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

Year Number of Results
1976 1
1979 1
1984 1
1987 3
1988 3
1989 4
1990 3
1991 3
1993 2
1994 3
1995 5
1996 5
1997 5
1998 2
1999 2
2000 5
2001 3
2002 2
2003 1
2004 2
2005 2
2006 1
2007 4
2008 4
2010 1
2011 1
2012 6
2013 3
2014 4
2015 1
2017 1
2018 2
2019 1
2020 1
2022 4
2023 6
2024 0

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93 results

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Page 1
The Genetics of Pneumothorax.
Boone PM, Scott RM, Marciniak SJ, Henske EP, Raby BA. Boone PM, et al. Am J Respir Crit Care Med. 2019 Jun 1;199(11):1344-1357. doi: 10.1164/rccm.201807-1212CI. Am J Respir Crit Care Med. 2019. PMID: 30681372 Free PMC article. Review.
We summarize the pneumothorax-associated genetic syndromes, including Birt-Hogg-Dube syndrome, Marfan syndrome, vascular (type IV) Ehlers-Danlos syndrome, alpha-1 antitrypsin deficiency, tuberous sclerosis complex/lymphangioleiomyo …
We summarize the pneumothorax-associated genetic syndromes, including Birt-Hogg-Dube syndrome, Marfan syndrome, vascular (t
Cervical Artery Dissections: Etiopathogenesis and Management.
Keser Z, Chiang CC, Benson JC, Pezzini A, Lanzino G. Keser Z, et al. Vasc Health Risk Manag. 2022 Sep 2;18:685-700. doi: 10.2147/VHRM.S362844. eCollection 2022. Vasc Health Risk Manag. 2022. PMID: 36082197 Free PMC article. Review.
The most common immediate complications related to CeAD are headache and neck pain (65-95%), TIA/ischemic stroke (>50%), and partial Horner's syndrome (25%). The prevailing hypothesis regarding the pathogenesis of sCeAD is that the underlying constitutional vessel wall …
The most common immediate complications related to CeAD are headache and neck pain (65-95%), TIA/ischemic stroke (>50%), and partial Horn …
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 …
Gastrointestinal and nutritional issues in joint hypermobility syndrome/Ehlers-Danlos syndrome, hypermobility type.
Castori M, Morlino S, Pascolini G, Blundo C, Grammatico P. Castori M, et al. Am J Med Genet C Semin Med Genet. 2015 Mar;169C(1):54-75. doi: 10.1002/ajmg.c.31431. Am J Med Genet C Semin Med Genet. 2015. PMID: 25821092 Review.
Gastrointestinal involvement is a well known complication of Ehlers-Danlos syndromes (EDSs), mainly in form of abdominal emergencies due to intestinal/abdominal vessels rupture in vascular EDS. In the last decade, a growing number of works investigated the relations …
Gastrointestinal involvement is a well known complication of Ehlers-Danlos syndromes (EDSs), mainly in form of abdominal emerg …
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 …
RECENT FINDINGS: Hereditary causes of large-artery aneurysms such as Marfan's syndrome have long been recognized; recent years have s …
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 hig
Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS),
Ehlers-Danlos syndrome type IV. Clinical and molecular aspects and guidelines for diagnosis and management.
De Paepe A. De Paepe A. Dermatology. 1994;189 Suppl 2:21-5. doi: 10.1159/000246984. Dermatology. 1994. PMID: 7841550 Review.
The clinical, biochemical and molecular characteristics of Ehlers-Danlos syndrome type IV are reviewed. The numerous clinical manifestations result from the generalized and excessive tissue fragility characteristic for this disorder. ...Clinical …
The clinical, biochemical and molecular characteristics of Ehlers-Danlos syndrome type IV are reviewed. T …
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.
The Ehlers-Danlos syndromes (EDS) are a heterogeneous group of inherited connective tissue disorders characterized clinically by skin fragility, skin hyperextensibility, joint hypermobility, and excessive bruising. ...Recent advances in the molecular analysis of EDS …
The Ehlers-Danlos syndromes (EDS) are a heterogeneous group of inherited connective tissue disorders characterized clinically …
Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield.
Bowen JM, Hernandez M, Johnson DS, Green C, Kammin T, Baker D, Keigwin S, Makino S, Taylor N, Watson O, Wheeldon NM, Sobey GJ. Bowen JM, et al. Eur J Hum Genet. 2023 Jul;31(7):749-760. doi: 10.1038/s41431-023-01343-7. Epub 2023 Mar 29. Eur J Hum Genet. 2023. PMID: 36977837 Free PMC article. Review.
The UK National Diagnostic Service for Ehlers-Danlos Syndromes (EDS) was established in 2009 for the rare types of EDS. ...
The UK National Diagnostic Service for Ehlers-Danlos Syndromes (EDS) was established in 2009 for the rare types of EDS. ...
93 results