Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1988 5
1989 12
1990 8
1991 6
1992 6
1993 6
1994 6
1995 8
1996 8
1997 3
1998 5
1999 8
2000 5
2001 8
2002 6
2003 4
2004 7
2005 13
2006 9
2007 8
2008 6
2009 8
2010 12
2011 15
2012 17
2013 25
2014 8
2015 9
2016 22
2017 32
2018 28
2019 54
2020 46
2021 37
2022 38
2023 26
2024 11

Text availability

Article attribute

Article type

Publication date

Search Results

464 results

Results by year

Filters applied: . Clear all
Page 1
Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
Faughnan ME, Mager JJ, Hetts SW, Palda VA, Lang-Robertson K, Buscarini E, Deslandres E, Kasthuri RS, Lausman A, Poetker D, Ratjen F, Chesnutt MS, Clancy M, Whitehead KJ, Al-Samkari H, Chakinala M, Conrad M, Cortes D, Crocione C, Darling J, de Gussem E, Derksen C, Dupuis-Girod S, Foy P, Geisthoff U, Gossage JR, Hammill A, Heimdal K, Henderson K, Iyer VN, Kjeldsen AD, Komiyama M, Korenblatt K, McDonald J, McMahon J, McWilliams J, Meek ME, Mei-Zahav M, Olitsky S, Palmer S, Pantalone R, Piccirillo JF, Plahn B, Porteous MEM, Post MC, Radovanovic I, Rochon PJ, Rodriguez-Lopez J, Sabba C, Serra M, Shovlin C, Sprecher D, White AJ, Winship I, Zarrabeitia R. Faughnan ME, et al. Ann Intern Med. 2020 Dec 15;173(12):989-1001. doi: 10.7326/M20-1443. Epub 2020 Sep 8. Ann Intern Med. 2020. PMID: 32894695 Free article.
DESCRIPTION: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease with an estimated prevalence of 1 in 5000 that is characterized by the presence of vascular malformations (VMs). These result in chronic bleeding, acute hemorrhage, and complications …
DESCRIPTION: Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease with an estimated prevalence of 1 in 5000 that is …
Brain arteriovenous malformations: A review of natural history, pathobiology, and interventions.
Chen CJ, Ding D, Derdeyn CP, Lanzino G, Friedlander RM, Southerland AM, Lawton MT, Sheehan JP. Chen CJ, et al. Neurology. 2020 Nov 17;95(20):917-927. doi: 10.1212/WNL.0000000000010968. Epub 2020 Oct 1. Neurology. 2020. PMID: 33004601 Review.
Brain arteriovenous malformations (AVMs) are anomalous direct shunts between cerebral arteries and veins that convalesce into a vascular nidus. ...
Brain arteriovenous malformations (AVMs) are anomalous direct shunts between cerebral arteries and veins that convalesce into …
Hamartomas and malformations of the liver.
Torbenson MS. Torbenson MS. Semin Diagn Pathol. 2019 Jan;36(1):39-47. doi: 10.1053/j.semdp.2018.11.005. Epub 2018 Nov 17. Semin Diagn Pathol. 2019. PMID: 30579648 Review.
Hamartomas and malformations of the liver are rare and can lead to diagnostic challenges. ...Vascular malformations include telangiectasias, arteriovenous malformations, and hereditary lymphedema. ...
Hamartomas and malformations of the liver are rare and can lead to diagnostic challenges. ...Vascular malformations include te …
Pulmonary arteriovenous malformations.
Cartin-Ceba R, Swanson KL, Krowka MJ. Cartin-Ceba R, et al. Chest. 2013 Sep;144(3):1033-1044. doi: 10.1378/chest.12-0924. Chest. 2013. PMID: 24008954 Review.
Pulmonary arteriovenous malformations (PAVMs) are abnormal vascular structures that most often connect a pulmonary artery to a pulmonary vein, bypassing the normal pulmonary capillary bed and resulting in an intrapulmonary right-to-left shunt. ...
Pulmonary arteriovenous malformations (PAVMs) are abnormal vascular structures that most often connect a pulmonary artery to a …
Coronary Artery Fistula.
Rao SS, Agasthi P. Rao SS, et al. 2023 Jun 5. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. 2023 Jun 5. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–. PMID: 32644617 Free Books & Documents.
Coronary artery fistulas are rare defects in the coronary circulation system. They are congenital or acquired malformations in the assembly and circuitry of coronary arteries. Coronary artery fistulas can be grouped into two broad categories. Coronary-cameral fistulas are …
Coronary artery fistulas are rare defects in the coronary circulation system. They are congenital or acquired malformations in the as …
Pulmonary vascular diseases.
Cummings KW, Bhalla S. Cummings KW, et al. Clin Chest Med. 2015 Jun;36(2):235-48, viii. doi: 10.1016/j.ccm.2015.02.007. Epub 2015 Mar 26. Clin Chest Med. 2015. PMID: 26024602 Review.
Pulmonary vascular diseases encompass a large and diverse group of underlying pathologies ranging from venous thromboembolism to congenital malformations to inflammatory vasculitides. As a result, patients can present either acutely with dyspnea and chest pain or chronical …
Pulmonary vascular diseases encompass a large and diverse group of underlying pathologies ranging from venous thromboembolism to congenital …
Pure arterial malformations.
Brinjikji W, Cloft HJ, Flemming KD, Comelli S, Lanzino G. Brinjikji W, et al. J Neurosurg. 2018 Jul;129(1):91-99. doi: 10.3171/2017.2.JNS1744. Epub 2017 Sep 29. J Neurosurg. 2018. PMID: 28960150
OBJECTIVE Over the last half century, there have been isolated case reports of purely arterial malformations. In this study, the authors report a consecutive series of patients with pure arterial malformations, emphasizing the clinical and radiological features of t …
OBJECTIVE Over the last half century, there have been isolated case reports of purely arterial malformations. In this study, the auth …
ACR Appropriateness Criteria® Tinnitus: 2023 Update.
Expert Panel on Neurological Imaging; Jain V, Policeni B, Juliano AF, Adunka O, Agarwal M, Dubey P, Friedman ER, Gule-Monroe MK, Hagiwara M, Hunt CH, Lo BM, Oh ES, Rath TJ, Roberts JK, Schultz D, Taheri MR, Zander D, Burns J. Expert Panel on Neurological Imaging, et al. J Am Coll Radiol. 2023 Nov;20(11S):S574-S591. doi: 10.1016/j.jacr.2023.08.017. J Am Coll Radiol. 2023. PMID: 38040471
CTA or a combination of MR and MRA/MRV are used to evaluate arterial or venous abnormalities like dural arteriovenous fistula, arteriovenous malformation, carotid stenosis, dural sinus stenosis, and bony abnormalities like sigmoid sinus wall abnormalities in cases o …
CTA or a combination of MR and MRA/MRV are used to evaluate arterial or venous abnormalities like dural arteriovenous fistula, art
Cerebrofacial venous metameric syndrome-spectrum of imaging findings.
Brinjikji W, Nicholson P, Hilditch CA, Krings T, Pereira V, Agid R. Brinjikji W, et al. Neuroradiology. 2020 Apr;62(4):417-425. doi: 10.1007/s00234-020-02362-7. Epub 2020 Jan 14. Neuroradiology. 2020. PMID: 31932853 Review.
Cerebrofacial venous metameric syndrome (CVMS) is a complex craniofacial vascular malformation disorder in which patients have a constellation of venous vascular malformations affecting soft tissues, bone, dura, and neural structures including the eye and brain. ...However …
Cerebrofacial venous metameric syndrome (CVMS) is a complex craniofacial vascular malformation disorder in which patients have a constellati …
Endovascular treatment of spinal arteriovenous malformations.
Brinjikji W, Lanzino G. Brinjikji W, et al. Handb Clin Neurol. 2017;143:161-174. doi: 10.1016/B978-0-444-63640-9.00016-3. Handb Clin Neurol. 2017. PMID: 28552139 Review.
Spinal arteriovenous malformations (AVMs) are a rare but treatable cause of myelopathy and spinal cord hemorrhage. ...
Spinal arteriovenous malformations (AVMs) are a rare but treatable cause of myelopathy and spinal cord hemorrhage. ...
464 results