Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: Syndrome and CAV3[original query] |
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Prevalence of long-QT syndrome gene variants in sudden infant death syndrome. Circulation 2007 Jan 115 (3): 361-7. Arnestad Marianne, Crotti Lia, Rognum Torleiv O, Insolia Roberto, Pedrazzini Matteo, Ferrandi Chiara, Vege Ashild, Wang Dao W, Rhodes Troy E, George Alfred L, Schwartz Peter |
Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease. Gastroenterology 2010 Jul 139 (1): 130-9.e24. Roberts Kari E, Kawut Steven M, Krowka Michael J, Brown Robert S, Trotter James F, Shah Vijay, Peter Inga, Tighiouart Hocine, Mitra Nandita, Handorf Elizabeth, Knowles James A, Zacks Steven, Fallon Michael B, |
Screening for copy number variation in genes associated with the long QT syndrome: clinical relevance. Journal of the American College of Cardiology 2010 12 57 (1): 40-7. Barc Julien, Briec François, Schmitt Sébastien, Kyndt Florence, Le Cunff Martine, Baron Estelle, Vieyres Claude, Sacher Frédéric, Redon Richard, Le Caignec Cédric, Le Marec Hervé, Probst Vincent, Schott Jean-Jacqu |
Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics. The Canadian journal of cardiology 0 28 (2): 196-200. Holst Anders G, Saber Siamak, Houshmand Massoud, Zaklyazminskaya Elena V, Wang Yinman, Jensen Henrik Kjærulf, Refsgaard Lena, Haunsø Stig, Svendsen Jesper Hastrup, Olesen Morten S, Tfelt-Hansen Jac |
Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory. Genetic testing and molecular biomarkers 2013 Jul 17 (7): 553-61. Lieve Krystien V, Williams Leah, Daly Amy, Richard Gabriele, Bale Sherri, Macaya Daniela, Chung Wendy |
Mutations in genes encoding cardiac ion channels previously associated with sudden infant death syndrome (SIDS) are present with high frequency in new exome data. The Canadian journal of cardiology 2013 Sep 29 (9): 1104-9. Andreasen Charlotte, Refsgaard Lena, Nielsen Jonas B, Sajadieh Ahmad, Winkel Bo G, Tfelt-Hansen Jacob, Haunsø Stig, Holst Anders G, Svendsen Jesper H, Olesen Morten |
Genome-wide SNP analysis of the Systemic Capillary Leak Syndrome (Clarkson disease). Rare diseases (Austin, Tex.) 2013 Dec 1 (1): 1. Xie Zhihui, Nagarajan Vijayaraj, Sturdevant Daniel E, Iwaki Shoko, Chan Eunice, Wisch Laura, Young Michael, Nelson Celeste M, Porcella Stephen F, Druey Kirk |
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome. PloS one 2015 10 (7): e0133037. Allegue Catarina, Coll Mònica, Mates Jesus, Campuzano Oscar, Iglesias Anna, Sobrino Beatriz, Brion Maria, Amigo Jorge, Carracedo Angel, Brugada Pedro, Brugada Josep, Brugada Ram |
Retrospective Genetic Analysis of 200 Cases of Sudden Infant Death Syndrome and Its Relationship with Long QT Syndrome in Korea. Journal of Korean medical science 2018 8 33 (32): e200. Son Min-Jeong, Kim Min-Kyoung, Yang Kyung-Moo, Choi Byung-Ha, Lee Bong Woo, Yoo Seong |
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- Page last updated:May 06, 2024
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