نتایج جستجو برای: fatal cardiomyopathy

تعداد نتایج: 82571  

2013
Ayhan YAMAN Pamir ISIK Nese YARALI Selmin KARADEMIR Semra CETINKAYA Ali BAY Serdar OZKASAP Abdurrahman KARA Bahattin TUNC

Even the life span has prolonged for the last 40 years, increase in frequently seen complications with increasing age negatively affect the life quality of thalassemia patients. In our study, complications encountered in 67 ß-thalassemia patients who were followedup at our hospital between 1 January 2004 and 31 May 2009 were retrospectively analyzed. Fifty-six patients were followed up with dia...

Journal: :Frontiers in bioscience 2009
Thora S Steffensen Enid Gilbert Barness

Conduction disorders result in cardiac arrhythmias that may be fatal. Histiocytoid cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Isolated noncompaction of the left ventricle, Long QT syndrome (LQTS) and Brugada syndrome, are all well described. Congenital short QT syndrome is a new familial primary electrical disease of the heart, which is characterized by abnormally short QT inte...

2010
James H. Jerkins Anca Suciu Sula Mazimba Alejandro Calvo

The clinical manifestations of anti-cancer drug associated cardiac side effects are diverse and can range from acutely induced cardiac arrhythmias to severe contractile dysfunction, and potentially fatal heart failure. Anthracyclines and trastuzumab cardiac toxicity have been well described and left ventricular ejection fraction (LVEF) evaluation is commonly performed before their use. Bortezom...

Journal: :Clinical chemistry 1998
D Yücel S Aydoğdu S Cehreli G Saydam H Canatan M Seneş B Ciğdem Topkaya S Nebioğlu

In the present study, we assessed oxidative stress in patients with dilated cardiomyopathy of ischemic or idiopathic etiology. For this reason we measured whole blood reduced glutathione, erythrocyte superoxide dismutase, susceptibility of erythrocyte membranes and erythrocytes to peroxidation, and SH content of erythrocyte membranes in 12 patients (8 men and 4 women, ages 31 to 66 years) with ...

Journal: :Cirugia y cirujanos 2017
Hugo Jesús Zetina-Tun Guillermo Careaga-Reyna José Galván-Díaz Magdalena Sánchez-Uribe

BACKGROUND Myocardial noncompaction of the left ventricle is a congenital cardiomyopathy characterised by left ventricular hypertrabeculation and prominent intertrabecular recesses. The incidence ranges from 0.15% to 2.2%. Clinical manifestations include heart failure, arrhythmias, and stroke. Prognosis is fatal in most cases. Heart transplantation is a therapeutic option for this cardiomyopath...

Journal: :Neurology 1983
F Usuki M Osame

Lysosomal glycogen storage disease without acid maltase deficiency is characterized by the triad of clinical manifestations (hypertrophic cardiomyopathy), mental retardation, and mild myopathy), morphologic findings (glycogen storage, glycogenosomes, and autophagic vacuoles), and normal glycolytic enzyme activities. Though most of the patients suffering from the triad were males, family studies...

2014
Lore Becker Eva Kling Evelyn Schiller Ramona Zeh Anja Schrewe Sabine M. Hölter Ilona Mossbrugger Julia Calzada-Wack Valentina Strecker Ilka Wittig Iulia Dumitru Tina Wenz Andreas Bender Michaela Aichler Dirk Janik Frauke Neff Axel Walch Leticia Quintanilla-Fend Thomas Floss Raffi Bekeredjian Valérie Gailus-Durner Helmut Fuchs Wolfgang Wurst Thomas Meitinger Holger Prokisch Martin Hrabě de Angelis Thomas Klopstock

Recently, mutations in the mitochondrial translation optimization factor 1 gene (MTO1) were identified as causative in children with hypertrophic cardiomyopathy, lactic acidosis and respiratory chain defect. Here, we describe an MTO1-deficient mouse model generated by gene trap mutagenesis that mirrors the human phenotype remarkably well. As in patients, the most prominent signs and symptoms we...

1999
E Arbustini E Porcu O Bellini M Grasso A Pilotto B Dal Bello P Morbini M Diegoli A Gavazzi G Specchia L Tavazzi

Enteroviral RNA detection in myocarditis and dilated cardiomyopathy is rare. Enteroviral particles and RNA have recently been identified in patient’s skeletal muscle, suggesting that skeletal more than heart muscle hosts the virus in chronic infection. Enteroviral RNA and virus-like particles were found in the myocardium and in the skeletal muscle of two patients with fatal myocarditis: a 39 ye...

2018
James J. O'Byrne Maja Tarailo-Graovac Aisha Ghani Michael Champion Charu Deshpande Ali Dursun Riza K. Ozgul Peter Freisinger Ian Garber Tobias B. Haack Rita Horvath Ivo Barić Ralf A. Husain Leo A.J. Kluijtmans Urania Kotzaeridou Andrew A. Morris Colin J. Ross Saikat Santra Jan Smeitink Mark Tarnopolsky Saskia B. Wortmann Johannes A. Mayr Michaela Brunner-Krainz Holger Prokisch Wyeth W. Wasserman Ron A. Wevers Udo F. Engelke Richard J. Rodenburg Teck Wah Ting Robert McFarland Robert W. Taylor Ramona Salvarinova Clara D.M. van Karnebeek

BACKGROUND Mitochondrial diseases, a group of multi-systemic disorders often characterized by tissue-specific phenotypes, are usually progressive and fatal disorders resulting from defects in oxidative phosphorylation. MTO1 (Mitochondrial tRNA Translation Optimization 1), an evolutionarily conserved protein expressed in high-energy demand tissues has been linked to human early-onset combined ox...

Journal: :archives of cardiovascular imaging 0
zahra ojaghi haghighi department of cardiovascular medicine, echocardiography research center, rajaie cardiovascular, medical and research center, iran university of medical sciences, tehran, ir iran azin alizadehasl department of cardiovascular medicine, echocardiography research center, rajaie cardiovascular, medical and research center, iran university of medical sciences, tehran, ir iran; department of cardiovascular medicine, rajaie cardiovascular, medical and research center, iran university of medical sciences, tehran, ir iran. tel: +98-2123922190, fax: +98-2122663293 hassan moladoust cardiovascular research center, heshmat hospital, school of medicine, guilan university of medical sciences, rasht, ir iran maryam ardeshiri rajaie cardiovascular medical and research center, iran university of medical sciences, tehran, ir iran atousa mostafavi shariati hospital, tehran university of medical sciences, tehran, ir iran nahid rezaeiyan department of cardiovascular medicine, echocardiography research center, rajaie cardiovascular, medical and research center, iran university of medical sciences, tehran, ir iran

conclusions lv twist, torsion and untwist and also rate of them are significantly impaired in dcm and this impairment is well-related to lv global systolic and diastolic dysfunction. vvi is a new noninvasive technique that can be used to evaluate lv torsional parameters. results lv twist value (5.54 ± 1.94° in dcm vs. 11.5 ± 2.45° in control group) and also lv torsion (0.71 ± 0.28°/cm in dcm vs...

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