Zobrazeno 1 - 10
of 151
pro vyhledávání: '"cardiac conduction disease"'
Autor:
Giuseppe Di Stolfo, Sandra Mastroianno, Nicolò Soldato, Raimondo Salvatore Massaro, Giovanni De Luca, Davide Seripa, Maria Urbano, Carolina Gravina, Antonio Greco, Paola Siena, Marco Matteo Ciccone, Andrea Igoren Guaricci, Cinzia Forleo, Massimo Carella, Domenico Rosario Potenza
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 11, p 3177 (2024)
Aims: TOMM40 single nucleotide polymorphism (SNP) rs2075650 consists of allelic variation c.275-31A > G and it has been linked to Alzheimer disease, apolipoprotein and cholesterol levels and other risk factors. However, data on its role in cardiovasc
Externí odkaz:
https://doaj.org/article/bb1b4972a21d4f76aa36dfe57b77923d
Autor:
Maoxiang Zhao, Jingli Gao, Shuohua Chen, Siyu Yao, Miao Wang, Chi Wang, Sijin Zhang, Zekun Feng, Lu Tian, Yanjie Li, Yang Liu, Shouling Wu, Hao Xue
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 24 (2023)
Background Cardiac conduction diseases can lead to life‐threatening outcomes. However, the evidence on risk factors for conduction disease that is needed to underpin prevention strategies is limited. The present study aimed to determine the associa
Externí odkaz:
https://doaj.org/article/60096fa4153c433e8adf5e12326e23d5
Autor:
Lv Xuejiao, Sun Yuxin, Tan Wenxi, Liu Yang, Wen Naiyan, Fu Shuang, Yu Lanying, Liu Tiantian, Qi Xiaocui, Shu Nanqi, Du Yanwei, Zhang Wenfeng, Meng Yan
Publikováno v:
Open Life Sciences, Vol 16, Iss 1, Pp 1240-1251 (2021)
Externí odkaz:
https://doaj.org/article/bea64f78578f488fb43cb938916e82f6
Akademický článek
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Autor:
Laia Brunet Garcia, Ankita Hajra, Ella Field, Joseph Wacher, Helen Walsh, Gabrielle Norrish, Adnan Manzur, Francesco Muntoni, Pinki Munot, Stephanie Robb, Rosaline Quinlivan, Mariacristina Scoto, Giovanni Baranello, Anna Sarkozy, Luke Starling, Juan Pablo Kaski, Elena Cervi
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Myotonic dystrophy type 1 (DM1) is the most prevalent inherited neuromuscular dystrophy in adults. It is a multisystem disease with cardiac manifestations. Whilst these are well-defined in adults, there are scarce published data in the pediatric popu
Externí odkaz:
https://doaj.org/article/3fb4b718270d4f3b9aae0d632cd63a13
Publikováno v:
Physiological Reports, Vol 9, Iss 22, Pp n/a-n/a (2021)
Abstract Variants in the LMNA gene, which encodes for Lamin A/C, are associated with cardiac conduction disease (CCD). We previously reported that Lamin A/C variants p.R545H and p.A287Lfs*193, which were identified in CCD patients, decreased peak INa
Externí odkaz:
https://doaj.org/article/7aaf40cbff3446268244b82cff02bd1c
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Malfunction in the cardiac conduction system (CCS) due to congenital anomalies or diseases can cause cardiac conduction disease (CCD), which results in disturbances in cardiac rhythm, leading to syncope and even sudden cardiac death. Insights into de
Externí odkaz:
https://doaj.org/article/dbb4ee7be0a54b058efe65cabedebebb
Autor:
Aaron Isaacs, Andrei Barysenka, Rachel M.A. ter Bekke, Apollonia T.J.M. Helderman-van den Enden, Arthur van den Wijngaard, Paul G.A. Volders, Monika Stoll
Publikováno v:
Heart Rhythm. 20(5):720-727
Background: The Worm Study, ascertained from a multigeneration pedigree segregating a single amino acid deletion in SCN5A (c.4850_4852delTCT, p.(Phe1617del), rs749697698), is characterized by substantial phenotypic heterogeneity and overlap of sudden
Autor:
Alberto Palladino, Andrea Antonio Papa, Roberta Petillo, Marianna Scutifero, Salvatore Morra, Luigia Passamano, Vincenzo Nigro, Luisa Politano
Publikováno v:
Genes, Vol 13, Iss 2, p 258 (2022)
Progressive cardiac conduction disease (PCCD) is a relatively common condition in young and elderly populations, related to rare mutations in several genes, including SCN5A, SCN1B, LMNA and GJA5, TRPM4. Familial cases have also been reported. We desc
Externí odkaz:
https://doaj.org/article/0921b28293c24695865becd4c8d43db6