Results 51 to 60 of about 14,454 (200)
Takayasu's arteritis: A study of 104 Italian patients
, 2005 Takayasu's arteritis (TA) is a rare vasculitis. The Italian Takayasu's Arteritis study group was established with the aim to describe a large cohort of ...
Sabbadini, M. G +17 more
core +1 more source
Takayasu’s Arteritis Presenting as Ischemic Stroke in Young Patient
Journal of Rawalpindi Medical College, 2019 Takayasu’s arteritis is a chronic inflammatory vasculopathy. It commonly affects large blood vessels like aorta and its branches. Disease prevalence is more in women in second to third decade of life.
Sehrish Iqbal +5 more
doaj
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
Arthritis &Rheumatology, Volume 78, Issue 9, Page 1961-1974, September 2026.Objective The unknown pathophysiology and the lack of specific features for systemic juvenile idiopathic arthritis and adult‐onset Still disease (collectively known as Still disease; SD) delay diagnosis and appropriate treatment. The goal of this study was to identify features and mechanisms that distinguish SD from other systemic autoinflammatory ...
Yvonne M. Mueller +16 more
wiley +1 more source
Intracranial haemodynamics in Takayasu's arteritis
, 1992 The cerebral circulation was assessed in two cases of Takayasu's arteritis by angiography of the aortic arch, cerebral blood flow single photon emission computed tomography (SPECT) and transcranial Doppier sonography (TCD).
Grosset, D.G., Patterson, J., Bone, I.
core +1 more source
A Case Report of Takayasu’s Arteritis
Journal of Ophthalmology, 2017 Background: Takayasu’s arteritis is a non-specific autoimmune disease affecting large-size blood vessels, with a predilection for the aorta and its major branches.
O.O. Andrushkova +4 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 9, September 2026.ABSTRACT Takayasu arteritis should be suspected in young females with limb claudication, absent pulses, recurrent arterial stenosis, and elevated inflammatory markers. Early diagnosis is crucial to prevent complications. In G6PD‐deficient females, treatment must be modified, as specific immunosuppressants, like cyclophosphamide, can induce hemolysis ...
Junaid Imran +4 more
wiley +1 more source
Pulmonary artery hypertension as an initial manifestation of Takayasu's arteritis: A case report [PDF]
, 2010 Takayasu's arteritis is a rare chronic vasculitis of unknown etiology. Symptomatic pulmonary artery disease may be the first sign of Takayasu's arteritis. We describe a 51-year-old woman who presented with severe dyspnea.
Aydın Kaderli, Aysel +6 more
core +1 more source
Radiology Case Reports, 2020 Posterior Reversible Encephalopathy Syndrome (PRES) is a rare complication of Takayasu's Arteritis. A 54-year-old, right-handed woman presented with Lilliputian visual hallucinations, postprandial abdominal pain, blurred vision and headaches.
R.M. Dunne, MB, BCh, BAO +7 more
doaj +1 more source
Takayasu's arteritis: a review of the literature.
, 2006 Takayasu's arteritis is a rare, idiopathic, chronic inflammatory disease with cell-mediated inflammation, involving mainly the aorta and its major branches. It leads to stenosis, occlusion or aneurysmal degeneration of large arteries.
Michela Di Renzo +9 more
core +1 more source