Results 31 to 40 of about 306,427 (235)

Successful Percutaneous Septal Alcohol Ablation After Surgical Myectomy

Biomolecules & Biomedicine, 2010
Hypertrophic obstructive cardiomyopathy (HOCM) is a primary, usually familial and genetically fixed myocardial hypertrophy, with dynamic left ventricular outflow tract obstruction.
Mehmed Kulić, Muhamed Spužić, Elnur Tahirović, Šejla Šehović, Vedad Mujačić, Darko Zorman, Vladimir Velebit   +6 more
doaj   +1 more source

Left Bundle Pacing for Left Bundle Branch Block and Intermittent Third-Degree Atrioventricular Block in a MYH7 Mutation-Related Hypertrophic Cardiomyopathy With Restrictive Phenotype in a Child

Frontiers in Pediatrics, 2020
Hypertrophic cardiomyopathy (HCM) is a group of myocardial diseases defined by cardiac hypertrophy which cannot be explained by secondary causes with a non-dilated left ventricle and preserved or increased ejection fraction.
Luyan Zhang, Xueying Cheng, Jinlong Chen, Ming Zhou, Tianwei Qian, Zhongman Zhang, Jie Yin, Han Zhang, Genyin Dai, Yuming Qin, Shiwei Yang   +10 more
doaj   +1 more source

The results of alcoholic septal ablation in the treatment of hypertrophic cardiomyopathy [PDF]

Кардіохірургія та інтервенційна кардіологія, 2020
Hypertrophic obstructive cardiomyopathy іs a relatively common condition and one of the most common causes of sudden cardiac death in young age. One of the options for the surgical treatment of this pathology is septal myoectomy, which has been the gold ...
B.M. Todurov, G.I. Kovtun, A.V. Khokhlov, O.V. Pantazi, A.O. Shpachuk, A.Yu. Melnik, A.O. Maksakov, A.S. Batsiun   +7 more
doaj   +1 more source

Mid-ventricular obstructive hypertrophic cardiomyopathy [PDF]

, 2010
Mid-ventricular obstructive hypertrophic cardiomyopathy was diagnosed in a 72-year-old woman, referred to our hospital because of an episode of syncope.
Letsas, Konstantinos, Charalampous, Charalampos, Prappa, Efstathia   +2 more
core   +1 more source

Midventricular Obstructive Hypertrophic Cardiomyopathy with Apical Aneurysm: Left Ventricular Hemodynamic and Angiographic Findings: Midventricular Obstructive Hypertrophic Cardiomyopathy

, 2022
A case of a 50-year-old patient with a midventricular obstructive hypertrophic cardiomyopathy is presented and the left ventricular hemodynamic and angiographic findings are depicted and discussed.
Manolis, Antonis A., Manolis, Antonis S
core   +1 more source

Hypertrophic obstructive cardiomyopathy in a heart transplant recipient: a case report [PDF]

, 2021
The article presents a case report of developing the classic hypertrophic obstructive cardiomyopathy in a 66-year-old male heart transplant recipient within 5 years after orthotopic heart transplantation.
G. A. Golovina, N. V. Kizhvatova, E. D. Kosmacheva, T. V. Stavenchuk   +3 more
core   +1 more source

Doubly Obstructive Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2013
![Figure][1] [![Graphic][3] ][3][![Graphic][4] ][4] A 40-year-old woman with hypertrophic cardiomyopathy presented with New York Heart Association functional class III dyspnea and angina despite optimal medical therapy. Left heart catheterization with a high-fidelity,
Geske, Jeffrey B., Scantlebury, Dawn C., Nishimura, Rick A.   +2 more
openaire   +2 more sources

Heyde syndrome secondary to hypertrophic obstructive cardiomyopathy: a case report

The Egyptian Heart Journal
Background Heyde syndrome is an uncommon clinical condition characterized by the triad of aortic stenosis, gastrointestinal angiodysplasia, and acquired von Willebrand syndrome.
Abraham Castellanos-Maldonado, Gustavo Abraham Canales-Azcona, José Luis Martínez-Arroyo, Miguel Maldonado-Valdéz, Héctor Raúl Ibarra-Sifuentes   +4 more
doaj   +1 more source

Evidence of evolution towards left midventricular obstruction in severe Anderson–Fabry cardiomyopathy

ESC Heart Failure, 2021
Aims In Fabry cardiomyopathy, left ventricular outflow tract obstruction mimicking hypertrophic cardiomyopathy is a very rare finding, with few cases reported and successfully treated with cardiac surgery. In our population of patients with Fabry disease
Francesca Graziani, Rosa Lillo, Elena Panaioli, Gionata Spagnoletti, Maurizio Pieroni, Paolo Ferrazzi, Antonia Camporeale, Elena Verrecchia, Ludovico Luca Sicignano, Raffaele Manna, Filippo Crea   +10 more
doaj   +1 more source

Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy [PDF]

, 2002
Background-Although studies have suggested that "late-onset" hypertrophic cardiomyopathy (HCM) may be caused by sarcomeric protein gene mutations, the cause of HCM in the majority of patients is unknown.
Tei, C, B. Sachdev, Takenaka, T, W. J. Mckenna, Sachdev, B, H. Teraguchi, Elliott, PM, Teraguchi, H, C. Tei, P. Lee, T. Takenaka, McKenna, WJ, Lee, P, Hypertrophic Cardiomyopathy   +13 more
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