Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Arrhythmia and LMNA[original query] |
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| Variants of the lamin A/C (LMNA) gene in non-valvular atrial fibrillation patients: a possible pathogenic role of the Thr528Met mutation. Molecular diagnosis & therapy 2012 Apr 16 (2): 99-107. Saj Michal, Dabrowski Rafal, Labib Sarah, Jankowska Agnieszka, Szperl Malgorzata, Broda Grazyna, Szwed Hanna, Tesson Frederique, Bilinska Zofia T, Ploski Raf |
| Lamin mutation location predicts cardiac phenotype severity: combined analysis of the published literature. Open heart 2018 11 5 (2): e000915. Captur Gabriella, Arbustini Eloisa, Syrris Petros, Radenkovic Dina, O'Brien Ben, Mckenna William J, Moon James |
| Can Circulating Cardiac Biomarkers Be Helpful in the Assessment of LMNA Mutation Carriers? Journal of clinical medicine 2020 May 9 (5): . Chmielewski Przemyslaw, Michalak Ewa, Kowalik Ilona, Franaszczyk Maria, Sobieszczanska-Malek Malgorzata, Truszkowska Grazyna, Stepien-Wojno Malgorzata, Biernacka Elzbieta Katarzyna, Foss-Nieradko Bogna, Lewandowski Michal, Oreziak Artur, Bilinska Maria, Kusmierczyk Mariusz, Tesson Frédérique, Grzybowski Jacek, Zielinski Tomasz, Ploski Rafal, Bilinska Zofia |
| Predicting sustained ventricular arrhythmias in dilated cardiomyopathy: a meta-analysis and systematic review. ESC heart failure 2020 4 7 (4): 1430-1441. Sammani Arjan, Kayvanpour Elham, Bosman Laurens P, Sedaghat-Hamedani Farbod, Proctor Tanja, Gi Weng-Tein, Broezel Alicia, Jensen Katrin, Katus Hugo A, Te Riele Anneline S J M, Meder Benjamin, Asselbergs Folkert |
| Cardiac phenotype in familial partial lipodystrophy. Clinical endocrinology 2021 1 94 (6): 1043-1053. Eldin Abdelwahab Jalal, Akinci Baris, da Rocha Andre Monteiro, Meral Rasimcan, Simsir Ilgin Yildirim, Adiyaman Suleyman Cem, Ozpelit Ebru, Bhave Nicole, Gen Ramazan, Yurekli Banu, Ozdemir Kutbay Nilufer, Siklar Zeynep, Neidert Adam H, Hench Rita, Tayeh Marwan K, Innis Jeffrey W, Jalife Jose, Oral Hakan, Oral Elif |
| Prevalence and Phenotypic Burden of Monogenic Arrhythmias Using Integration of Electronic Health Records With Genetics. Circulation. Genomic and precision medicine 2022 9 15 (5): e003675. Nafissi Navid A, Abdulrahim Jawan W, Kwee Lydia Coulter, Coniglio Amanda C, Kraus William E, Piccini Jonathan P, Daubert James P, Sun Albert Y, Shah Svati |
| LMNA Variants and Risk of Adult-Onset Cardiac Disease. Journal of the American College of Cardiology 2022 Jul 80 (1): 50-59. Lazarte Julieta, Jurgens Sean J, Choi Seung Hoan, Khurshid Shaan, Morrill Valerie N, Weng Lu-Chen, Nauffal Victor, Pirruccello James P, Halford Jennifer L, Hegele Robert A, Ellinor Patrick T, Lunetta Kathryn L, Lubitz Steven |
| Disease progression rate is a strong predictor of ventricular arrhythmias in patients with cardiac laminopathies: a primary prevention cohort study. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2022 11 25 (2): 634-642. Rootwelt-Norberg Christine, Skjølsvik Eystein T, Chivulescu Monica, Bogsrud Martin P, Ribe Margareth P, Aabel Eivind W, Beitnes Jan Otto, Brekke Pål H, Håland Trine F, Hasselberg Nina E, Lie Øyvind H, Haugaa Kristina |
| Ablation for Atrial Fibrillation in Patients With Rare Pathogenic Variants in Cardiomyopathy and Arrhythmia Genes. JACC. Clinical electrophysiology 2024 9 . Majd A El-Harasis, Zachary T Yoneda, Katherine C Anderson, Fei Ye, Joseph A Quintana, J Roberto Martinez-Parachini, Gregory G Jackson, Bibin T Varghese, Diane M Crawford, Lili Sun, Hollie L Williams, Matthew J O'Neill, Giovanni E Davogustto, James L Laws, Brittany S Murphy, Kelsey Tomasek, Yan Ru Su, Emily McQuillen, Emma Metz, Carly Smith, Doug Stubbs, Dakota D Grauherr, Quinn S Wells, Gregory F Michaud, Pablo Saavedra, Juan Carlos Estrada, Travis D Richardson, Sharon T Shen, Arvindh N Kanagasundram, Jay A Montgomery, Harikrishna Tandri, Christopher R Ellis, George H Crossley, Prince J Kannankeril, Lynne W Stevenson, William G Stevenson, Steven A Lubitz, Patrick T Ellinor, Dan M Roden, M Benjamin Shoemak |
| Missense and Non-Missense Lamin A/C Gene Mutations Are Similarly Associated with Major Arrhythmic Cardiac Events: A 20-Year Single-Centre Experience. Biomedicines 2024 6 12 (6): . Cinzia Forleo, Maria Cristina Carella, Paolo Basile, Eugenio Carulli, Michele Luca Dadamo, Francesca Amati, Francesco Loizzi, Sandro Sorrentino, Ilaria Dentamaro, Marco Maria Dicorato, Stefano Ricci, Rosanna Bagnulo, Matteo Iacoviello, Vincenzo Ezio Santobuono, Carlo Caiati, Martino Pepe, Jean-Francois Desaphy, Marco Matteo Ciccone, Nicoletta Resta, Andrea Igoren Guaric |
| Troponin T Assessment Allows for Identification of Mutation Carriers among Young Relatives of Patients with LMNA-Related Dilated Cardiomyopathy. Journal of clinical medicine 2024 6 13 (11): . Przemys?aw Chmielewski, Ilona Kowalik, Gra?yna Truszkowska, Ewa Michalak, Joanna Poni?ska, Agnieszka Sadowska, Katarzyna Kalin, Krzysztof Jaworski, Ilona Minota, Jolanta Krzyszto?-Russjan, Tomasz Zieli?ski, Rafa? P?oski, Zofia Teresa Bili?s |
- Page last reviewed:Feb 1, 2024
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