MacRae CA - Search Results

1

Echocardiographic evaluation in asymptomatic relatives of patients with dilated cardiomyopathy reveals preclinical disease.

Mahon NG, Murphy RT, MacRae CA, Caforio AL, Elliott PM, McKenna WJ. Mahon NG, et al. Among authors: macrae ca. Ann Intern Med. 2005 Jul 19;143(2):108-15. doi: 10.7326/0003-4819-143-2-200507190-00009. Ann Intern Med. 2005. PMID: 16027452

2

Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history.

Murphy RT, Mogensen J, McGarry K, Bahl A, Evans A, Osman E, Syrris P, Gorman G, Farrell M, Holton JL, Hanna MG, Hughes S, Elliott PM, Macrae CA, McKenna WJ. Murphy RT, et al. Among authors: macrae ca. J Am Coll Cardiol. 2005 Mar 15;45(6):922-30. doi: 10.1016/j.jacc.2004.11.053. J Am Coll Cardiol. 2005. PMID: 15766830 Free article.

3

Splicing and dilated cardiomyopathy one gene to rule them all?

Macrae CA, McKenna WJ. Macrae CA, et al. J Am Coll Cardiol. 2009 Sep 1;54(10):942-3. doi: 10.1016/j.jacc.2009.06.009. J Am Coll Cardiol. 2009. PMID: 19712805 Free article. No abstract available.

4

Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.

Watkins H, Seidman CE, MacRae C, Seidman JG, McKenna W. Watkins H, et al. Br Heart J. 1992 Jan;67(1):34-8. doi: 10.1136/hrt.67.1.34. Br Heart J. 1992. PMID: 1739523 Free PMC article. Review. No abstract available.

5

Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.

Watkins H, Conner D, Thierfelder L, Jarcho JA, MacRae C, McKenna WJ, Maron BJ, Seidman JG, Seidman CE. Watkins H, et al. Nat Genet. 1995 Dec;11(4):434-7. doi: 10.1038/ng1295-434. Nat Genet. 1995. PMID: 7493025

6

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.

Thierfelder L, Watkins H, MacRae C, Lamas R, McKenna W, Vosberg HP, Seidman JG, Seidman CE. Thierfelder L, et al. Cell. 1994 Jun 3;77(5):701-12. doi: 10.1016/0092-8674(94)90054-x. Cell. 1994. PMID: 8205619

7

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

Watkins H, MacRae C, Thierfelder L, Chou YH, Frenneaux M, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Nat Genet. 1993 Apr;3(4):333-7. doi: 10.1038/ng0493-333. Nat Genet. 1993. PMID: 7981753

8

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

Thierfelder L, MacRae C, Watkins H, Tomfohrde J, Williams M, McKenna W, Bohm K, Noeske G, Schlepper M, Bowcock A, et al. Thierfelder L, et al. Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6270-4. doi: 10.1073/pnas.90.13.6270. Proc Natl Acad Sci U S A. 1993. PMID: 8327508 Free PMC article.

9

The Design of the Valsartan for Attenuating Disease Evolution in Early Sarcomeric Hypertrophic Cardiomyopathy (VANISH) Trial.

Ho CY, McMurray JJV, Cirino AL, Colan SD, Day SM, Desai AS, Lipshultz SE, MacRae CA, Shi L, Solomon SD, Orav EJ, Braunwald E; VANISH trial investigators and executive committee. Ho CY, et al. Among authors: macrae ca. Am Heart J. 2017 May;187:145-155. doi: 10.1016/j.ahj.2017.02.008. Epub 2017 Feb 16. Am Heart J. 2017. PMID: 28454798 Free PMC article. Clinical Trial.

10

The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.

Vassy JL, Christensen KD, Schonman EF, Blout CL, Robinson JO, Krier JB, Diamond PM, Lebo M, Machini K, Azzariti DR, Dukhovny D, Bates DW, MacRae CA, Murray MF, Rehm HL, McGuire AL, Green RC; MedSeq Project. Vassy JL, et al. Among authors: macrae ca. Ann Intern Med. 2017 Jun 27;167(3):159-169. doi: 10.7326/M17-0188. Print 2017 Aug 1. Ann Intern Med. 2017. PMID: 28654958 Free PMC article. Clinical Trial.

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