Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Fibrosis and SCD[original query] |
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| Mannose-binding lectin 2 gene polymorphism and lung damage in primary ciliary dyskinesia. Pediatric pulmonology 2015 Feb 50 (2): 179-86. Pifferi Massimo, Bush Andrew, Michelucci Angela, Di Cicco Maria, Piras Martina, Caramella Davide, Mazzei Federica, Neri Maria, Pioggia Giovanni, Tartarisco Gennaro, Saggese Giuseppe, Simi Paolo, Boner Attilio |
| Risk stratification in pediatric hypertrophic cardiomyopathy: Insights for bridging the evidence gap? Progress in pediatric cardiology 2019 5 49 31-37. Nakano Stephanie J, Menon Shaji |
| Genetic contributions to the expression of acquired causes of cardiac hypertrophy in non-ischemic sudden cardiac death victims. Scientific reports 2021 5 11 (1): 11171. Holmström Lauri, Pylkäs Katri, Tervasmäki Anna, Vähätalo Juha, Porvari Katja, Pakanen Lasse, Kaikkonen Kari S, Perkiömäki Juha S, Kiviniemi Antti M, Kerkelä Risto, Ukkola Olavi, Myerburg Robert J, Huikuri Heikki V, Junttila Juha |
| Priapism in sickle cell disease: Associations between NOS3 and EDN1 genetic polymorphisms and laboratory biomarkers. PloS one 2021 16 (2): e0246067. Figueiredo Camylla Vilas Boas, Santiago Rayra Pereira, da Guarda Caroline Conceição, Oliveira Rodrigo Mota, Fiuza Luciana Magalhães, Yahouédéhou Sètondji Cocou Modeste Alexandre, Carvalho Suéllen Pinheiro, Neres Joelma Santana Dos Santos, Oliveira Antonio Mateus de Jesus, Fonseca Cleverson Alves, Nascimento Valma Maria Lopes, Lyra Isa Menezes, Aleluia Milena Magalhães, Goncalves Marilda Sou |
| Compound Mutation in Cardiac Sarcomere Proteins Is Associated with Increased Risk for Major Arrhythmic Events in Pediatric Onset Hypertrophic Cardiomyopathy. Journal of clinical medicine 2021 Nov 10 (22): . Pollmann Kathrin, Kaltenecker Emanuel, Schleihauf Julia, Ewert Peter, Görlach Agnes, Wolf Cordula |
| Filamin-C variant-associated cardiomyopathy: A pooled analysis of individual patient data to evaluate the clinical profile and risk of sudden cardiac death. Heart rhythm 2021 Sep . Celeghin Rudy, Cipriani Alberto, Bariani Riccardo, Bueno Marinas Maria, Cason Marco, Bevilacqua Michela, De Gaspari Monica, Rizzo Stefania, Rigato Ilaria, Da Pozzo Stefano, Zorzi Alessandro, Perazzolo Marra Martina, Thiene Gaetano, Iliceto Sabino, Basso Cristina, Corrado Domenico, Pilichou Kalliopi, Bauce Barba |
| Genetic Variants Associated With Sudden Cardiac Death in Victims With Single Vessel Coronary Artery Disease and Left Ventricular Hypertrophy With or Without Fibrosis. Frontiers in cardiovascular medicine 2021 8 755062. Vähätalo Juha H, Holmström Lauri T A, Pylkäs Katri, Skarp Sini, Porvari Katja, Pakanen Lasse, Kaikkonen Kari S, Perkiömäki Juha S, Kerkelä Risto, Huikuri Heikki V, Myerburg Robert J, Junttila M Juha |
| Novel Genetic Variants Associated with Primary Myocardial Fibrosis in Sudden Cardiac Death Victims. Journal of cardiovascular translational research 2024 6 . Sini Skarp, Anne Doedens, Lauri Holmström, Valerio Izzi, Samu Saarimäki, Eeva Sliz, Johannes Kettunen, Lasse Pakanen, Risto Kerkelä, Katri Pylkäs, Heikki V Huikuri, Robert J Myerburg, Juhani Juntti |
| Genetic variants associated with cardiac hypertrophy-related sudden cardiac death and cardiovascular outcomes in a Finnish population. Heart (British Cardiac Society) 2024 10 . Anne Doedens, Sini Skarp, Lauri Holmström, Lasse Pakanen, Samu Saarimäki, Risto Kerkelä, Katri Pylkäs, Heikki V Huikuri, Juhani Juntti |
| Characterization of cardiac involvement in patients with LMNA splice-site mutation-related dilated cardiomyopathy and sudden cardiac death. Frontiers in genetics 2024 1 14 1291411. Xuebin Ling, Yanjun Hou, Xingyu Jia, Youling Lan, Xiaoping Wu, Julan Wu, Wei Jie, Hui Liu, Shan Huang, Zhenling Wan, Tianfa Li, Junli Guo, Tiebiao Lia |
- Page last reviewed:Feb 1, 2024
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