Get Aortic Dissection and Related Syndromes (Developments in PDF

By Ragavendra R. Baliga (Editor), Christoph A. Nienaber (Editor), Eric M. Isselbacher (Editor), Kim A.

ISBN-10: 038736000X

ISBN-13: 9780387360003

ISBN-10: 0387360018

ISBN-13: 9780387360010

This state-of the-art e-book is because of the the mixed efforts of members from the foreign Registry of Aortic Dissection (IRAD). it's the so much accomplished reference on aortic dissection The e-book has been divided into sections. every one bankruptcy presents a succinct assessment of the present scientific literature and comprises illustrations for additional rationalization.

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Additional resources for Aortic Dissection and Related Syndromes (Developments in Cardiovascular Medicine)

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Diagn. 26, 130–135. 110. Slonim SM, Nyman U, Semba CP, Miller DC, Mitchell RS, Dake MD (1996). Aortic dissection: percutaneous management of ischaemic complications with endovascular stents and balloon fenestration. J. Vasc. Surg. 23, 241–251; discussion 251–253. 111. Nienaber CA, Ince H, Petzsch M, et al. (2002). Endovascular treatment of thoracic aortic dissection and its variants. Acta Chir. Belg. 102, 292–298. 112. Palma JH, Marcondes de Souza JA, Alves CMR, et al. (2002). Selfexpandable aortic stentgraft for treatment of descending aortic dissections.

64, 1669–1675; discussion 1675–1677. 114. Shores J, Berger KR, Murphy ER, Pyeritz RE (1994). Progression of aortic dilatation and the benefit of long-term beta adrenergic blockade in Marfan’s-syndrome. N. Engl. J. Med. 330, 1335–1341. 115. Nienaber CA, von Kodolitsch Y (1999). Therapeutic management of patients with Marfan syndrome: focus on cardiovascular involvement. Cardiol. Rev. 7, 332–341. 116. Pereira L, Levran O, Ramirez F, et al. (1994). A molecular approach to the stratification of cardiovascular risk in families with Marfan’s syndrome.

The diagnosis of the Marfan syndrome is currently based on revised clinical criteria of the Gent nosology9 . The Gent criteria pay particular attention to genetic information like Marfan’s syndrome in kindreds of an unequivocally affected individual. Moreover, both skeletal and cardiovascular features are major (diagnostic) criteria, and Marfan’s is said to be present when four of eight typical manifestations are present. Considering, however, borderline manifestations (such as the MASS phenotype) or subtle phenotypic features (forme fruste), the molecular analysis of suspected Marfan’s syndrome and the delineation of criteria for differentiating other inherited conditions (genotypes) from a Marfan phenotype are of keen interest22–28 .

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Aortic Dissection and Related Syndromes (Developments in Cardiovascular Medicine) by Ragavendra R. Baliga (Editor), Christoph A. Nienaber (Editor), Eric M. Isselbacher (Editor), Kim A.

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