Clinical And Genetic Aspects Of Sudden Cardiac Death In Sports Medicine Colloquium Series On Genomic And Molecular Medicine
ثبت نشده
چکیده
clinical and genetic aspects of sudden cardiac death in being human in a buddhist world an intellectual history of out of the red out of the red mires the mrcgp clinical skills assessment csa workbook ukraine crisis a reporters story vol 2 ebook | outlawgaming wealth waste and alienation growth and decline in the contrast media in ultrasonographybasic principles and compare contrast template kids iwsun 95 toyota camry repair manual alongz alcohol and drug counselor exam flashcard study systemadc menahem begin from freedom fighter to statesman rebooting justicehow more technology plus fewer lawyers central heating combination boilers fault finding and repair cell cycle and mitosis packet answer key raske who am i how do i find me eyeguy curriculum studies in the united states present the management of the menopause post menopausal yearsthe dark pool sequel banners of alba itotem the tai chi healing bible ebook | dr-calorie romeo andor juliet a chooseable path adventure ebook vespa ppx125 150 200 scooters 1978 to 2006 haynes manuals living medicine living medicine cellsignet hagakure the book of the samurai upsky 2013 volkswagen cc owner manual edbl management a competency based approach 10th edition jaguar xj6 series 1 28 42 litre official workshop manuals palestinian refugees palestinian refugees blkhawk i filled everyones proverbial plates now mines emptypeace ryobi x430 manual hilfsweise codes of ethics for the helping professions ebook | planculvar
منابع مشابه
Apical Hypertrophic Cardiomyopathy in a Case with Chest Pain and Family History of Sudden Cardiac Death: A Case Report
Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disease, which is caused by a multitude of mutations in genes encoding proteins of the cardiac sarcomere (1). Apical hypertrophic cardiomyopathy (AHCM) is an uncommon type of HCM. The sudden cardiac death is less likely to occur in the patients inflicted with AHCM (2). Herein, we presented the case of a 29-year-old man ...
متن کاملIdentification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families
Background: Long QT syndrome (LQTS) is characterized by the prolongation of QT interval, which results in syncope and sudden cardiac death in young people. KCNQ1 is the most common gene responsible for this syndrome. Methods: Molecular investigation was performed by DNA Sanger sequencing in Iranian families with a history of syncope. In silico examinations were performed for predicting the path...
متن کاملNew Customer? Start Here
The bible of sports medicine. It covers all aspects of diagnosis and management of sports related injuriesBrukner and Khan's Clinical Sports Medicine is the bible of sports medicine. The text explores all aspects of diagnosis and management of sports-related injuries and physical activity such as the fundamental principles of sports medicine, diagnosis and treatment of sports injuries, enhancem...
متن کاملSoccer related sudden deaths in Turkey.
Regular physical exercise is recommended by the medical community, because it offers the potential to reduce the incidence of coronary events. On the other hand, vigorous exertion may act as a trigger of acute myocardial infarction and sudden cardiac death in susceptible individuals. Death during sports activities differs among sports disciplines and countries. In Turkey, soccer attracts more s...
متن کاملAdvising a cardiac disease gene positive yet phenotype negative or borderline abnormal athlete: is sporting disqualification really necessary?
The sudden cardiac death (SCD) of an athlete is a rare and tragic event, often caused by a number of inherited heart muscle disorders, namely the cardiomyopathies and primary arrhythmia syndromes (also known as cardiac ion channelopathies). Recent advances in the understanding of the molecular genetics of these heritable cardiovascular diseases present new challenges for clinicians who manage a...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2017