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Literature DB >> 27393688

Thoracic aortic dissection and heritability: forensic implications.

Elizabeth N Robertson^1,2, Brett D Hambly³, Richmond W Jeremy⁴.

Abstract

Mesh：

Year: 2016 PMID： 27393688 DOI： 10.1007/s12024-016-9788-7

Source DB: PubMed Journal: Forensic Sci Med Pathol ISSN： 1547-769X Impact factor: 2.007

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11 in total

1. 2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the diagnosis and management of patients with thoracic aortic disease. A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Thoracic Surgery, American College of Radiology,American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons,and Society for Vascular Medicine.

Authors: Loren F Hiratzka; George L Bakris; Joshua A Beckman; Robert M Bersin; Vincent F Carr; Donald E Casey; Kim A Eagle; Luke K Hermann; Eric M Isselbacher; Ella A Kazerooni; Nicholas T Kouchoukos; Bruce W Lytle; Dianna M Milewicz; David L Reich; Souvik Sen; Julie A Shinn; Lars G Svensson; David M Williams
Journal: J Am Coll Cardiol Date: 2010-04-06 Impact factor: 24.094

2. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.

Authors: Bart L Loeys; Junji Chen; Enid R Neptune; Daniel P Judge; Megan Podowski; Tammy Holm; Jennifer Meyers; Carmen C Leitch; Nicholas Katsanis; Neda Sharifi; F Lauren Xu; Loretha A Myers; Philip J Spevak; Duke E Cameron; Julie De Backer; Jan Hellemans; Yan Chen; Elaine C Davis; Catherine L Webb; Wolfram Kress; Paul Coucke; Daniel B Rifkin; Anne M De Paepe; Harry C Dietz
Journal: Nat Genet Date: 2005-01-30 Impact factor: 38.330

3. The genetic and molecular basis of bicuspid aortic valve associated thoracic aortopathy: a link to phenotype heterogeneity.

Authors: Ratnasari Padang; Paul G Bannon; Richmond Jeremy; David R Richmond; Christopher Semsarian; Michael Vallely; Michael Wilson; Tristan D Yan
Journal: Ann Cardiothorac Surg Date: 2013-01

Review 4. Perturbations of mechanotransduction and aneurysm formation in heritable aortopathies.

Authors: Richmond W Jeremy; Elizabeth Robertson; Yaxin Lu; Brett D Hambly
Journal: Int J Cardiol Date: 2013-08-27 Impact factor: 4.164

5. Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK).

Authors: P Beighton; A De Paepe; B Steinmann; P Tsipouras; R J Wenstrup
Journal: Am J Med Genet Date: 1998-04-28

6. The revised Ghent nosology for the Marfan syndrome.

Authors: Bart L Loeys; Harry C Dietz; Alan C Braverman; Bert L Callewaert; Julie De Backer; Richard B Devereux; Yvonne Hilhorst-Hofstee; Guillaume Jondeau; Laurence Faivre; Dianna M Milewicz; Reed E Pyeritz; Paul D Sponseller; Paul Wordsworth; Anne M De Paepe
Journal: J Med Genet Date: 2010-07 Impact factor: 6.318

7. Aggressive cardiovascular phenotype of aneurysms-osteoarthritis syndrome caused by pathogenic SMAD3 variants.

Authors: Denise van der Linde; Ingrid M B H van de Laar; Aida M Bertoli-Avella; Rogier A Oldenburg; Jos A Bekkers; Francesco U S Mattace-Raso; Anton H van den Meiracker; Adriaan Moelker; Fop van Kooten; Ingrid M E Frohn-Mulder; Janneke Timmermans; Els Moltzer; Jan M Cobben; Lut van Laer; Bart Loeys; Julie De Backer; Paul J Coucke; Anne De Paepe; Yvonne Hilhorst-Hofstee; Marja W Wessels; Jolien W Roos-Hesselink
Journal: J Am Coll Cardiol Date: 2012-05-23 Impact factor: 24.094

Thoracic aortic dissection and heritability: forensic implications.

2. A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.

3. The genetic and molecular basis of bicuspid aortic valve associated thoracic aortopathy: a link to phenotype heterogeneity.

Review 4. Perturbations of mechanotransduction and aneurysm formation in heritable aortopathies.

5. Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK).

6. The revised Ghent nosology for the Marfan syndrome.

7. Aggressive cardiovascular phenotype of aneurysms-osteoarthritis syndrome caused by pathogenic SMAD3 variants.

8. Aortic root dilatation in young men with normally functioning bicuspid aortic valves.

9. Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections.

10. TGF-beta in the pathogenesis and prevention of disease: a matter of aneurysmic proportions.

1. Heritability of haemodynamics in the ascending aorta.