Results 81 to 90 of about 3,750 (180)
A genome-wide association study identifies risk alleles in plasminogen and P4HA2 associated with giant cell arteritis [PDF]
, 2016 Giant cell arteritis (GCA) is the most common form of vasculitis in individuals older than 50 years in Western countries. To shed light onto the genetic background influencing susceptibility for GCA, we performed a genome-wide association screening in a ...
Abdel Salih +183 more
core +5 more sources
Pregnancy in Takayasu Arteritis: A Case Report of Successful Pregnancy in a Large Aortic Aneurysm
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT A 29‐year‐old primigravida woman with a gestational age of 19 weeks visited in the cardio‐obstetrics clinic for hypertension. Physical examination revealed auscultated systolic and diastolic murmurs in the second right intercostal space. Transthoracic echocardiography (TTE) showed severe left ventricle (LV) enlargement with mild systolic ...
Mona Yadollahi +5 more
wiley +1 more source
Imaging in the evaluation of renovascular disease [PDF]
, 2009 Renovascular disease (RVD) is an important cause of hypertension in children, as it often is amenable to potentially curative treatment. Imaging aimed at finding RVD therefore needs to have high sensitivity so as not to miss important findings.
Clare A. McLaren +3 more
core +2 more sources
Pharmacoepidemiology and Drug Safety, Volume 34, Issue 10, October 2025.ABSTRACT Purpose Oral glucocorticoids (OGCs) have a broad range of uses and are effective in treating numerous conditions. However, it is commonly acknowledged that OGCs at high doses or over long periods have a burden of toxicity. Despite the use of steroid‐sparing therapies, OGCs continue to be prescribed to treat a wide range of immune and ...
Elizabeth Moore +13 more
wiley +1 more source
British Journal of Haematology, Volume 207, Issue 6, Page 2648-2652, December 2025.
Guillaume Brenac +7 more
wiley +1 more source
Acute ischemic cholecystitis in Takayasu’s syndrome – a rare finding [PDF]
Archives of the Balkan Medical Union, 2018 Introduction. Takayasu’s arteritis or pulseless disease is a systemic inflammatory disease of an unknown etiology, affecting medium and large arteries and their branches, leading to stenosis, occlusions, or aneurysmal degeneration. It is more frequent in
Bogdan SOCEA +7 more
doaj
Case Reports in Rheumatology, 2013 We present a case of a 34-year-old male who presented to the emergency ward with fever and abdominal pain. The diagnosis of Takayasu’s arteritis and also antiphospholipid syndrome was made during an imaging workup of deep-vein thrombosis.
Demet Menekşe Gerede +7 more
doaj +1 more source
Journal of Medical Case Reports, 2011 Introduction The simultaneous presence of Takayasu's arteritis and beta thalassemia trait is a rare combination. To the best of our knowledge, this is the first case report on Takayasu's arteritis and beta thalassemia presenting together.
Shabbir Fahad A, Ishaq Mohammad G
doaj +1 more source
Therapeutic advances in the treatment of vasculitis [PDF]
, 2016 Considerable therapeutic advances for the treatment of vasculitis of the young have been made in the past 10 years, including the development of outcome measures that facilitate clinical trial design.
Brogan, PA, Eleftheriou, D
core +2 more sources
Re-do aortic operation in a young patient for aggressive Takayasu’s arteritis
Journal of Cardiothoracic Surgery, 2012 Takayasu’s arteritis is an inflammatory arteriopathy which involves the aorta and its major branches, causing mainly stenosis of their lumen, though aneurysmal lesions can also occur.
Bougioukas Ioannis +3 more
doaj +1 more source