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1963 27
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1999 68
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2002 56
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2005 95
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2007 81
2008 98
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2010 99
2011 143
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Page 1
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
In 1998, Beighton published the classification of Ehlers-Danlos syndrome according to the Villefranche nosology. From the 1960s the genetic make up was identified. Management of bleeding problems associated with Ehlers-Danlos has been slow to progress. …
In 1998, Beighton published the classification of Ehlers-Danlos syndrome according to the Villefranche nosology. From the 1960 …
Ehlers-Danlos syndromes.
Ghali N, Sobey G, Burrows N. Ghali N, et al. BMJ. 2019 Sep 18;366:l4966. doi: 10.1136/bmj.l4966. BMJ. 2019. PMID: 31533917 Review. No abstract available.
[Ehlers-Danlos syndrome].
Leganger J, Søborg ML, Farholt S, Lund AM, Rosenberg J, Burcharth J. Leganger J, et al. Ugeskr Laeger. 2016 Apr 25;178(17):V01160014. Ugeskr Laeger. 2016. PMID: 27136954 Free article. Review. Danish.
Ehlers-Danlos syndrome (EDS) comprises a group of diseases characterized by connective tissue fragility. ...
Ehlers-Danlos syndrome (EDS) comprises a group of diseases characterized by connective tissue fragility. ...
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 presently availa …
It comprises Ehlers-Danlos syndrome type I and Ehlers-Danlos syndrome type II, but it is now apparent that these …
Pain in Ehlers-Danlos syndromes.
Bénistan K, Gillas F. Bénistan K, et al. Joint Bone Spine. 2020 May;87(3):199-201. doi: 10.1016/j.jbspin.2019.09.011. Epub 2019 Sep 25. Joint Bone Spine. 2020. PMID: 31562935 No abstract available.
Mouse Models of Musculocontractural Ehlers-Danlos Syndrome.
Yoshizawa T, Kosho T. Yoshizawa T, et al. Genes (Basel). 2023 Feb 8;14(2):436. doi: 10.3390/genes14020436. Genes (Basel). 2023. PMID: 36833362 Free PMC article. Review.
Musculocontractural Ehlers-Danlos syndrome (mcEDS) is a subtype of EDS caused by mutations in the gene for carbohydrate sulfotransferase 14 (CHST14) (mcEDS-CHST14) or dermatan sulfate epimerase (DSE) (mcEDS-DSE). ...
Musculocontractural Ehlers-Danlos syndrome (mcEDS) is a subtype of EDS caused by mutations in the gene for carbohydrate sulfot …
Ehlers-Danlos syndrome.
Hamel BC. Hamel BC. Neth J Med. 2004 May;62(5):140-2. Neth J Med. 2004. PMID: 15366695 Free article. No abstract available.
Ehlers-Danlos syndrome.
Pyeritz RE. Pyeritz RE. N Engl J Med. 2000 Mar 9;342(10):730-2. doi: 10.1056/NEJM200003093421009. N Engl J Med. 2000. PMID: 10706904 No abstract available.
Ehlers-Danlos syndrome.
Grahame R. Grahame R. S Afr Med J. 2016 May 25;106(6 Suppl 1):S45-6. doi: 10.7196/SAMJ.2016.v106i6.10991. S Afr Med J. 2016. PMID: 27245524
The Ehlers-Danlos syndromes (EDSs) were originally described by Ehlers in Denmark and Danlos in Paris in 1898 and 1908, respectively. ...
The Ehlers-Danlos syndromes (EDSs) were originally described by Ehlers in Denmark and Danlos in Paris in 1898 an …
Pathogenic mechanisms in genetically defined Ehlers-Danlos syndromes.
Syx D, Malfait F. Syx D, et al. Trends Mol Med. 2024 Sep;30(9):824-843. doi: 10.1016/j.molmed.2024.06.001. Epub 2024 Aug 14. Trends Mol Med. 2024. PMID: 39147618 Review.
The Ehlers-Danlos syndromes (EDS) are a group of rare heritable connective tissue disorders, common hallmarks of which are skin hyperextensibility, joint hypermobility, and generalized connective tissue fragility. ...
The Ehlers-Danlos syndromes (EDS) are a group of rare heritable connective tissue disorders, common hallmarks of which are ski …
5,587 results

Searches related to "ehlers danlos"