Results 11 to 20 of about 24,513 (213)

Takayasu arteritis in children [PDF]

Pediatric Rheumatology, 2008
Abstract Takayasu arteritis (TA) is a large vessel vasculitis that usually affects young female patients during the second and third decades of life, but has been reported in children as young as 24 months of age. Aim of this report was to describe four children (two girls) with TA, as well as summarizing main published studies.
DÜZOVA, ALİ, Ekim, Mesiha, Ozen, Seza, Uncu, Nermin, Bircan, Zelal, Bayazit, Aysun Karabay, Fitoz, Suat, Soylu, Alper, BEK, KENAN, Baskin, Esra, Oner, Ayse, Sirin, Aydan, ÇALIŞKAN, Salim, Yalcinkaya, Fatos, Cakar, Nilgun   +14 more
core   +12 more sources

Takayasu Arteritis [PDF]

Frontiers in Pediatrics, 2018
La arteritis de Takayasu es una vasculitis granulomatosa idiopática de la aorta y sus ramas principales. Es más frecuente entre los asiáticos y las mujeres, y constituye una de las vasculitis más comunes en los niños. La inflamación y la proliferación de la íntima conducen al engrosamiento de la pared, lesiones estenóticas u oclusivas y trombosis ...
Ricardo Russo, María M. Katsicas
openaire   +4 more sources

Takayasu arteritis in pregnancy: A case series [PDF]

Perspectives In Medical Research, 2020
Takayasu arteritis is a disease of unknown etiology which is a primary systemic vasculitis leading to stenotic and occlusive changes. Takayasu arteritis is a chronic inflammatory disease in progressive pattern which chiefly affects the aorta and its ...
Ipsita Mohapatra1 , Subha Ranjan Samantaray1 ,G Priyanka2 , Achanta Vivekananda1
doaj   +3 more sources

Takayasu Arteritis in a G6PD Deficient Female Patient With Recurrent Axillary Artery Stenosis: A Case Report. [PDF]

Clin Case Rep
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 ...
Imran J, Rehman MZ, Osama M, Khan S, Thada PK.   +4 more
europepmc   +2 more sources

Comment on "Takayasu Arteritis and Giant Cell Arteritis: Results From a Cross-Sectional Study of 96 Italian Patients". [PDF]

Immun Inflamm Dis
Immunity, Inflammation and Disease, Volume 14, Issue 9, September 2026.
Mohanty S, Lakra AJ, Mantravadi HB, Uniyal P, Dedeepya D.   +4 more
europepmc   +2 more sources

Atherosclerosis in Takayasu arteritis [PDF]

Annals of the Rheumatic Diseases, 2006
Chronic inflammatory diseases such as systemic lupus erythematosus (SLE) and rheumatoid arthritis are associated with accelerated atherosclerosis. We hypothesised that atherosclerosis may also be increased in Takayasu arteritis.The frequency of atherosclerotic plaques and the intima-media thickness (IMT) were investigated in 30 female patients with ...
Seyahi, E, Ugurlu, S, Cumali, R, Seyahi, N, Balci, H, Fresko, I, Yurdakul, S   +6 more
openaire   +4 more sources

Takayasu arteritis in pregnancy [PDF]

Medical Journal Armed Forces India, 2015
In 1908, Mikito Takayasu, a Japanese ophthalmologist, reported the case of a 21-year-old woman with retinal arteriovenous anastomoses, syncope, and absent upper extremity pulses.1 Takayasu arteritis (TA), also known as occlusive thromboaortopathy, is a primary systemic vasculitis of unknown etiology, predominantly affecting women2 during their ...
Madhusudan, Dey, Anupam, Kapur, S, Goyal, R D, Wadhwa, A, Srivastava, R, Agarwal   +5 more
openaire   +4 more sources

Altered MicroRNA Signatures in Circulating Extracellular Vesicles Reflect Aortic Dilation in Takayasu Arteritis. [PDF]

J Extracell Biol
ABSTRACT Takayasu arteritis (TAK) is a large‐vessel vasculitis that can lead to aneurysmal dilation, yet reliable circulating biomarkers for vascular remodelling remain lacking. Extracellular vesicles (EVs) carry miRNAs implicated in vascular biology, but their relevance to TAK has not been fully explored. Circulating EVs were isolated from serum of 54
Kawajiri K, Nakagama S, Sasano T, Maejima Y.   +3 more
europepmc   +2 more sources

Malignant Ischemic Stroke in a Young Female: A Rare Primary Manifestation of Takayasu Arteritis

Case Reports in Neurological Medicine, 2019
Takayasu arteritis is a rare chronic progressive granulomatous necrotizing large vessel panvasculitis mainly involving aorta and its main branches. It commonly affects the female in second to third decades.
Bhupendra Shah, Roshan Chhetri
doaj   +2 more sources

Takayasu arteritis in Turkey

International Journal of Cardiology, 1996
Takayasu arteritis is a non-specific inflammatory process of unknown etiology affecting the aorta and its branches. A retrospective study was done in 14 patients diagnosed as Takayasu arteritis. Eleven patients were female and three were male. Ages ranged from 12 to 30 years.
Turkoglu, C, Memis, A, Payzin, S, Akin, M, Kultusay, H, Akilli, A, Can, L, Altintig, A   +7 more
openaire   +5 more sources