Results 21 to 30 of about 1,668 (159)
Single coronary artery and Takayasu's arteritis: An extremely rare association
Heart India, 2017 Single coronary artery is a rare congenital anomaly of the coronary artery. The association ranges from predominantly asymptomatic to myocardial infarction, syncope being an uncommon presentation of Takayasu's arteritis.
Biswajit Majumder +4 more
doaj +1 more source
Sudden Death in a Child: The Mystery Behind the Cardiac Mass [PDF]
Journal of Clinical and Diagnostic Research, 2019 A 12-year-old boy suddenly collapsed while playing and was brought to the emergency department, where he was declared dead. The child had no prior medical illness.
Neethu Tony Mampilly +3 more
doaj +1 more source
Lack of Antilipoprotein Lipase Antibodies in Takayasu's Arteritis
Clinical and Developmental Immunology, 2009 Background. Antilipoprotein lipase (anti-LPL) antibodies were described in rheumatic diseases. In systemic lupus erythematosus they were highly associated with inflammatory markers and dyslipidemia, and may ultimately contribute to vascular damage.
Jozélio Freire de Carvalho +4 more
doaj +1 more source
Stroke as the initial presentation of Takayasu's arteritis: A case report
Radiology Case Reports, 2020 In this study, we report the case of a pediatric neurology stroke patient who was ultimately diagnosed with Takayasu's Arteritis. Our case describes a 14-year-old Hispanic female with no significant past medical history who presented to an outside ...
Paran Davari, BS +2 more
doaj +1 more source
Scientific Reports, 2022 This study aimed to evaluate the relative risk of malignancy in patients with Takayasu’s arteritis compared to that in the general population. This retrospective nationwide cohort study used data from the Korean Health Insurance Review and Assessment ...
Seulkee Lee +6 more
doaj +1 more source
Reumatismo, 2011 The discovery of Takayasu’s arteritis is likely to date back as far as 1830, owing to the first description of the Japanese Rokushu Yamamoto. Thereafter, several authors from certain geographical areas and in various historical periods described such a ...
G. Zanchin +4 more
doaj +1 more source
The genetics of Takayasu arteritis [PDF]
La Presse Médicale, 2017 Takayasu arteritis (TAK) is a rare systemic vasculitis that is characterized by granulomatous inflammation of the aorta and its major branches. The cellular and biochemical processes involved in the pathogenesis of TAK are beginning to be elucidated, and implicate both cell and antibody-mediated autoimmune mechanisms.
Paul, Renauer, Amr H, Sawalha
openaire +2 more sources
Journal of Nepal Medical Association, 2015 Takayasu’s arteritis is a well known yet rare form of large vessel vasculitis. This inflammatory disease often affects the ascending aorta and aortic arch, causing obstruction of the aorta and its major arteries. Anaesthetic management for these patients
Gentle Sunder Shrestha +3 more
doaj +3 more sources
Journal of Investigative Surgery, 2019 Objective: To analyze the clinical outcome of corticosteroid and/or immunosuppressive treatment preoperatively in patients with Takayasu's arteritis. Patients and Methods: Forty-six patients with Takayasu's arteritis who received cardiovascular surgery ...
Tie Zheng +13 more
doaj +1 more source
BMC Pulmonary Medicine, 2001 Background Takayasu's arteritis is a chronic systemic inflammatory disease that usually affects the aorta, its primary branches and occasionally the pulmonary and coronary arteries.
Bachmann Lucas M +3 more
doaj +1 more source