Search Results - Parks, Sharie B

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  1. 1
    Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

    Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy by Parks, Sharie B., PhD, Kushner, Jessica D., MS, CGC, Nauman, Deirdre, BSN, Burgess, Donna, BSN, Ludwigsen, Susan, MA, Peterson, Amanda, BS, Li, Duanxiang, MD, Jakobs, Petra, PhD, Litt, Michael, PhD, Porter, Charles B., MD, FACC, Rahko, Peter S., MD, FACC, Hershberger, Ray E., MD, FACC

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  2. 2
    Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure

    Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure by Li, Duanxiang, Parks, Sharie B., Kushner, Jessica D., Nauman, Deirdre, Burgess, Donna, Ludwigsen, Susan, Partain, Julie, Nixon, Randal R., Allen, Charles N., Irwin, Robert P., Jakobs, Petra M., Litt, Michael, Hershberger, Ray E.

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  3. 3
    Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients With Dilated Cardiomyopathy

    Clinical and Functional Characterization of TNNT2 Mutations Identified in Patients With Dilated Cardiomyopathy by Hershberger, Ray E, Pinto, Jose Renato, Parks, Sharie B, Kushner, Jessica D, Li, Duanxiang, Ludwigsen, Susan, Cowan, Jason, Morales, Ana, Parvatiyar, Michelle S, Potter, James D

    Published in Genetics (Austin)
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  4. 4
    Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy

    Coding Sequence Mutations Identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 Patients with Familial or Idiopathic Dilated Cardiomyopathy by Hershberger, Ray E., Parks, Sharie B., Kushner, Jessica D., Li, Duanxiang, Ludwigsen, Susan, Jakobs, Petra, Nauman, Deirdre, Burgess, Donna, Partain, Julie, Litt, Michael

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  5. 5
    Clinical Characteristics of 304 Kindreds Evaluated for Familial Dilated Cardiomyopathy

    Clinical Characteristics of 304 Kindreds Evaluated for Familial Dilated Cardiomyopathy by Kushner, Jessica D., Nauman, Deirdre, Burgess, Donna, Ludwigsen, Susan, Parks, Sharie B., Pantely, George, Burkett, Emily, Hershberger, Ray E.

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  6. 6
    Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypes

    Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypes by PARKS, Sharie B, POPOVICH, Bradley W, PRESS, Richard D

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