Results 61 to 70 of about 107,014 (181)
Background Aortic stenosis (AS) in combination with left ventricular outflow tract obstruction (LVOTO) has occasionally been reported. However, making a precise diagnosis and successfully treating this combination is challenging due to the hemodynamic ...
Qingwen Kang +5 more
semanticscholar +1 more source
Etude de l'évolution des patients porteurs d'une cardiomyopathie hypertrophique obstructive (CMHO) après alcoolisation septale [PDF]
La cardiomyopathie hypertrophique (CMH) est la maladie cardiaque monogénique la plus fréquente, touchant environ 1 individu sur 500 dans la population (1,2).
CARREL, L.
core
ABSTRACT Background Hypertrophic obstructive cardiomyopathy (HOCM) is a hereditary myocardial disease. Percutaneous endocardial septal radiofrequency ablation (PESA) is an innovative approach for treating HOCM. Consequently, we present the outcomes of the PESA for HOCM. Methods This study included 20 patients with HOCM who received PESA.
NingNing Zheng +6 more
wiley +1 more source
Echocardiographic findings late after myectomy in hypertrophic obstructive cardiomyopathy [PDF]
Postoperative echocardiograms of 50 patients undergoing myectomy for hypertrophic obstructive cardiomyopathy between 1965 and 1982 have been evaluated. In 21 patients a comparison with preoperative echocardiograms showed that postoperatively there was a ...
JENNI, R. +4 more
core
Introduction The aim of our study is to compare the early and mid-term outcomes of patients with hypertrophic obstructive cardiomyopathy who underwent classic and modified Morrow septal myectomy. Methods Between 2014 and 2019, 48 patients (24 males; mean
Mustafa Karaarslan +2 more
semanticscholar +1 more source
Symptomatic aortic valve stenosis (AS) is associated with asymmetric basal septal hypertrophy (ABSH) in 10% of cases. In this cohort, it has been suggested that rectification of the left ventricular outflow tract obstruction (LVOTO) by concomitant septal
G. Karapanagiotidis +9 more
semanticscholar +1 more source
Abstract Aims Hypertrophic cardiomyopathy (HCM) is an inherited cardiomyopathy often caused by pathogenic variants in MYBPC3 and MYH7, encoding myosin‐binding protein C3 and myosin heavy chain 7, respectively. These variants can cause increased actin–myosin crossbridge cycling, resulting in ventricular hypercontractility, but mice lacking Mybpc3 ...
Isabell Yan +10 more
wiley +1 more source
Expressão fenotípica da miocardiopatia hipertrófica e realce tardio na ressonância magnética cardíaca [PDF]
INTRODUCTION AND AIM: The prognostic value of late gadolinium enhancement (LGE) for risk stratification of hypertrophic cardiomyopathy (HCM) patients is the subject of disagreement.
Almeida, I +8 more
core +1 more source
Myectomy versus alcohol septal ablation in patients with hypertrophic obstructive cardiomyopathy [PDF]
OBJECTIVES: There is very little evidence comparing the safety and efficacy of alcohol septal ablation versus septal myectomy for a septal reduction in patients with hypertrophic obstructive cardiomyopathy.
Afanasyev, A. V. +8 more
core +2 more sources
Echocardiographic Features of Cardiomyopathies: A Comprehensive Review
Echocardiography remains a cornerstone in the diagnosis and characterization of cardiomyopathies, offering detailed structural and functional insights. This review outlines key echocardiographic features that guide the evaluation of dilated, hypertrophic, restrictive, and non‐compaction cardiomyopathies, enhancing clinical decision‐making.
Ghassan Hamdan Al‐Naami
wiley +1 more source

