Marie E Faughnan
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Explore the profile of Marie E Faughnan including associated specialties, affiliations and a list of published articles.
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99
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1306
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Recent Articles
11.
Brassil M, Li Y, Ko M, Faughnan M, Prabhudesai V
BJR Case Rep
. 2023 Oct;
9(5):20230056.
PMID: 37780979
A 38-year-old male patient presenting with mild exertional dyspnea was noted to have a lingular opacity on chest radiograph. CT of the chest demonstrated an unusual complex inferior lingular vascular...
12.
Dinakaran S, Zhao H, Tang Y, Wang Z, Ruiz S, Nomura-Kitabayashi A, et al.
bioRxiv
. 2023 Sep;
PMID: 37745444
Increased endothelial cell (EC) proliferation is a hallmark of arteriovenous malformations (AVMs) in hereditary hemorrhagic telangiectasia (HHT). The underlying mechanism and disease relevance of this abnormal cell proliferative state of...
13.
Tuff-Gordon E, Faughnan M, Kim H, Lawton M, Vozoris N
ERJ Open Res
. 2023 Jul;
9(3.
PMID: 37483279
https://bit.ly/3TNLA6v.
14.
Kilian A, Latino G, White A, Ratjen F, McDonald J, Whitehead K, et al.
J Clin Med
. 2023 Apr;
12(7).
PMID: 37048789
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease characterized by the development of vascular malformations (VMs) in organs such as the brain and lungs, as well as telangiectases...
15.
Cannavicci A, Zhang Q, Faughnan M, Kutryk M
Genes (Basel)
. 2022 Apr;
13(4).
PMID: 35456471
Background: Hereditary hemorrhagic telangiectasia (HHT) is a rare, autosomal dominant genetic disorder characterized by life-threatening vascular dysplasia. Myeloid angiogenic cells (MACs), alternatively called early endothelial progenitor cells or circulating angiogenic...
16.
Ananiadis T, Faughnan M, Clark D, Prabhudesai V, Kim H, Lawton M, et al.
Ann Am Thorac Soc
. 2022 Apr;
19(8):1432-1435.
PMID: 35442860
No abstract available.
17.
Cardinell J, Ramjist J, Chen C, Shi W, Nguyen N, Yeretsian T, et al.
Sci Rep
. 2022 Feb;
12(1):1805.
PMID: 35110554
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder that causes vascular malformations throughout the body. The most prevalent and accessible of these lesions are found throughout the skin and...
18.
Parikh H, Lui E, Faughnan M, Al-Hesayen A, Segovia S, Gupta S
Trials
. 2021 Oct;
22(1):683.
PMID: 34625098
Background: The hepatopulmonary syndrome (HPS) is a pulmonary complication of liver disease found in 10 to 32% of patients with cirrhosis and is characterized by intrapulmonary vascular dilatations and abnormal...
19.
Wetzel-Strong S, Weinsheimer S, Nelson J, Pawlikowska L, Clark D, Starr M, et al.
Orphanet J Rare Dis
. 2021 Sep;
16(1):372.
PMID: 34479577
Background: Vascular malformations in the central nervous system are difficult to monitor and treat due to their inaccessible location. Angiogenic and inflammatory proteins are secreted into the bloodstream and may...
20.
Faughnan M, Mager J, Hetts S, Palda V, Ratjen F
Ann Intern Med
. 2021 Jul;
174(7):1035-1036.
PMID: 34280351
No abstract available.