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Year Number of Results
1975 1
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1980 6
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1988 14
1989 18
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614 results

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Page 1
Survival is affected by mutation type and molecular mechanism in vascular Ehlers-Danlos syndrome (EDS type IV).
Pepin MG, Schwarze U, Rice KM, Liu M, Leistritz D, Byers PH. Pepin MG, et al. Genet Med. 2014 Dec;16(12):881-8. doi: 10.1038/gim.2014.72. Epub 2014 Jun 12. Genet Med. 2014. PMID: 24922459 Free article.
PURPOSE: We sought to characterize the natural history of vascular Ehlers-Danlos syndrome in individuals with heterozygous COL3A1 mutations. ...Median survival was 51 years but was influenced by gender (lower in men) and by the type of mutation. CONCLU …
PURPOSE: We sought to characterize the natural history of vascular Ehlers-Danlos syndrome in individuals with heterozyg …
Vasculitis mimics.
Molloy ES, Langford CA. Molloy ES, et al. Curr Opin Rheumatol. 2008 Jan;20(1):29-34. doi: 10.1097/BOR.0b013e3282f1dcf2. Curr Opin Rheumatol. 2008. PMID: 18281854 Review.
RECENT FINDINGS: Hereditary causes of large-artery aneurysms such as Marfan's syndrome have long been recognized; recent years have seen a greater understanding of the genetics of Marfan's and other such disorders, including Loeys-Dietz syndrome and Ehler-Danlos syndrome type
RECENT FINDINGS: Hereditary causes of large-artery aneurysms such as Marfan's syndrome have long been recognized; recent years have seen a g …
Vascular Ehlers-Danlos syndrome.
Germain DP, Herrera-Guzman Y. Germain DP, et al. Ann Genet. 2004 Jan-Mar;47(1):1-9. doi: 10.1016/j.anngen.2003.07.002. Ann Genet. 2004. PMID: 15127738 Review.
Vascular Ehlers-Danlos syndrome, also known as Ehlers-Danlos syndrome type IV, is a life-threatening inherited disorder of connective tissue, resulting from mutations in the COL3A1 gene coding for type III procollagen …
Vascular Ehlers-Danlos syndrome, also known as Ehlers-Danlos syndrome type IV, is a …
Ehlers-Danlos syndrome type IV.
Germain DP. Germain DP. Orphanet J Rare Dis. 2007 Jul 19;2:32. doi: 10.1186/1750-1172-2-32. Orphanet J Rare Dis. 2007. PMID: 17640391 Free PMC article. Review.
Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible su
Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherite
Bowel perforation in type IV vascular Ehlers-Danlos syndrome. A systematic review.
El Masri H, Loong TH, Meurette G, Podevin J, Zinzindohoue F, Lehur PA. El Masri H, et al. Tech Coloproctol. 2018 May;22(5):333-341. doi: 10.1007/s10151-018-1783-4. Epub 2018 Apr 26. Tech Coloproctol. 2018. PMID: 29700641 Review.
Spontaneous gastrointestinal (GI) perforation is a well-known complication occurring in patients suffering from Type IV vascular Ehlers-Danlos syndrome (EDS IV). The aim of the present study was to review the current literature on spontan …
Spontaneous gastrointestinal (GI) perforation is a well-known complication occurring in patients suffering from Type IV vascul …
The Ehlers-Danlos syndromes.
Yeowell HN, Pinnell SR. Yeowell HN, et al. Semin Dermatol. 1993 Sep;12(3):229-40. Semin Dermatol. 1993. PMID: 8217561 Review.
Recent advances in the molecular analysis of EDS have identified defects responsible for EDS IV (mutations in the type III collagen gene), EDS VI (homozygous and compound heterozygous mutations in the lysyl hydroxylase gene), EDS VIIA and VIIB (mutations in the t
Recent advances in the molecular analysis of EDS have identified defects responsible for EDS IV (mutations in the type III col …
The dysmorphic phenotype in vascular Ehlers Danlos syndrome.
Lyness JR, Morrison PJ. Lyness JR, et al. Clin Dysmorphol. 2023 Jan 1;32(1):1-6. doi: 10.1097/MCD.0000000000000437. Epub 2022 Nov 3. Clin Dysmorphol. 2023. PMID: 36503916 Review.
The Ehlers Danlos syndromes are identified by their connective tissue features and are not rich in dysmorphic handles. Vascular Ehlers Danlos syndrome (vEDS) however, is characterised by a recognisable phenotypic constellation of internal and external dysmorp …
The Ehlers Danlos syndromes are identified by their connective tissue features and are not rich in dysmorphic handles. Vascular Ehlers
Stroke in vascular Ehlers-Danlos syndrome.
Ranzani Martins R, da Silva Paiva ML, da Silva Teixeira WC, Kawahira RSH, Freua F, Castro MAA, Kim CA, Kok F. Ranzani Martins R, et al. Pract Neurol. 2023 Oct;23(5):436-438. doi: 10.1136/pn-2023-003753. Epub 2023 Jul 17. Pract Neurol. 2023. PMID: 37460211 No abstract available.
Vascular type of Ehlers-Danlos syndrome.
Watanabe A, Shimada T. Watanabe A, et al. J Nippon Med Sch. 2008 Oct;75(5):254-61. doi: 10.1272/jnms.75.254. J Nippon Med Sch. 2008. PMID: 19023163 Free article. Review.
Vascular type of Ehlers-Danlos syndrome (EDS), also known as EDS type IV (NIM#130050) is a life-threatening autosomal dominant inherited disorder of connective tissue, caused by mutations of the COL3A1 gene. ...
Vascular type of Ehlers-Danlos syndrome (EDS), also known as EDS type IV (NIM#130050) is a life-th …
614 results