Results 21 to 30 of about 3,731 (161)
Optimal management of Cogan’s syndrome: a multidisciplinary approach [PDF]
, 2017 Cogan's syndrome (CS) is a rare disorder characterized by nonsyphilitic interstitial keratitis (IK) and audio-vestibular symptoms. CS affects mainly young Caucasian adults, mostly during their first three decades of age, and may develop into typical and ...
D'Aguanno, Vittorio +3 more
core +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
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
Takayasu arteritis in childhood: retrospective experience from a tertiary referral centre in the United Kingdom. [PDF]
, 2015 Takayasu arteritis (TA) is an idiopathic large-vessel vasculitis affecting the aorta and its major branches. Although the disease rarely affects children, it does occur, even in infants.
Al-Obaidi, M +5 more
core +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
Stroke as the initial presentation of Takayasu's arteritis: A case report
Radiology Case Reports, 2020 In this study, we report the case of a pediatric neurology stroke patient who was ultimately diagnosed with Takayasu's Arteritis. Our case describes a 14-year-old Hispanic female with no significant past medical history who presented to an outside ...
Paran Davari, BS +2 more
doaj +1 more source
Pregnancy follow-up and outcome in a patient with Takayasu's arteritis [PDF]
, 2008 We describe here the pregnancy follow-up and outcome in a patient with Takayasu's arteritis, with a detailed account of the complications during gestation and delivery and the impact of the disease on the newborn's health.No presente relato, que descreve
Born, Daniel +5 more
core +3 more sources
, 2019 Table S1. Comparison of reported cohorts on c-TA after 2010 (data before 2010 are summarized by Brunner et al. [4]). Table S2. Clinical presentations of c-TA categorized by organic systems. Table S3. Comparison of demographic, clinical, laboratory, imaging, therapeutic features, and outcomes between c-TA patients hospitalized before and after 2007 ...
Fan, Luyun +12 more
openaire +1 more source
A case with late clinical presentation of Takayasu’s arteritis [PDF]
, 2014 Takayasu's arteritis also known as pulseless disease is a kind of granulomatous vasculitis that characterized large size vessels involvement with massive intimal fibrosis. It is usually occurs in female gender in middle ages. Unusual Takayasu's arteritis
Emre Demir Benli +3 more
core +1 more source