Boudoulas H - Search Results

1

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1.

Kass S, MacRae C, Graber HL, Sparks EA, McNamara D, Boudoulas H, Basson CT, Baker PB 3rd, Cody RJ, Fishman MC, et al. Kass S, et al. Among authors: boudoulas h. Nat Genet. 1994 Aug;7(4):546-51. doi: 10.1038/ng0894-546. Nat Genet. 1994. PMID: 7951328

2

Clinical characteristics of sudden death victims in heritable (chromosome 1p1-1q1) conduction and myocardial disease.

Nelson SD, Sparks EA, Graber HL, Boudoulas H, Mehdirad AA, Baker P, Wooley C. Nelson SD, et al. Among authors: boudoulas h. J Am Coll Cardiol. 1998 Nov 15;32(6):1717-23. doi: 10.1016/s0735-1097(98)00424-0. J Am Coll Cardiol. 1998. PMID: 9822101 Free article.

3

Heritable cardiac conduction and myocardial disease: from the clinic to the basic science laboratory and back to the clinic.

Sparks EA, Boudoulas KD, Raman SV, Sasaki T, Graber HL, Nelson SD, Seidman CE, Boudoulas H. Sparks EA, et al. Among authors: boudoulas kd, boudoulas h. Cardiology. 2011;118(3):179-86. doi: 10.1159/000328638. Epub 2011 Jun 17. Cardiology. 2011. PMID: 21691096 Free article.

4

Anti-beta-receptor antibodies in familial cardiomyopathy: correlation with HLA-DR and HLA-DQ gene polymorphisms.

Limas C, Limas CJ, Boudoulas H, Bair R, Graber H, Sparks L, Wooley CF. Limas C, et al. Among authors: boudoulas h. Am Heart J. 1994 Feb;127(2):382-6. doi: 10.1016/0002-8703(94)90128-7. Am Heart J. 1994. PMID: 7905245

5

HLA-DQA1 and -DQB1 gene haplotypes in familial cardiomyopathy.

Limas C, Limas CJ, Boudoulas H, Bair R, Sparks L, Graber H, Wooley CF. Limas C, et al. Among authors: boudoulas h. Am J Cardiol. 1994 Sep 1;74(5):510-2. doi: 10.1016/0002-9149(94)90918-0. Am J Cardiol. 1994. PMID: 8059740 No abstract available.

6

The floppy, myxomatous mitral valve, mitral valve prolapse, and mitral regurgitation.

Wooley CF, Baker PB, Kolibash AJ, Kilman JW, Sparks EA, Boudoulas H. Wooley CF, et al. Among authors: boudoulas h. Prog Cardiovasc Dis. 1991 May-Jun;33(6):397-433. doi: 10.1016/0033-0620(91)90005-7. Prog Cardiovasc Dis. 1991. PMID: 2028020 No abstract available.

7

Mitral valve prolapse and the mitral valve prolapse syndrome.

Fontana ME, Sparks EA, Boudoulas H, Wooley CF. Fontana ME, et al. Among authors: boudoulas h. Curr Probl Cardiol. 1991 May;16(5):309-75. doi: 10.1016/0146-2806(91)90022-3. Curr Probl Cardiol. 1991. PMID: 2055093 Review. No abstract available.

8

T-cell receptor gene polymorphisms in familial cardiomyopathy: correlation with anti-beta-receptor autoantibodies.

Limas C, Limas CJ, Boudoulas H, Graber H, Bair R, Sparks L, Wooley CF. Limas C, et al. Among authors: boudoulas h. Am Heart J. 1992 Nov;124(5):1258-63. doi: 10.1016/0002-8703(92)90409-o. Am Heart J. 1992. PMID: 1359779

9

Tricuspid valve disease: tricuspid valve complex perspective.

Raman SV, Sparks EA, Boudoulas H, Wooley CF. Raman SV, et al. Among authors: boudoulas h. Curr Probl Cardiol. 2002 Mar;27(3):103-42. Curr Probl Cardiol. 2002. PMID: 11979238 Review. No abstract available.

10

Left atrial performance indices in chronic mitral valve disease.

Boudoulas H, Boudoulas D, Sparks EA, Pearson AC, Nagaraja HN, Wooley CF. Boudoulas H, et al. Among authors: boudoulas d. J Heart Valve Dis. 1995 Oct;4 Suppl 2:S242-7; discussion S248. J Heart Valve Dis. 1995. PMID: 8564003

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