Results 71 to 80 of about 15,442 (185)

Longest survivor of pulmonary atresia with ventricular septal defect without surgical intervention

ESC Heart Failure, Volume 12, Issue 2, Page 1499-1507, April 2025.
Sang Zhou, Yu Wu, Guoran Li, Yongwen Qin, Man Qi, Zhitao Jin   +5 more
wiley   +1 more source

Deep Learning‐Based Prediction Model for Cardiac Resynchronization Therapy Responders Using Electrocardiogram Data

Journal of Cardiovascular Electrophysiology, Volume 37, Issue 1, Page 157-164, January 2026.
ABSTRACT Background Cardiac resynchronization therapy (CRT) is an established treatment for advanced heart failure, but approximately 30% of patients fail to respond. This study aimed to develop and evaluate deep learning models using preimplantation electrocardiogram (ECG) data to predict CRT response.
Hitoshi Mori, Yuya Fujisaki, Syunta Higuchi, Masataka Narita, Daisuke Kawano, Kazuhisa Matsumoto, Wataru Sasaki, Tsukasa Naganuma, Naomichi Tanaka, Kazuhiko Kuinose, Haruka Yamazaki, Hiroki Yamazaki, Wataru Yoshino, Toshiki Takeda, Yoshifumi Ikeda, Ritsushi Kato   +15 more
wiley   +1 more source

Predictive value of isolated very low QRS voltage in tilt-table test for neurally mediated syncope

SAGE Open Medicine
Objective: The cause of syncope is generally determined based on clinical manifestations. There has been little discussion about the value of electrocardiograms for diagnosing neurally mediated syncope.
Haichao Chen, Yiwei Cao, Lei Liang, Yan Gao, Jing Feng, Le Zhang, Lingxia Shi, Fengjun Chang, Gong Cheng, Haoyu Wu   +9 more
doaj   +1 more source

The caveats in the diagnosis of anomalous origin of left coronary artery from pulmonary artery (ALCAPA) [PDF]

, 2010
Anomalous origin of left coronary artery from pulmonary artery (ALCAPA) is an infrequent, well described, but important anomaly of the coronary origin. Early diagnosis and prompt surgical treatment of the disease can be life saving. However, there are
Kothari, Shyam S., Varghese, M.J.
core   +1 more source

Recognizing myofascial pelvic pain in the female patient with chronic pelvic pain. [PDF]

, 2012
Myofascial pelvic pain (MFPP) is a major component of chronic pelvic pain (CPP) and often is not properly identified by health care providers. The hallmark diagnostic indicator of MFPP is myofascial trigger points in the pelvic floor musculature that ...
Katzman, Wendy B, Pastore, Elizabeth A
core   +1 more source

Heart failure in two male patients with late‐onset Fabry mutation (IVS4 + 919G > A)

ESC Heart Failure, Volume 12, Issue 2, Page 1508-1513, April 2025.
Xufei Yang, Chunlan Deng, Xiaogang Guo, Hui Yan   +3 more
wiley   +1 more source

The Relationship Between the Index of Cardio‐Electrophysiological Balance and the Non‐Dipper Hypertensive Pattern in Patients With Newly Diagnosed Hypertension

The Journal of Clinical Hypertension, Volume 28, Issue 1, January 2026.
ABSTRACT The connection between different electrocardiography (ECG) parameters and circadian blood pressure (BP) variations in patients with hypertension (HT) has been investigated. The index of cardio‐electrophysiological balance (iCEB), determined as the quotient of the QT interval and the QRS duration, offers an assessment of the comprehensive ...
Seda Tükenmez Karakurt, Hüseyin Karakurt, Nail Güven Serbest, Serkan Yazan   +3 more
wiley   +1 more source

Nonischemic ST segment elevation in hypertrophic cardiomyopathy due to chest wall deformity from kyphoscoliosis

International Medical Case Reports Journal, 2010
Aleš Blinc1, Mirjam Gubenšek1, Mišo Šabovič1, Marko Grmek2, Pavel Berden31Department of Vascular Diseases, 2Department of Nuclear Medicine, 3Department of Radiology, University Medical Centre Ljubljana ...
Aleš Blinc, Mirjam Gubenšek, Mišo Šabovič, et al   +3 more
doaj  

Transthoracic three-dimensional echocardiography in adult patients with congenital heart disease [PDF]

, 1995
Objectives: This study sought to assess both the feasibility and potential role of transthoracic three-dimensional echocardiography for the evaluation of adult patients with congenital heart disease.
Roelandt, J.R.T.C. (Jos), Salustri, A. (Alessandro), Spitaels, S.E.C. (Silja), Vletter, W.B. (Wim), Vletter-McGhie, J.S. (Jackie)   +4 more
core   +1 more source

Syndromic Congenital Heart Disease Diagnosed in Adulthood: A Reminder of the Phenotypic Variability of Alagille Syndrome

Case Reports in Cardiology, Volume 2026, Issue 1, 2026.
Alagille syndrome is a rare multisystemic genetic condition most commonly associated with neonatal liver disease. Variable expressivity is a defining feature of Alagille syndrome, resulting in a broad spectrum of phenotypic variation among individuals who meet the diagnostic criteria. We present an atypical case of cardiac‐predominant Alagille syndrome
Matthew K. Campbell, Jessica Hallam, Samuel L. Casella, Sangeeta Shah, Kathleen Ngu   +4 more
wiley   +1 more source