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10.1002/joa3.12021 http://scihub22266oqcxt.onion/10.1002/joa3.12021 C5828272!5828272!29721109     free     free     free Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 233.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       J+Arrhythm 2018 ; 34 (1): 11-22 Nephropedia Template TP {{tp|p=29721109|t=2018. Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice |pdf=|usr=}}{{29721109}} gab.com Text Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice JO: J Arrhythm http://www.kidney.de/pget.php?&tw=1&pmid=29721109 #FOAvip Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited myocardial disease characterized by fibro?fatty replacement of the right ventricular myocardium, and associated with paroxysmal ventricular arrhythmias and sudden cardiac death (SCD). It is currently the second most common cause of SCD after hypertrophic cardiomyopathy in young people <35 years of age, causing up to 20% of deaths in this patient population. This condition has a male preponderance and is more commonly found in individuals of Italian and Greek descent. To date, there is no single diagnostic test for ARVC/D and the diagnosis is made based on clinical, electrocardiographic, and radiological findings according to the Revised 2010 Task Force Criteria. In this review, we will discuss the mainstay treatment which includes pharmacotherapy, implantable cardioverter?defibrillator insertion for abortion of sudden cardiac death, and in the advanced stages of the disease cardiac transplantation. Twit Text FOAVip Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice ????J Arrhythm http://www.kidney.de/pget.php?&tw=1&pmid=29721109 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29721109 #FOAvip English Wikipedia <ref>{{Cite pmid|29721109}}</ref> Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice #MMPMID29721109 Li KHC; Bazoukis G; Liu T; Li G; Wu WKK; Wong SH; Wong WT; Chan YS; Wong MCS; Wassilew K; Vassiliou VS; Tse G J Arrhythm 2018[Feb]; 34 (1): 11-22 PMID29721109show ga Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited myocardial disease characterized by fibro?fatty replacement of the right ventricular myocardium, and associated with paroxysmal ventricular arrhythmias and sudden cardiac death (SCD). It is currently the second most common cause of SCD after hypertrophic cardiomyopathy in young people <35 years of age, causing up to 20% of deaths in this patient population. This condition has a male preponderance and is more commonly found in individuals of Italian and Greek descent. To date, there is no single diagnostic test for ARVC/D and the diagnosis is made based on clinical, electrocardiographic, and radiological findings according to the Revised 2010 Task Force Criteria. In this review, we will discuss the mainstay treatment which includes pharmacotherapy, implantable cardioverter?defibrillator insertion for abortion of sudden cardiac death, and in the advanced stages of the disease cardiac transplantation. äArrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in (epmc).pdf DeepDyve Pubget Overpricing