Zobrazeno 1 - 10
of 29
pro vyhledávání: '"521"'
Autor:
Minjae Yoon, Jin Joo Park, Taeho Hur, Cam-Hao Hua, Chi Young Shim, Byung-Su Yoo, Hyun-Jai Cho, Seonhwa Lee, Hyue Mee Kim, Ji-Hyun Kim, Sungyoung Lee, Dong-Ju Choi
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundBecause of the short half-life of non-vitamin K antagonist oral anticoagulants (NOACs), consistent drug adherence is crucial to maintain the effect of anticoagulants for stroke prevention in atrial fibrillation (AF). Considering the low adh
Externí odkaz:
https://doaj.org/article/d69df379fee94846a7b24cd1d25055ed
Autor:
Wan Cheol Kim, MD, FRCPC, Edmond Lemire, MD, PhD, FRCPC, FCCMG, Siddarth Nosib, BSc, Shravankumar Nosib, MD, FRCPC
Publikováno v:
CJC Open, Vol 3, Iss 11, Pp 1383-1387 (2021)
A novel frameshift mutation in the KCNH2 gene for long QT syndrome type 2 (LQTS2) was identified after torsades des pointes ventricular tachycardia in a 49-year-old patient managed with octreotide and nadolol for an acute variceal bleed. In spite of
Externí odkaz:
https://doaj.org/article/8277df5db7aa427289eeecfc6dac88f2
Autor:
Jiawen Li, Xiaofang Tang, Jingjing Xu, Ru Liu, Lin Jiang, Lianjun Xu, Jian Tian, Xinxing Feng, Yajie Wu, Yin Zhang, Dong Wang, Kai Sun, Bo Xu, Wei Zhao, Rutai Hui, Runlin Gao, Lei Song, Jinqing Yuan, Xueyan Zhao
Publikováno v:
BMC Cardiovascular Disorders, Vol 23, Iss 1, Pp 1-9 (2023)
Abstract Background To investigate the association of HMGCR and NPC1L1 gene polymorphisms with residual cholesterol risk (RCR) in patients with premature triple-vessel disease (PTVD). Methods Three SNPs within HMGCR including rs12916, rs2303151, and
Externí odkaz:
https://doaj.org/article/96f1defc7b9b4d99b0a88073d12be412
Autor:
Girish Pathangey, Susan P D’Anna, Rohitha A. Moudgal, David B. Min, Katharine A. Manning, Cynthia C. Taub, Lauren G. Gilstrap
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
PurposeTo evaluate the safety, efficacy, and outcomes of outpatient intravenous diuresis in a rural setting and compare it to urban outcomes.MethodsA single-center study was conducted on 60 patients (131 visits) at the Dartmouth-Hitchcock Medical Cen
Externí odkaz:
https://doaj.org/article/101a81f61986488298f4379285aa2e27
Autor:
Rania Hammami, Slim Abid, Jdidi Jihen, Zied Triki, Imtinene Ben Mrad, Amine Kammoun, Mehdi Slim, Marwen Kacem, Houssem Thabet, Aymen Ben Abdessalem, Souad Mallek, Selma Charfeddine, Faten Triki, Samia Ernez Hejri, Ilyes Naffeti, Hicheme Denguir, Sondos Kraeim, Leila Abid
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundRadial artery occlusion (RAO) remains the most frequent complication of trans-radial access. Once the radial artery is occluded, its future use as an access site for coronary procedures, or as a conduit for coronary bypass grafting or fistu
Externí odkaz:
https://doaj.org/article/a6eb284b469c4aae965cac85b531f87f
Autor:
Ernesto Curty, Fernando Eugênio dos Santos Cruz, Fabiane Santos Lima, Jorge Luiz Albuquerque Coutinho, Rosane Silva, Turán Peter Ürményi, Antônio Carlos Campos Carvalho, Edson Rondinelli
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 96, Iss 3, Pp 172-178 (2011)
FUNDAMENTO: A síndrome do QT longo (SQTL) é uma síndrome arrítmica herdada com aumento do intervalo QT e risco de morte súbita. Mutações nos genes KCNQ1, KCNH2 e SCN5A respondem por 90% dos casos com genótipo determinado, e a genotipagem é i
Externí odkaz:
https://doaj.org/article/1cf5998e8d284b7797be5a0402cb72c3
Publikováno v:
Indian Pacing and Electrophysiology Journal, Vol 22, Iss 1, Pp 18-23 (2022)
Background: This review aims to determine if patients who undergo atrial fibrillation (AF) ablation with heart failure with preserved ejection fraction (HFpEF) do better, or worse or the same compared to patients with heart failure with reduced eject
Externí odkaz:
https://doaj.org/article/78ddc6f5cefb4a548aefec4eb54d87b7
Autor:
Rui-Bing Niu, Xiao-Xian Dong, Li-Ping Guo, Li Pan, Yue-Qin Hai, Xiao-Xiao Chen, Bao-Sheng Duan
Publikováno v:
Clinical and Experimental Hypertension, Vol 43, Iss 8, Pp 788-792 (2021)
Objective This study aimed to analyze the influence of SLCO1B1 and APOE gene polymorphisms on coronary heart disease in Mongolian population who living in Ordos area. Methods From January 2019 to June 2020, 200 Mongolian patients with coronary heart
Externí odkaz:
https://doaj.org/article/67d32d12d4e941c48030ae491c1b4453
Autor:
Aliza Hussain, Salim S. Virani, Luke Zheng, Ty J. Gluckman, William B. Borden, Frederick A. Masoudi, Thomas M. Maddox
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 11, Iss 11 (2022)
Background Clinical implications of change in the 2017 American College of Cardiology (ACC)/American Heart Association (AHA) guideline on the diagnosis and management of hypertension, compared with recommendations by 2014 expert panel and Seventh Rep
Externí odkaz:
https://doaj.org/article/8ce65d14ec084e56b698e3b6db86558d
Autor:
Tadashi Nakajima, Tommy Dharmawan, Reika Kawabata‐Iwakawa, Shuntaro Tamura, Hiroshi Hasegawa, Takashi Kobari, Masaki Ota, Shoichi Tange, Masahiko Nishiyama, Yoshiaki Kaneko, Masahiko Kurabayashi
Publikováno v:
Annals of Noninvasive Electrocardiology, Vol 26, Iss 3, Pp n/a-n/a (2021)
Abstract Background SCN5A‐related Brugada syndrome (BrS) can be caused by multiple mechanisms including trafficking defects and altered channel gating properties. Most SCN5A mutations at pore region cause trafficking defects, and some of them can b
Externí odkaz:
https://doaj.org/article/7f581cf3e4594759af2b0237dd9422a7