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Takayasu Arteritis [PDF]

open access: yesFrontiers in Pediatrics, 2018
Takayasu arteritis is an idiopathic granulomatous vasculitis of the aorta and its main branches and it constitutes one of the more common vasculitides in children.
Ricardo A. G. Russo, María M. Katsicas
doaj   +3 more sources

Cannabis arteritis

open access: yesThe Pan African Medical Journal, 2017
Cannabis is the most consumed psychoactive substance by young people. Chronic use of cannabis can lead to cannabis arteritis, which is a very rare peripheral vascular disease similar to Buerger's disease.
Naoual El Omri   +6 more
doaj   +3 more sources

2022 American College of Rheumatology/EULAR classification criteria for Takayasu arteritis

open access: yesAnnals of the Rheumatic Diseases, 2022
To develop and validate new classification criteria for Takayasu arteritis (TAK).
P. Grayson   +12 more
semanticscholar   +2 more sources

2021 American College of Rheumatology/Vasculitis Foundation Guideline for the Management of Giant Cell Arteritis and Takayasu Arteritis

open access: yesArthritis & Rheumatology, 2021
To provide evidence‐based recommendations and expert guidance for the management of giant cell arteritis (GCA) and Takayasu arteritis (TAK) as exemplars of large vessel vasculitis.
M. Maz   +31 more
semanticscholar   +1 more source

Takayasu's disease presenting with tubercular empyema: A rare presentation of a rare disease

open access: yesJournal of the Scientific Society, 2023
Takayasu's disease (TD) also known as pulseless disease is an arteriopathy characterized by vasculitis affecting the aorta and its branches. It is also known as aortic arch syndrome, nonspecific aorto-arteritis, and young female arteritis.
Neha Gajanan Phate   +4 more
doaj   +1 more source

Clinical Characteristics and Outcomes of Aortic Arch Emergencies: Takayasu Disease, Fibromuscular Dysplasia, and Aortic Arch Pathologies: A Retrospective Study and Review of the Literature

open access: yesBiomedicines, 2023
Non-atherosclerotic aortic arch pathologies (NA-AAPs) and anatomical variants are characterized as rare cardiovascular diseases with a low incidence rate, below 1 case per 2000 population, but enormous heterogeneity in terms of anatomical variants, i.e.,
Magdalena Wawak   +7 more
doaj   +1 more source

Efficacy and safety of mavrilimumab in giant cell arteritis: a phase 2, randomised, double-blind, placebo-controlled trial

open access: yesAnnals of the Rheumatic Diseases, 2022
Objectives Granulocyte-macrophage colony-stimulating factor (GM-CSF) is implicated in pathogenesis of giant cell arteritis. We evaluated the efficacy of the GM-CSF receptor antagonist mavrilimumab in maintaining disease remission.
M. Cid   +15 more
semanticscholar   +1 more source

Roles of selenoprotein S in reactive oxygen species-dependent neutrophil extracellular trap formation induced by selenium-deficient arteritis

open access: yesRedox Biology, 2021
Selenium (Se) deficiency and poor plasma Se levels can cause cardiovascular diseases by decreasing selenoprotein levels. Neutrophil extracellular traps (NETs) may be the vicious cycle center of inflammation in vasculitis. Here, we show that Se deficiency
Qianru Chi   +5 more
semanticscholar   +1 more source

Reversible hypertension and infective arteritis

open access: yesHeart India, 2022
Background: Idiopathic vasculitides or arteritis have very few or none treatment options. Identification of infective arteritis based on high clinical suspicion opens a window for treatment of such cases . Although these are occasional clinical scenario.
Amita Diwaker   +3 more
doaj   +1 more source

SARS-CoV-2-Associated Obliterative Arteritis Causing Massive Testicular Infarction

open access: yesClinics and Practice, 2021
A 26-year-old man with symptomatic SARS-CoV-2 infection developed a sudden-onset acute testicular pain. The echo-doppler images showed massive testicular infarction, so orchiectomy was performed.
Dámaso Parrón   +6 more
doaj   +1 more source

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