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You searched for: Author/Creator Pyeritz, Reed

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1. Aortic Disease Presentation and Outcome Associated With ACTA2 Mutations. (June 2015)

2. Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations. (October 2018)

4. Features of Marfan syndrome not listed in the Ghent nosology – the dark side of the disease. (2nd December 2019)

5. International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium). (December 2016)

6. Recurrent Aortic Dissection: Observations From the International Registry of Aortic Dissection. Issue 14 (4th October 2016)

7. The IGNITE network: a model for genomic medicine implementation and research. Issue 1 (December 2015)