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

Year Number of Results
1976 1
1977 1
1979 1
1984 1
1987 3
1988 3
1989 4
1990 4
1991 4
1992 1
1993 3
1994 5
1995 8
1996 8
1997 9
1998 5
1999 7
2000 12
2001 6
2002 7
2003 7
2004 9
2005 9
2006 7
2007 8
2008 13
2009 12
2010 7
2011 6
2012 11
2013 9
2014 16
2015 12
2016 8
2017 15
2018 19
2019 18
2020 15
2021 9
2022 10
2023 13
2024 0

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296 results

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Page 1
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 …
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/lymphangio …
We summarize the pneumothorax-associated genetic syndromes, including Birt-Hogg-Dube syndrome, Marfan syndrome, vascular
Type III collagen (COL3A1): Gene and protein structure, tissue distribution, and associated diseases.
Kuivaniemi H, Tromp G. Kuivaniemi H, et al. Gene. 2019 Jul 30;707:151-171. doi: 10.1016/j.gene.2019.05.003. Epub 2019 May 7. Gene. 2019. PMID: 31075413 Free PMC article. Review.
Type III collagen, an extracellular matrix protein, is synthesized by cells as a pre-procollagen. ...Mutations in the COL3A1 gene cause the vascular type of Ehlers-Danlos syndrome (vEDS; OMIM 130050). It is the most serious form of EDS, s
Type III collagen, an extracellular matrix protein, is synthesized by cells as a pre-procollagen. ...Mutations in the COL3A1 gene cau
[Joint hypermobility syndrome].
Carbonell-Bobadilla N, Rodríguez-Álvarez AA, Rojas-García G, Barragán-Garfias JA, Orrantia-Vertiz M, Rodríguez-Romo R. Carbonell-Bobadilla N, et al. Acta Ortop Mex. 2020 Nov-Dec;34(6):441-449. Acta Ortop Mex. 2020. PMID: 34020527 Free article. Review. Spanish.
To diagnose hypermobility syndrome, Brighton's criteria are generally accepted and published in 1998. This criteria also known as benign joint hypermobility syndrome. The term benign is used to distinguish it from other more severe conditions such as Ehler-Danlos
To diagnose hypermobility syndrome, Brighton's criteria are generally accepted and published in 1998. This criteria also known as ben …
Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome.
Byers PH, Belmont J, Black J, De Backer J, Frank M, Jeunemaitre X, Johnson D, Pepin M, Robert L, Sanders L, Wheeldon N. Byers PH, et al. Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):40-47. doi: 10.1002/ajmg.c.31553. Am J Med Genet C Semin Med Genet. 2017. PMID: 28306228 Review.
Vascular Ehlers Danlos syndrome (vEDS) is an uncommon genetic disorders characterized by arterial aneurysm, dissection and rupture, bowel rupture, and rupture of the gravid uterus. The frequency is estimated as 1/50,000-1/200,000 and results from patho
Vascular Ehlers Danlos syndrome (vEDS) is an uncommon genetic disorders characterized by arterial aneurysm, diss
Hypermobility, the Ehlers-Danlos syndromes and chronic pain.
Syx D, De Wandele I, Rombaut L, Malfait F. Syx D, et al. Clin Exp Rheumatol. 2017 Sep-Oct;35 Suppl 107(5):116-122. Epub 2017 Sep 28. Clin Exp Rheumatol. 2017. PMID: 28967365 Free article. Review.
In the absence of other conditions that cause chronic pain, these individuals are usually diagnosed with joint hypermobility syndrome (JHS). JHS is a multifactorial trait with a strong genetic basis, but no specific genetic markers. Clinical overlap of JHS is seen with her …
In the absence of other conditions that cause chronic pain, these individuals are usually diagnosed with joint hypermobility syndrome
Differential diagnosis and diagnostic flow chart of joint hypermobility syndrome/ehlers-danlos syndrome hypermobility type compared to other heritable connective tissue disorders.
Colombi M, Dordoni C, Chiarelli N, Ritelli M. Colombi M, et al. Am J Med Genet C Semin Med Genet. 2015 Mar;169C(1):6-22. doi: 10.1002/ajmg.c.31429. Am J Med Genet C Semin Med Genet. 2015. PMID: 25821090 Review.
Joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type (JHS/EDS-HT) is an evolving and protean disorder mostly recognized by generalized joint hypermobility and without a defined molecular basis. ...In this review, we revise the …
Joint hypermobility syndrome/Ehlers-Danlos syndrome hypermobility type (JHS/EDS-HT) is an evolving and pr …
Neuronal Migration Disorders.
Roberts B. Roberts B. Radiol Technol. 2018 Jan;89(3):279-295. Radiol Technol. 2018. PMID: 29298944 Review.
Magnetic resonance imaging plays a primary role in the diagnosis and classification of neuronal migration disorders. These disorders include polymicrogyria, schizencephaly, lissencephaly, heterotopia, and focal cortical dysplasia. ...
Magnetic resonance imaging plays a primary role in the diagnosis and classification of neuronal migration disorders. These disorders include …
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 …
Spontaneous gastrointestinal (GI) perforation is a well-known complication occurring in patients suffering from Type IV vas
296 results