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Pediatric Cardiomyopathies.
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: miller em. Circ Res. 2017 Sep 15;121(7):855-873. doi: 10.1161/CIRCRESAHA.116.309386. Circ Res. 2017. PMID: 28912187 Free PMC article. Review.
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: miller em. 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.
Genetic testing practices in infants with congenital heart disease.
Connor JA, Hinton RB, Miller EM, Sund KL, Ruschman JG, Ware SM. Connor JA, et al. Among authors: miller em. Congenit Heart Dis. 2014 Mar-Apr;9(2):158-67. doi: 10.1111/chd.12112. Epub 2013 Jun 20. Congenit Heart Dis. 2014. PMID: 23782710
Novel Timothy syndrome mutation leading to increase in CACNA1C window current.
Boczek NJ, Miller EM, Ye D, Nesterenko VV, Tester DJ, Antzelevitch C, Czosek RJ, Ackerman MJ, Ware SM. Boczek NJ, et al. Among authors: miller em. Heart Rhythm. 2015 Jan;12(1):211-9. doi: 10.1016/j.hrthm.2014.09.051. Epub 2014 Sep 28. Heart Rhythm. 2015. PMID: 25260352 Free PMC article.
Aortopathy in the 7q11.23 microduplication syndrome.
Parrott A, James J, Goldenberg P, Hinton RB, Miller E, Shikany A, Aylsworth AS, Kaiser-Rogers K, Ferns SJ, Lalani SR, Ware SM. Parrott A, et al. Am J Med Genet A. 2015 Feb;167A(2):363-70. doi: 10.1002/ajmg.a.36859. Epub 2014 Nov 26. Am J Med Genet A. 2015. PMID: 25428557 Free article.
323 results