Results 51 to 60 of about 14,218 (148)
Advanced Science, Volume 13, Issue 53, 24 September 2026.As a pilot phase of the Central Asian Genomic Diversity Project, whole‐genome sequencing of 166 individuals from 20 Central Asian and Afghan Hazara populations reveals fine‐scale substructure shaped by repeated trans‐Eurasian migration and admixture. Integrated analyses uncover post‐admixture adaptation, archaic introgression, and medically relevant ...
Mengge Wang +11 more
wiley +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
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
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
An Unusual Association: Takayasu’s Arteritis and Tubulointerstitial Nephritis and Uveitis Syndrome [PDF]
, 2020 The coexistence of two immune-mediated diseases in the same patient is unusual. Takayasu’s arteritis (TA), which is a chronic granulomatous vasculitis, was discovered in a 47-year-old woman followed for tubulointerstitial nephritis and ...
Derbel, Abir +3 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
Relapse of Takayasu’s arteritis with tuberculosis relapse: a rare presentation [PDF]
, 2017 Takayasu’s Arteritis (TA) is a disease of unknown etiology with incidence between 1.2 to 2.3 cases per million per year. It is a chronic granulomatous arteritis affecting large elastic arteries, predominantly the aorta, its main branches, pulmonary and ...
Gupta, Aarti Ashok +3 more
core
Takayasu’s Arteritis: An Uncommon Cause of Renal Artery Stenosis and Therapeutic Considerations
, 2013 Takayasu’s arteritis is a rare disorder characterized by granulomatous and necro-inflammatory disease of the aorta and its major branches. Its etiology remains unknown. We report a young woman with Takayasu’s arteritis affecting the aortic arch, carotid,
Vachharajani, Tushar +5 more
core +1 more source
The Turkish Journal of Gastroenterology, 2016 Takayasu’s arteritis is a chronic, non-specific primary and inflammatory disease of large vessels, especially the aorta and its branches. Although pulmonary artery involvement is common, clinical signs of pulmonary artery involvement as the initial ...
Murathan KÜÇÜK +4 more
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