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Equine arteritis virus-infected cells contain six polyadenylated virus-specific RNAs
, 1982 M. F. van Berlo +2 more
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Acta Chirurgica Belgica, 2000
This paper reviews the literature of Takayasu's arteritis (T.A.). The concept of this disease has evolved considerably over the past decades. T.A. was first described by Mikito Takayasu in 1908, and was thought to be restricted to south-east Asia. But due to the increasing reports from all over the world, it is well established that T.A. has world-wide
Désiron Q, Zeaiter R
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This paper reviews the literature of Takayasu's arteritis (T.A.). The concept of this disease has evolved considerably over the past decades. T.A. was first described by Mikito Takayasu in 1908, and was thought to be restricted to south-east Asia. But due to the increasing reports from all over the world, it is well established that T.A. has world-wide
Désiron Q, Zeaiter R
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Takayasu's Arteritis and Temporal Arteritis
Annals of Vascular Surgery, 1992The giant cell arteritides, temporal arteritis and Takayasu’s arteritis, are granulomatous vasculitides affecting medium and large-sized arteries. Temporal arteritis is a systemic panarteritis affecting the elderly, with greater than 95% of patients being over 50 years of age, although a few case reports in young adults and adolescents exist.
L.H. Hollier, C.D. Procter
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Current Treatment Options in Cardiovascular Medicine, 2008
Takayasu's arteritis is a rare disease that causes arterial inflammation with resulting stenosis or aneurysm of affected vessels. It primarily affects young females and has a predilection for the aorta, its primary branches, and the pulmonary arteries.
Carol A. Langford, Curry L. Koening
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Takayasu's arteritis is a rare disease that causes arterial inflammation with resulting stenosis or aneurysm of affected vessels. It primarily affects young females and has a predilection for the aorta, its primary branches, and the pulmonary arteries.
Carol A. Langford, Curry L. Koening
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Clinical Rheumatology, 1994
Diagnosing Polymyalgia Rheumatica (PMR) or Giant Cell Arthritis (GCA) on an established background of arthritis is fraught with difficulties. We describe one such case.
E. George, Paul Dieppe
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Diagnosing Polymyalgia Rheumatica (PMR) or Giant Cell Arthritis (GCA) on an established background of arthritis is fraught with difficulties. We describe one such case.
E. George, Paul Dieppe
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Current Opinion in Rheumatology, 2021
Purpose of review The purpose of this review is to summarize the recent advances in Takayasu arteritis (TAK), mainly focusing on pathogenesis, imaging modalities, and management. Recent findings Three novel clusters based on angiographic findings were identified in the Indian cohort
Sinem Nihal, Esatoglu, Gulen, Hatemi
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Purpose of review The purpose of this review is to summarize the recent advances in Takayasu arteritis (TAK), mainly focusing on pathogenesis, imaging modalities, and management. Recent findings Three novel clusters based on angiographic findings were identified in the Indian cohort
Sinem Nihal, Esatoglu, Gulen, Hatemi
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The Lancet, 2000
A 66-year-old woman presented in June, 1998 with a 3week history of intermittent confusion, unsteadiness, slurred speech, and fuzzy vision. She had had mild gait unsteadiness for over 1 year and for 6 months had complained of malaise and a poor appetite with 10 kg weight loss. She had had headaches for 3 weeks before admission, which she believed was a
M. Zeidler, Tom Hughes, Adam Zeman
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A 66-year-old woman presented in June, 1998 with a 3week history of intermittent confusion, unsteadiness, slurred speech, and fuzzy vision. She had had mild gait unsteadiness for over 1 year and for 6 months had complained of malaise and a poor appetite with 10 kg weight loss. She had had headaches for 3 weeks before admission, which she believed was a
M. Zeidler, Tom Hughes, Adam Zeman
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Rheumatic Disease Clinics of North America, 1994
Takayasu's arteritis has become increasingly recognized as a worldwide entity with a variable spectrum of disease expression. Although evidence for immune mechanisms of disease exist, the precise etiopathogenesis remains elusive. Improvements in the evaluation of disease activity beyond the current parameters of clinical symptoms, erythrocyte ...
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Takayasu's arteritis has become increasingly recognized as a worldwide entity with a variable spectrum of disease expression. Although evidence for immune mechanisms of disease exist, the precise etiopathogenesis remains elusive. Improvements in the evaluation of disease activity beyond the current parameters of clinical symptoms, erythrocyte ...
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Irish Journal of Medical Science, 1981
Atheroembolism accurring spontaneously in an elderly male without an abdominal aortic aneurysm is described. Arteritis was present at the sites of impaction of the emboli. The aetiology, diagnosis and clinical presentation of this unusual form of arteritis are discussed.
E. C. Sweeney, John Sheehan
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Atheroembolism accurring spontaneously in an elderly male without an abdominal aortic aneurysm is described. Arteritis was present at the sites of impaction of the emboli. The aetiology, diagnosis and clinical presentation of this unusual form of arteritis are discussed.
E. C. Sweeney, John Sheehan
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Current Treatment Options in Cardiovascular Medicine, 1999
Takayasu's arteritis is a worldwide entity that requires astuteness for early diagnosis. The challenge for the practicing physician is to document active disease, not only to justify immunosuppressive therapy but also to determine the appropriate timing for surgical intervention.
Gail S. Kerr, Niveditha Mohan
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Takayasu's arteritis is a worldwide entity that requires astuteness for early diagnosis. The challenge for the practicing physician is to document active disease, not only to justify immunosuppressive therapy but also to determine the appropriate timing for surgical intervention.
Gail S. Kerr, Niveditha Mohan
openaire +3 more sources