Judge DP - Search Results

1

Familial hypertrophic cardiomyopathy associated with cardiac beta-myosin heavy chain and troponin I mutations.

Frazier A, Judge DP, Schulman SP, Johnson N, Holmes KW, Murphy AM. Frazier A, et al. Among authors: judge dp. Pediatr Cardiol. 2008 Jul;29(4):846-50. doi: 10.1007/s00246-007-9177-9. Epub 2008 Jan 4. Pediatr Cardiol. 2008. PMID: 18175163

2

Penetrance of mutations in plakophilin-2 among families with arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Dalal D, James C, Devanagondi R, Tichnell C, Tucker A, Prakasa K, Spevak PJ, Bluemke DA, Abraham T, Russell SD, Calkins H, Judge DP. Dalal D, et al. Among authors: judge dp. J Am Coll Cardiol. 2006 Oct 3;48(7):1416-24. doi: 10.1016/j.jacc.2006.06.045. Epub 2006 Sep 12. J Am Coll Cardiol. 2006. PMID: 17010805 Free article.

3

Heart failure and genomics.

Judge DP, Johnson NM, Cirino AL, Ho CY. Judge DP, et al. J Am Coll Cardiol. 2007 Mar 13;49(10):1106; author reply 1106-7. doi: 10.1016/j.jacc.2006.12.020. Epub 2007 Feb 23. J Am Coll Cardiol. 2007. PMID: 17349893 Free article. No abstract available.

4

Morphologic variants of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy a genetics-magnetic resonance imaging correlation study.

Dalal D, Tandri H, Judge DP, Amat N, Macedo R, Jain R, Tichnell C, Daly A, James C, Russell SD, Abraham T, Bluemke DA, Calkins H. Dalal D, et al. Among authors: judge dp. J Am Coll Cardiol. 2009 Apr 14;53(15):1289-99. doi: 10.1016/j.jacc.2008.12.045. J Am Coll Cardiol. 2009. PMID: 19358943 Free article.

5

Use of genetics in the clinical evaluation of cardiomyopathy.

Judge DP. Judge DP. JAMA. 2009 Dec 9;302(22):2471-6. doi: 10.1001/jama.2009.1787. JAMA. 2009. PMID: 19996403

6

Genetic evaluation of familial cardiomyopathy.

Judge DP, Johnson NM. Judge DP, et al. J Cardiovasc Transl Res. 2008 Jun;1(2):144-54. doi: 10.1007/s12265-008-9025-1. Epub 2008 Apr 22. J Cardiovasc Transl Res. 2008. PMID: 20559909 Review.

7

The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance.

Noureldin RA, Liu S, Nacif MS, Judge DP, Halushka MK, Abraham TP, Ho C, Bluemke DA. Noureldin RA, et al. Among authors: judge dp. J Cardiovasc Magn Reson. 2012 Feb 20;14(1):17. doi: 10.1186/1532-429X-14-17. J Cardiovasc Magn Reson. 2012. PMID: 22348519 Free PMC article. Review.

8

Genetic testing for dilated cardiomyopathy in clinical practice.

Lakdawala NK, Funke BH, Baxter S, Cirino AL, Roberts AE, Judge DP, Johnson N, Mendelsohn NJ, Morel C, Care M, Chung WK, Jones C, Psychogios A, Duffy E, Rehm HL, White E, Seidman JG, Seidman CE, Ho CY. Lakdawala NK, et al. Among authors: judge dp. J Card Fail. 2012 Apr;18(4):296-303. doi: 10.1016/j.cardfail.2012.01.013. Epub 2012 Feb 15. J Card Fail. 2012. PMID: 22464770 Free PMC article.

9

Novel and highly lethal NKX2.5 missense mutation in a family with sudden death and ventricular arrhythmia.

Perera JL, Johnson NM, Judge DP, Crosson JE. Perera JL, et al. Among authors: judge dp. Pediatr Cardiol. 2014 Oct;35(7):1206-12. doi: 10.1007/s00246-014-0917-3. Epub 2014 Jun 1. Pediatr Cardiol. 2014. PMID: 24880466

10

A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndrome.

Doyle JJ, Doyle AJ, Wilson NK, Habashi JP, Bedja D, Whitworth RE, Lindsay ME, Schoenhoff F, Myers L, Huso N, Bachir S, Squires O, Rusholme B, Ehsan H, Huso D, Thomas CJ, Caulfield MJ, Van Eyk JE, Judge DP, Dietz HC; GenTAC Registry Consortium; MIBAVA Leducq Consortium. Doyle JJ, et al. Among authors: judge dp. Elife. 2015 Oct 27;4:e08648. doi: 10.7554/eLife.08648. Elife. 2015. PMID: 26506064 Free PMC article.

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