Taylor M - Search Results

1

Earlier diagnosis of autosomal dominant polycystic kidney disease: importance of family history and implications for cardiovascular and renal complications.

Taylor M, Johnson AM, Tison M, Fain P, Schrier RW. Taylor M, et al. Am J Kidney Dis. 2005 Sep;46(3):415-23. doi: 10.1053/j.ajkd.2005.05.029. Am J Kidney Dis. 2005. PMID: 16129202

2

Natural history of dilated cardiomyopathy due to lamin A/C gene mutations.

Taylor MR, Fain PR, Sinagra G, Robinson ML, Robertson AD, Carniel E, Di Lenarda A, Bohlmeyer TJ, Ferguson DA, Brodsky GL, Boucek MM, Lascor J, Moss AC, Li WL, Stetler GL, Muntoni F, Bristow MR, Mestroni L; Familial Dilated Cardiomyopathy Registry Research Group. Taylor MR, et al. J Am Coll Cardiol. 2003 Mar 5;41(5):771-80. doi: 10.1016/s0735-1097(02)02954-6. J Am Coll Cardiol. 2003. PMID: 12628721 Free article.

3

Modifier genes play a significant role in the phenotypic expression of PKD1.

Fain PR, McFann KK, Taylor MR, Tison M, Johnson AM, Reed B, Schrier RW. Fain PR, et al. Among authors: taylor mr. Kidney Int. 2005 Apr;67(4):1256-67. doi: 10.1111/j.1523-1755.2005.00203.x. Kidney Int. 2005. PMID: 15780078 Free article.

4

Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy.

Carniel E, Taylor MR, Sinagra G, Di Lenarda A, Ku L, Fain PR, Boucek MM, Cavanaugh J, Miocic S, Slavov D, Graw SL, Feiger J, Zhu XZ, Dao D, Ferguson DA, Bristow MR, Mestroni L. Carniel E, et al. Among authors: taylor mr. Circulation. 2005 Jul 5;112(1):54-9. doi: 10.1161/CIRCULATIONAHA.104.507699. Circulation. 2005. PMID: 15998695

5

Thymopoietin (lamina-associated polypeptide 2) gene mutation associated with dilated cardiomyopathy.

Taylor MR, Slavov D, Gajewski A, Vlcek S, Ku L, Fain PR, Carniel E, Di Lenarda A, Sinagra G, Boucek MM, Cavanaugh J, Graw SL, Ruegg P, Feiger J, Zhu X, Ferguson DA, Bristow MR, Gotzmann J, Foisner R, Mestroni L; Familial Cardiomyopathy Registry Research Group. Taylor MR, et al. Hum Mutat. 2005 Dec;26(6):566-74. doi: 10.1002/humu.20250. Hum Mutat. 2005. PMID: 16247757

6

Whole exome sequencing identifies a troponin T mutation hot spot in familial dilated cardiomyopathy.

Campbell N, Sinagra G, Jones KL, Slavov D, Gowan K, Merlo M, Carniel E, Fain PR, Aragona P, Di Lenarda A, Mestroni L, Taylor MR. Campbell N, et al. Among authors: taylor mr. PLoS One. 2013 Oct 29;8(10):e78104. doi: 10.1371/journal.pone.0078104. eCollection 2013. PLoS One. 2013. PMID: 24205113 Free PMC article.

7

[Dilated cardiomyopathy: etiology, clinical criteria for diagnosis and screening of the familial form].

Startari U, Taylor MR, Sinagra G, Di Lenarda A, Mestroni L. Startari U, et al. Ital Heart J Suppl. 2002 Apr;3(4):378-85. Ital Heart J Suppl. 2002. PMID: 12025380 Review. Italian.

8

Cardiomyopathy, familial dilated.

Taylor MR, Carniel E, Mestroni L. Taylor MR, et al. Orphanet J Rare Dis. 2006 Jul 13;1:27. doi: 10.1186/1750-1172-1-27. Orphanet J Rare Dis. 2006. PMID: 16839424 Free PMC article. Review.

9

Alterations in myocardial gene expression as a basis for cardiomyopathies and heart failure.

Taylor MR, Bristow MR. Taylor MR, et al. Novartis Found Symp. 2006;274:73-83; discussion 83-9, 152-5, 272-6. Novartis Found Symp. 2006. PMID: 17019807 Review.

10

Obesity-associated hypoventilation in hospitalized patients: prevalence, effects, and outcome.

Nowbar S, Burkart KM, Gonzales R, Fedorowicz A, Gozansky WS, Gaudio JC, Taylor MR, Zwillich CW. Nowbar S, et al. Among authors: taylor mr. Am J Med. 2004 Jan 1;116(1):1-7. doi: 10.1016/j.amjmed.2003.08.022. Am J Med. 2004. PMID: 14706658

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