Showing 121 - 140 results of 472 for search '"Cardiomyopathy"', query time: 0.05s Refine Results
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    Malouf Syndrome with Hypergonadotropic Hypogonadism and Cardiomyopathy: Two-Case Report and Literature Review by Dilek Benk Şilfeler, Atilla Karateke, Raziye Keskin Kurt, Özgür Aldemir, Alper Buğra Nacar, Ali Baloğlu

    Published 2014-01-01
    “…Malouf syndrome is a very rarely encountered syndrome which was first diagnosed in 1985 upon the examination of two sisters, with findings of hypergonadotropic hypogonadism, dilated cardiomyopathy, blepharoptosis, and broad nasal base. …”
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    Article
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    The Current Approach to Diagnosis and Management of Left Ventricular Noncompaction Cardiomyopathy: Review of the Literature by Courtney E. Bennett, Ronald Freudenberger

    Published 2016-01-01
    “…Isolated left ventricular noncompaction (LVNC) is a genetic cardiomyopathy characterized by prominent ventricular trabeculations and deep intertrabecular recesses, or sinusoids, in communication with the left ventricular cavity. …”
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    Severe Hyponatremia-Induced Stress Cardiomyopathy: A Case Report and Review of Literature by Irushna Perera, Sanjeewa Rajapakse, Shamila T. De Silva

    Published 2020-01-01
    “…Takotsubo or stress cardiomyopathy is a non ischemic disease affecting the myocardium, which presents with typical features of myocardial ischemia. …”
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  7. 127

    Diagnosis of Turner syndrome after presenting with ischemic cardiomyopathy: A case report by Hui Zheng, Liting Guo, Yanwei Wei, Yunqiang Zhang, Yanfang Guan

    Published 2025-02-01
    “…Untreated Turner syndrome increases the risk of ischemic cardiomyopathy. We report a 44-year-old Chinese woman who was diagnosed with Turner syndrome owing to symptoms of ischemic cardiomyopathy and heart failure confirmed through cardiac magnetic resonance imaging, coronary angiography, and abnormal brain natriuretic peptide levels. …”
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  8. 128

    Metallothioneins 1 and 2 Modulate Inflammation and Support Remodeling in Ischemic Cardiomyopathy in Mice by Georg D. Duerr, Daniela Dewald, Eva J. Schmitz, Luise Verfuerth, Katharina Keppel, Christine Peigney, Alexander Ghanem, Armin Welz, Oliver Dewald

    Published 2016-01-01
    “…Repetitive brief ischemia and reperfusion (I/R) is associated with left ventricular dysfunction during development of ischemic cardiomyopathy. We investigated the role of zinc-donor proteins metallothionein MT1 and MT2 in a closed-chest murine model of I/R. …”
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    Refractory cardiogenic shock in hypertrophic cardiomyopathy complicated by apical ballooning: A case report by Matej Strycek, Rostislav Polasek, Pavol Tomasov, Jiri Karasek

    Published 2025-02-01
    “…Hypertrophic cardiomyopathy can be accompanied by dynamic obstruction in the left ventricular outflow tract and acute apical ballooning, which are among the very rare causes of cardiogenic shock. …”
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    Cardiac Transplantation following Cobalt Cardiomyopathy from Bilateral Metal-on-Metal Hip Replacements by Peter Szedlak, Amrik Virdi, Paul Cacciottolo, Stephen Shepherd, Stephen Pettit, Florian Falter

    Published 2022-01-01
    “…Following a prolonged period of deterioration without a clear cause, the diagnosis of cobalt toxicity-related cardiomyopathy due to cobalt-chromium alloy hip prostheses was eventually made. …”
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    Hypertrophic Cardiomyopathy Mimicking Acute Anterior Myocardial Infarction Associated with Sudden Cardiac Death by Y. Daralammouri, M. El Garhy, K. Same, B. Lauer

    Published 2012-01-01
    “…Hypertrophic cardiomyopathy is the most common genetic disease of the heart. …”
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    Can Serum Tenascin-C Be Used as a Marker of Inflammation in Patients with Dilated Cardiomyopathy? by Alyaa A. Kotby, Manal M. Abdel Aziz, Waleed M. El Guindy, Amira N. Moneer

    Published 2013-01-01
    “…To evaluate the role of TN-C as a marker for active inflammation in children with dilated cardiomyopathy (DCM). Subjects and Methods. 24 consecutive patients with primary nonfamilial DCM aged 6–72 months (mean 45.19±11.03) were divided into group I, twelve patients with acute onset DCM (<6 months duration), and group II, twelve patients with chronic DCM (>6 months duration), and compared to 20 healthy age- and sex-matched controls. …”
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