Canlyniadau Chwilio - Gabrielle C. Geddes

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  1. 1
    Language regression, hemichorea and focal subclinical seizures in a 6-year-old girl with GLUT-1 deficiency

    Language regression, hemichorea and focal subclinical seizures in a 6-year-old girl with GLUT-1 deficiency gan Alexandra M. Wood, Gabrielle C. Geddes, Ahmad Marashly

    Cyhoeddwyd 2020-01-01
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  2. 2
    Pompe disease treatment with twice a week high dose alglucoside alfa in a patient with severe dilated cardiomyopathy

    Pompe disease treatment with twice a week high dose alglucoside alfa in a patient with severe dilated cardiomyopathy gan Jesa L. Landis, Holly Hyland, Steven J. Kindel, Ann Punnoose, Gabrielle C. Geddes

    Cyhoeddwyd 2018-09-01
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  3. 3
    Skip segment Hirschsprung disease and Waardenburg syndrome

    Skip segment Hirschsprung disease and Waardenburg syndrome gan Erica R. Gross, Gabrielle C. Geddes, Julie A. McCarrier, Jason A. Jarzembowski, Marjorie J. Arca

    Cyhoeddwyd 2015-04-01
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  4. 4
    Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease

    Learning to Crawl: Determining the Role of Genetic Abnormalities on Postoperative Outcomes in Congenital Heart Disease gan Benjamin J. Landis, Benjamin M. Helm, Jeremy L. Herrmann, Madeline C. Hoover, Matthew D. Durbin, Lindsey R. Elmore, Manyan Huang, Michael Johansen, Ming Li, Leon F. Przybylowski, Gabrielle C. Geddes, Stephanie M. Ware

    Cyhoeddwyd 2022-10-01
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  5. 5
    A multi-disciplinary, comprehensive approach to management of children with heterotaxy

    A multi-disciplinary, comprehensive approach to management of children with heterotaxy gan Thomas G. Saba, Gabrielle C. Geddes, Stephanie M. Ware, David N. Schidlow, Pedro J. del Nido, Nathan S. Rubalcava, Samir K. Gadepalli, Terri Stillwell, Anne Griffiths, Laura M. Bennett Murphy, Andrew T. Barber, Margaret W. Leigh, Necia Sabin, Adam J. Shapiro

    Cyhoeddwyd 2022-09-01
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  6. 6
    Novel KLHL26 variant associated with a familial case of Ebstein’s anomaly and left ventricular noncompaction

    Novel KLHL26 variant associated with a familial case of Ebstein’s anomaly and left ventricular noncompaction gan Sai Suma K. Samudrala, Lauren M. North, Karl D. Stamm, Michael G. Earing, Michele A. Frommelt, Richard Willes, Swarnendu Tripathi, Nikita R. Dsouza, Michael T. Zimmermann, Donna K. Mahnke, Huan Ling Liang, Michael Lund, Chien‐Wei Lin, Gabrielle C. Geddes, Michael E. Mitchell, Aoy Tomita‐Mitchell

    Cyhoeddwyd 2020-04-01
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  7. 7
    A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices

    A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices gan Matthew D. Durbin, Lindsey R. Helvaty, Ming Li, William Border, Sara Fitzgerald-Butt, Vidu Garg, Gabrielle C. Geddes, Benjamin M. Helm, Seema R. Lalani, Kim L. McBride, Alexis McEntire, Dana K. Mitchell, Chaya N. Murali, Stephanie B. Wechsler, Benjamin J. Landis, Stephanie M. Ware

    Cyhoeddwyd 2023-01-01
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  8. 8
    A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease

    A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease gan Benjamin J. Landis, Lindsey R. Helvaty, Gabrielle C. Geddes, Jiuann‐Huey Ivy Lin, Svetlana A. Yatsenko, Cecilia W. Lo, William L. Border, Stephanie Burns Wechsler, Chaya N. Murali, Mahshid S. Azamian, Seema R. Lalani, Robert B. Hinton, Vidu Garg, Kim L. McBride, Jennelle C. Hodge, Stephanie M. Ware

    Cyhoeddwyd 2023-09-01
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