Ware SM - Search Results

1

Lee TM, Hsu DT, Kantor P, Towbin JA, Ware SM, Colan SD, Chung WK, Jefferies JL, Rossano JW, Castleberry CD, Addonizio LJ, Lal AK, Lamour JM, Miller EM, Thrush PT, Czachor JD, Razoky H, Hill A, Lipshultz SE. Lee TM, et al. Among authors: ware sm. Circ Res. 2017 Sep 15;121(7):855-873. doi: 10.1161/CIRCRESAHA.116.309386. Circ Res. 2017. PMID: 28912187 Free PMC article. Review.

2

Molecular genetics of heterotaxy syndromes.

Belmont JW, Mohapatra B, Towbin JA, Ware SM. Belmont JW, et al. Among authors: ware sm. Curr Opin Cardiol. 2004 May;19(3):216-20. doi: 10.1097/00001573-200405000-00005. Curr Opin Cardiol. 2004. PMID: 15096953 Review.

3

Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease.

Scaglia F, Towbin JA, Craigen WJ, Belmont JW, Smith EO, Neish SR, Ware SM, Hunter JV, Fernbach SD, Vladutiu GD, Wong LJ, Vogel H. Scaglia F, et al. Among authors: ware sm. Pediatrics. 2004 Oct;114(4):925-31. doi: 10.1542/peds.2004-0718. Pediatrics. 2004. PMID: 15466086

4

Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy.

Jefferies JL, Eidem BW, Belmont JW, Craigen WJ, Ware SM, Fernbach SD, Neish SR, Smith EO, Towbin JA. Jefferies JL, et al. Among authors: ware sm. Circulation. 2005 Nov 1;112(18):2799-804. doi: 10.1161/CIRCULATIONAHA.104.528281. Epub 2005 Oct 24. Circulation. 2005. PMID: 16246949

5

Pediatric restrictive cardiomyopathy associated with a mutation in beta-myosin heavy chain.

Ware SM, Quinn ME, Ballard ET, Miller E, Uzark K, Spicer RL. Ware SM, et al. Clin Genet. 2008 Feb;73(2):165-70. doi: 10.1111/j.1399-0004.2007.00939.x. Epub 2007 Dec 12. Clin Genet. 2008. PMID: 18076673

6

Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.

Mohapatra B, Casey B, Li H, Ho-Dawson T, Smith L, Fernbach SD, Molinari L, Niesh SR, Jefferies JL, Craigen WJ, Towbin JA, Belmont JW, Ware SM. Mohapatra B, et al. Among authors: ware sm. Hum Mol Genet. 2009 Mar 1;18(5):861-71. doi: 10.1093/hmg/ddn411. Epub 2008 Dec 8. Hum Mol Genet. 2009. PMID: 19064609 Free PMC article.

7

High resolution SNP based microarray mapping of mosaic supernumerary marker chromosomes 13 and 17: delineating novel loci for apraxia.

Kogan JM, Miller E, Ware SM. Kogan JM, et al. Among authors: ware sm. Am J Med Genet A. 2009 May;149A(5):887-93. doi: 10.1002/ajmg.a.32750. Am J Med Genet A. 2009. PMID: 19353585

8

Heart transplants in pediatric patients: viral infection as a loss predictor.

Towbin JA, Ware SM, Jefferies JL. Towbin JA, et al. Among authors: ware sm. Future Cardiol. 2010 Nov;6(6):735-41. doi: 10.2217/fca.10.105. Future Cardiol. 2010. PMID: 21142627 Free article. Review. No abstract available.

9

Implications for genotype-phenotype predictions in Townes-Brocks syndrome: case report of a novel SALL1 deletion and review of the literature.

Miller EM, Hopkin R, Bao L, Ware SM. Miller EM, et al. Among authors: ware sm. Am J Med Genet A. 2012 Mar;158A(3):533-40. doi: 10.1002/ajmg.a.34426. Epub 2012 Feb 3. Am J Med Genet A. 2012. PMID: 22308078 Review.

10

Pediatric cardiomyopathy: importance of genetic and metabolic evaluation.

Kindel SJ, Miller EM, Gupta R, Cripe LH, Hinton RB, Spicer RL, Towbin JA, Ware SM. Kindel SJ, et al. Among authors: ware sm. J Card Fail. 2012 May;18(5):396-403. doi: 10.1016/j.cardfail.2012.01.017. Epub 2012 Mar 10. J Card Fail. 2012. PMID: 22555271 Free PMC article.

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