relation to classification, diagnosis, assessment, and treatment. ...
New insights into the phenotype of Joint Hypermobility Syndrome (JHS) and Ehlers-Danlos Syndrome-hypermobile type (hEDS …
Physical therapy treatment of hypermobile Ehlers-Danlos syndrome: A systematic review.
Reychler G, De Backer MM, Piraux E, Poncin W, Caty G. Reychler G, et al. Am J Med Genet A. 2021 Oct;185(10):2986-2994. doi: 10.1002/ajmg.a.62393. Epub 2021 Jun 19. Am J Med Genet A. 2021. PMID: 34145717
Physiotherapy techniques are regularly prescribed in the hypermobile type Ehlers-Danlos syndrome (hEDS) and they are appreciated by the patients. ...
Physiotherapy techniques are regularly prescribed in the hypermobile type Ehlers-Danlos syndrome (hEDS) and they are ap …
A novel therapeutic strategy for Ehlers-Danlos syndrome based on nutritional supplements.
Mantle D, Wilkins RM, Preedy V. Mantle D, et al. Med Hypotheses. 2005;64(2):279-83. doi: 10.1016/j.mehy.2004.07.023. Med Hypotheses. 2005. PMID: 15607555
Ehlers-Danlos syndrome is a rare disorder, comprising a group of related inherited disorders of connective tissue, resulting from underlying abnormalities in the synthesis and metabolism of collagen. This proposal is specifically concerned with Ehlers- …
Ehlers-Danlos syndrome is a rare disorder, comprising a group of related inherited disorders of connective tissue, resu …
Acute aortic dissection: pathogenesis, risk factors and diagnosis.
Gawinecka J, Schönrath F, von Eckardstein A. Gawinecka J, et al. Swiss Med Wkly. 2017 Aug 25;147:w14489. doi: 10.4414/smw.2017.14489. eCollection 2017. Swiss Med Wkly. 2017. PMID: 28871571 Free article. Review.
However, patients with genetic connective tissue disorders such as Marfan, Loeys Dietz or Ehlers Danlos syndrome, and patients with bicuspid aortic valves are at the increased risk of aortic dissection at a much younger age. ...
However, patients with genetic connective tissue disorders such as Marfan, Loeys Dietz or Ehlers Danlos syndrome, and p …
Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type.
Malfait F, Wenstrup RJ, De Paepe A. Malfait F, et al. Genet Med. 2010 Oct;12(10):597-605. doi: 10.1097/GIM.0b013e3181eed412. Genet Med. 2010. PMID: 20847697 Free article. Review.
It comprises Ehlers-Danlos syndrome type I and Ehlers-Danlos syndrome type II, but it is now apparent that these form a continuum of clinical findings and differ only in phenotypic severity. ...No treatment for the underlying defect is pr …
It comprises Ehlers-Danlos syndrome type I and Ehlers-Danlos syndrome type II, but it is now appar …
992 results