Hasil Pencarian - Reshma Biniwale

  • Menampilkan 1 - 5 hasil dari 5
Perbaiki Hasil
  1. 1
    Considerations of valvular heart disease in children with ventricular assist devices

    Considerations of valvular heart disease in children with ventricular assist devices oleh Ming-Sing Si, Vikram Sood, Reshma Biniwale, David Peng, David Peng

    Diterbitkan 2023-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    Occlusion of aortopulmonary and venovenous collaterals prior to heart or combined heart-liver transplantation in Fontan patients: A single-center experience

    Occlusion of aortopulmonary and venovenous collaterals prior to heart or combined heart-liver transplantation in Fontan patients: A single-center experience oleh Weiyi Tan, Leigh Reardon, Jeannette Lin, Gentian Lluri, Prashanth Venkatesh, Katia Bravo-Jaimes, Reshma Biniwale, Glen Van Arsdell, Reid D. Ponder, Jamil Aboulhosn

    Diterbitkan 2021-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    High-Throughput Genomics Identify Novel <em>FBN1/2</em> Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects

    High-Throughput Genomics Identify Novel <em>FBN1/2</em> Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects oleh Gloria K. E. Zodanu, John H. Hwang, Zubin Mehta, Carlos Sisniega, Alexander Barsegian, Xuedong Kang, Reshma Biniwale, Ming-Sing Si, Gary M. Satou, Nancy Halnon, UCLA Congenital Heart Defect BioCore Faculty, Wayne W. Grody, Glen S. Van Arsdell, Stanley F. Nelson, Marlin Touma

    Diterbitkan 2024-05-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in <i>LMOD2</i> Gene Causing Infantile Dilated Cardiomyopathy

    Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in <i>LMOD2</i> Gene Causing Infantile Dilated Cardiomyopathy oleh Reiri Sono, Tania M. Larrinaga, Alden Huang, Frank Makhlouf, Xuedong Kang, Jonathan Su, Ryan Lau, Valerie A. Arboleda, Reshma Biniwale, Gregory A. Fishbein, Negar Khanlou, Ming-Sing Si, Gary M. Satou, Nancy Halnon, UCLA Congenital Heart Defects-BioCore Faculty, Glen S. Van Arsdell, Carol C. Gregorio, Stanly Nelson, Marlin Touma

    Diterbitkan 2023-05-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    Case Report: Whole Exome Sequencing Identifies Compound Heterozygous Variants in TSFM Gene Causing Juvenile Hypertrophic Cardiomyopathy

    Case Report: Whole Exome Sequencing Identifies Compound Heterozygous Variants in TSFM Gene Causing Juvenile Hypertrophic Cardiomyopathy oleh Jamie O. Yang, Hapet Shaybekyan, Hapet Shaybekyan, Yan Zhao, Yan Zhao, Xuedong Kang, Xuedong Kang, Gregory A. Fishbein, Negar Khanlou, Juan C. Alejos, Nancy Halnon, Gary Satou, Reshma Biniwale, Hane Lee, Hane Lee, Glen Van Arsdell, Stanley F. Nelson, Stanley F. Nelson, Stanley F. Nelson, Stanley F. Nelson, Marlin Touma, Marlin Touma, Marlin Touma, Marlin Touma, Marlin Touma, Marlin Touma, Marlin Touma, the UCLA Clinical Genomics Center, the UCLA Congenital Heart Defects-BioCore Faculty

    Diterbitkan 2022-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: