نتایج جستجو برای: hypertrophic cardiomyopathy catheterization

تعداد نتایج: 62385  

دارﻳﻮش ﺷﻴﺮاﻧﻲ

●HCM)Hypertrophic cardiomyopathy)ﻳﻚ ﺑﻴﻤﺎری ﺑﻄﻨﻲ[در درﺟﻪ اول ﺑﻄﻦ ﭼﭗ (left ventricle)] ﻣﻴﻮﻛﺎردی اﺳﺖ ﻛﻪ ﺑﻪ ﺻﻮرت ﺿﺨﻴﻢ ﺷﺪن ﺧﻔﻴﻒ ﺗﺎ ﺷﺪﻳﺪ(concentric hypertrophy) ﻣﺎﻫﻴﭽﻪ ﻫﺎی ﭘﺎﭘﻴﻼری و دﻳﻮاره ﻫﺎی ﺑﻄﻨﻲ ﺧﻮد را ﻧﺸﺎن ﻣﻴﺪﻫﺪ. واژه اوﻟﻴﻪ در اﻳﻦ زﻣﻴﻨﻪ ﺑﻪ ﻣﻌﻨﺎی اﻳﻦ اﺳﺖ ﻛﻪ hypertrophy در ﻧﺘﻴﺠﻪ ﻳﻚ ﻣﺸﻜﻞ ذاﺗﻲ در ﻣﻴﻮﻛﺎردﻳﻮم اﺗﻔﺎق ﻣﻲ اﻓﺘﺪ و ﺑﻪ ﻃﻮر ﺛﺎﻧﻮﻳﻪ در اﺛﺮ overload ﻓﺸﺎر ﻳﺎ ﺗﺤﺮﻳﻜﺎت ﻫﻮرﻣﻮﻧﻲ ﻧﻤﻲ ﺑﺎ...

نمازی, محمدحسن, نظری, نشاط ,

A number of patients with severe obstruction due to hypertrophic cardiomyopathy have derived benefit at least over the short-term from inventional infarction of a portion of the interventricular septum by the  infusion of alcohol into a selectively catheterized septal artery , with reduction of the outflow gradient and improvement in symptoms . This paper contains success...

Journal: :Journal of the American College of Cardiology 2021

Journal: :American journal of critical care : an official publication, American Association of Critical-Care Nurses 2002
Anna Barkman Judy McCay

Hypertrophic obstructive cardiomyopathy (HOCM) is an obstructive subvariety of hypertrophic cardiomyopathy. In hypertrophic cardiomyopathy, the left ventricular wall of the heart is abnormally thick, and the left ventricular cavity is small. HOCM is characterized by an excessively thick interventricular septum, which obstructs left ventricular outflow during ventricular systole. Pericardial tam...

2012
Mehmet Bulent Vatan Huseyin Gunduz Safiye Gurel Ibrahim Kocayigit Ahmet Vural Saadet Demirtas Mehmet Akif Cakar Yasemin Gunduz

Hypertrophic cardiomyopathy (HCM) is an autosomal dominant heart disease that is the most common genetic cardiac disorder. The disease is characterized by excessive thickening of the left ventricular myocardium. The anterior portion of the interventricular ventricular septum is often involved. Asymmetric hypertrophy of apical site, left ventricular free wall, and right ventricle are less common...

Journal: :Current problems in cardiology 2004
Steve R Ommen

Hypertrophic cardiomyopathy is a fascinating disease of marked heterogeneity. Hypertrophic cardiomyopathy was originally characterized by massive myocardial hypertrophy in the absence of known etiology, a dynamic left ventricular outflow obstruction, and increased risk of sudden death. It is now well accepted that multiple mutations in genes encoding for the cardiac sarcomere are responsible fo...

Journal: :British heart journal 1994
M J Davies D M Krikler

Editorial Genetic investigation and counselling of families with hypertrophic cardiomyopathy In 1958 Teare described the gross appearances of the heart in eight young people dying suddenly of what became known as hypertrophic cardiomyopathy.' The familial nature of the disease became clear when Teare found himself carrying out a necropsy on a brother of a case in the series. By coincidence on t...

Journal: :Biochemical and biophysical research communications 2003
Susumu Minamisawa Yoji Sato Yuriko Tatsuguchi Tomofumi Fujino Shin-ichiro Imamura Yoshio Uetsuka Makoto Nakazawa Rumiko Matsuoka

Phospholamban is an endogenous inhibitor of sarcoplasmic reticulum calcium ATPase and plays a prime role in cardiac contractility and relaxation. Phospholamban may be a candidate gene responsible for cardiomyopathy. We investigated genome sequence of phospholamban in patients with cardiomyopathy. PCR-based direct sequence was performed for the promoter region and the whole coding region of phos...

Journal: :British heart journal 1985
C Symons F Fortune R A Greenbaum P Dandona

Left ventricular hypertrophy (symmetric, asymmetric, or hypertrophic cardiomyopathy) is an almost invariable accompaniment of primary hyperparathyroidism. Five of 18 patients with hypertrophic cardiomyopathy had raised serum concentrations of parathyroid hormone with normal serum calcium concentrations. Left ventricular hypertrophy did not occur in any of the six patients with hypercalcaemia al...

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