Results 21 to 30 of about 5,210 (270)
Pyoderma Gangrenosum and Erythema Nodosum Revealing Takayasu’s Arteritis
Case Reports in Dermatology, 2016 We report a Caucasian female who presented with simultaneous erythema nodosum and pyoderma gangrenosum due to underlying Takayasu’s arteritis. Takayasu’s arteritis is a chronic large vessel vasculitis of unknown cause.
Jonas Loetscher +2 more
doaj +1 more source
Recovery from repeated sudden hearing loss in a patient with Takayasu’s arteritis treated with hyperbaric oxygen therapy: the first report in the literature [PDF]
, 2017 Hearing loss has been rarely reported in Takayasu's arteritis, presents as sudden sensorineural hearing loss and usually responds well to corticosteroid therapy.
ALTISSIMI, Giancarlo +8 more
core +3 more sources
A rare case of Takayasu’s arteritis presenting with stroke
Journal of Clinical and Scientific Research, 2017 Takayasu’s arteritis is a chronic inflammatory large vessel vasculitis of unknown aetiology that commonly affects women of child bearing age. It appears to have an acute early phase, with non- specific symptoms such as hypertension, headache, fever ...
P Siva Teja +5 more
doaj +1 more source
, 2015 The bacillus Calmette-Guérin (BCG) is a live, attenuated vaccine from Mycobacterium bovis obtained by Albert Calmette and Camille Guerin through 230 in vitro passages between 1908 and 1921.
BERNINI, Luigi +2 more
core +1 more source
Successful Pregnancy in a Patient with Takayasu’s Arteritis: a Case Report [PDF]
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum, 2007 Takayasu’s arteritis, so-called pulseless disease, is a syndrome mostly seen in young women. It is a chronic inflammatory arteritis affecting large vessels. It is associated with abnormal angiography of the upper aorta and its main branches, resulting in
Z Ebrahimi, Z Khalaji Nia
doaj +1 more source
Recurrent Vertigo: Is it Takayasu's Arteritis?
Case Reports in Vascular Medicine, 2013 Takayasu's arteritis (TA) is a chronic, idiopathic, inflammatory disease, that is more common in females and Asian countries. A 38-year-old female presented with recurrent vertigo.
Tiwari Ashutosh +6 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
PTPN22 gene polymorphism in Takayasu's arteritis [PDF]
, 2008 Objective. Takayasu's arteritis (TA) is a chronic, rare granulomatous panarteritis of unknown aetiology involving mainly the aorta and its major branches.
Akar, S. +18 more
core +2 more sources
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
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