תוצאות חיפוש - Teresa Kruisselbrink
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Evaluation of the Mayo Clinic Phenotype-Based Genotype Predictor Score in Patients with Clinically Diagnosed Hypertrophic Cardiomyopathy מאת Sinéad Murphy, Jason H. Anderson, Jamie D. Kapplinger, Teresa Kruisselbrink, Bernard J. Gersh, Steve R. Ommen, Michael J. Ackerman, J. Martijn Bos
יצא לאור 2016Artigo -
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Scalable system-wide CYP2C19 pharmacogenomic testing reveals 38% excess incidence of adverse events in metabolizers receiving inappropriate prescriptions מאת Natalie Telis, Douglas Stoller, Christopher N. Chapman, C. Anwar A. Chahal, Daniel P. Judge, Douglas A. Olson, Joseph J. Grzymski, Teresa Kruisselbrink, Nicole L. Washington, Elizabeth T. Cirulli
יצא לאור 2025Pré-impressão -
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Incorporating a Genetic Risk Score Into Coronary Heart Disease Risk Estimates מאת Iftikhar J. Kullo, Hayan Jouni, Erin Austin, Sherry‐Ann Brown, Teresa Kruisselbrink, Iyad Isseh, Raad A. Haddad, Tariq S. Marroush, Khader Shameer, Janet E. Olson, Ulrich Broeckel, Robert C. Green, Daniel J. Schaid, Víctor M. Montori, Kent R. Bailey
יצא לאור 2016Artigo -
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A Case for Inclusion of Genetic Counselors in Cardiac Care מאת Patricia Arscott, Colleen Caleshu, Katrina E. Kotzer, Sarah Kreykes, Teresa Kruisselbrink, Kate M. Orland, Christina Rigelsky, Emily Smith, Katherine G. Spoonamore, Joy Larsen Haidle, Monica Marvin, Michael J. Ackerman, Azam Hadi, Arya Mani, Steven R. Ommen, Sara Cherny
יצא לאור 2015Revisão -
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De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias מאת Katherine L. Helbig, Robert J. Lauerer, Jacqueline C Bahr, Ivana A. Souza, Candace T. Myers, Betül Seher Uysal, Niklas Schwarz, María A. Gandini, Sun Huang, Boris Keren, Cyril Mignot, Alexandra Afenjar, Thierry Billette de Villemeur, Delphine Héron, Caroline Nava, Stéphanie Valence, Julien Buratti, Christina Fagerberg, Kristina P. Soerensen, Maria Kibæk, Erik‐Jan Kamsteeg, David A. Koolen, Boudewijn Gunning, Helenius J. Schelhaas, Michael C. Kruer, Jordana Fox, Somayeh Bakhtiari, Randa Jarrar, Sergio Padilla-López, Kristin Lindstrom, Sheng Chih Jin, Xue Zeng, Kaya Bilgüvar, Antigone Papavasileiou, Qinghe Xing, Changlian Zhu, Katja Boysen, Filippo Pinto e Vairo, Brendan C. Lanpher, Eric W. Klee, Jan‐Mendelt Tillema, Eric T. Payne, Margot A. Cousin, Teresa Kruisselbrink, Myra J. Wick, Joshua Baker, Eric Haan, Nicholas Smith, Azita Sadeghpour, Erica E. Davis, Nicholas Katsanis, Mark Corbett, Alastair H. MacLennan, Jozef Gécz, Saskia Biskup, Eva Goldmann, Lance H. Rodan, Elizabeth Kichula, Eric Segal, Kelly E. Jackson, Alexander Asamoah, David Dimmock, Julie McCarrier, Lorenzo D. Botto, Francis Filloux, Tatiana Tvrdik, Gregory D. Cascino, Sherry Klingerman, Catherine M. Neumann, Raymond Wang, Jessie C. Jacobsen, Melinda Nolan, Russell G. Snell, Klaus Lehnert, Lynette G. Sadleir, Britt‐Marie Anderlid, Malin Kvarnung, Renzo Guerrini, Michael J. Friez, Michael J. Lyons, Jennifer Leonhard, Gabriel Kringlen, Kari Casas, Christelle Moufawad El Achkar, Lacey Smith, Alexander Rotenberg, Annapurna Poduri, Alba Sanchis‐Juan, Keren Carss, Julia Rankin, Adam Zeman, F. Lucy Raymond, Moira Blyth, Bronwyn Kerr, Karla Ruiz, Jill Urquhart, Imelda Hughes, Siddharth Banka, Ulrike B. S. Hedrich, Ingrid E. Scheffer
יצא לאור 2018Artigo
כלי חיפוש:
נושאים קשורים
Medicine
Internal medicine
Biology
Cardiology
Genetic testing
Genetics
Cohort
Disease
Gene
Hypertrophic cardiomyopathy
Adverse effect
Anatomy
Asymptomatic
Atherosclerotic cardiovascular disease
CYP2C19
Cholesterol
Confidence interval
Coronary heart disease
Cytochrome P450
Demography
Dystonia
Economic growth
Economics
Encephalopathy
Epilepsy
Family medicine
Framingham Risk Score
Gene isoform
Genetic counseling
Genotype