Results 271 to 280 of about 89,678 (332)
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IgG4-aortitis among thoracic aortic aneurysms

Heart, 2019
Objective The incidence of aortitis in patients with thoracic aortic diseases is not well established. The aim of this study was to analyse the frequency and clinical course of patients with aortitis in a surgical series. Methods 320 consecutive patients
C. Pérez-García   +12 more
semanticscholar   +1 more source

Aortic Arch Syndrome Secondary to Radiation in Childhood

Archives of Internal Medicine, 1969
A 38-year-old woman with aortic arch syndrome (pulseless disease), had received an excessive amount of radiation to her neck in early childhood. The roentgenographic, surgical, and pathologic changes found were occlusions and severe luminal narrowing of the involved arteries of the upper part of the thorax and marked artherosclerotic changes with ...
Charles Botstein   +4 more
openaire   +3 more sources

Anxiety Symptoms of the Patients With Aortic Arch Syndrome

Psychiatry and Clinical Neurosciences, 1978
We reported six cases of the aortic arch syndrome with brain symptoms. Two could be explained directly as an organic impairment of the brain. In the remaining four cases, however, the mental symptoms were considered to have a basis of "anxiety." They were easily precipitated by iatrogenic and other various environmental factors.
Saburo Otsuki   +3 more
openaire   +3 more sources

Management of the aortic arch in patients with Loeys–Dietz syndrome

The Journal of Thoracic and Cardiovascular Surgery, 2020
We sought to develop strategies for management of the aortic arch in patients with Loeys-Dietz syndrome (LDS) through a review of our clinical experience with these patients and a comparison with our experience in patients with Marfan syndrome (MFS).We reviewed hospital and follow-up records of 79 patients with LDS and compared them with 256 patients ...
J. Magruder   +11 more
openaire   +3 more sources

CLINICOPATHOLOGIC STUDIES OF A CASE OF AORTIC ARCH SYNDROME

Retina, 1986
The clinicopathologic features of a 62-year-old woman with the aortic arch syndrome who presented with ischemic ocular inflammation, followed by complete loss of vision, is presented. The pathophysiology and ocular manifestations of chronic ocular ischemia are discussed.
W. Richard Green   +2 more
openaire   +3 more sources

Genetic disorders of cardiac morphogenesis. The DiGeorge and velocardiofacial syndromes.

Circulation Research, 1997
The phenotype associated with a 22q11 deletion is highly variable and still under investigation. Of particular interest to cardiologists and cardiac developmental biologists is the finding that many patients with a 22q11 deletion have conotruncal cardiac
E. Goldmuntz, B. Emanuel
semanticscholar   +1 more source

Aortic Arch Syndrome

A.M.A. Archives of Internal Medicine, 1959
In recent years the syndrome of occlusive disease of the major vessels of the aortic arch has appeared with great frequency in the medical literature.1-8We wish to add the following case, which is unusual because of its surgical complication. Report of Case This was the fourth Coral Gables Veterans Administration Hospital admission for this 46-year ...
Paul L. Rodensky, Fred Wasserman
openaire   +3 more sources

Polymyalgia rheumatica and giant-cell arteritis.

New England Journal of Medicine, 1978
Polymyalgia rheumatica and giant-cell arteritis are closely related disorders that aff ect people of middle age and older. They frequently occur together.
C. Salvarani   +3 more
semanticscholar   +1 more source

Ortner's syndrome associated with aortic arch aneurysm

Clinical Research in Cardiology, 2007
Tascanov, Mustafa Begenc/0000-0002-9008-6631 WOS: 000243766600009 PubMed: 17252183 …
Gulel, O.   +3 more
openaire   +3 more sources

Double Aortic Arch: An Unreported Anomaly with Kabuki Syndrome [PDF]

open access: possiblePediatric Cardiology, 2008
Kabuki syndrome is a rare congenital disorder characterized by mental retardation, postnatal dwarfism, visceral anomalies, and peculiar facies (resembling the makeup of actors in Kabuki, traditional Japanese theater) initially described in Japan. Congenital heart and great vessel defects are the most frequent visceral anomalies found in children with ...
S Moral   +2 more
openaire   +2 more sources

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