Low ECG signals such as QRS complexes are widely considered a marker of cardiac amyloidosis.
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Jnis Vaia < a died on 9 January 2016 aged 46 from cardiac amyloidosis, after struggling with heart problems.
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It was incomplete when its author, Robert Jordan, died on September 16, 2007, from cardiac amyloidosis.
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The patient had developed a rare condition called cardiac amyloidosis, a disease in which the heart is infiltrated by an abnormal protein produced elsewhere in the body.
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Troponins can also indicate several forms of cardiomyopathy, such as dilated cardiomyopathy, hypertrophic cardiomyopathy or ( left ) ventricular hypertrophy, peripartum cardiomyopathy, Takotsubo cardiomyopathy, or infiltrative disorders such as cardiac amyloidosis.
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Types of cardiac amyloidosis include cardiac manifestations of AL amyloidosis and amyloidosis, cardiac manifestations of transthyretin-related hereditary amyloidosis, and isolated atrial amyloidosis, a form of amyloidosis affecting the atria of the heart.
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It was incomplete at the time of the death of [ when ] its author, Robert Jordan, who died on September 16, 2007 from cardiac amyloidosis [, ] having written 50, 000 words.
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The DISCOVERY trial is a screening study evaluating the prevalence of TTR mutations in patients suspected of having cardiac amyloidosis with the goal of identifying and facilitating the diagnosis of FAC . Two Phase III trials are being conducted to evaluate drugs which may block amyloid formation : ENDEAVOUR, evaluating revusiran, an investigational medicine ( this study has been halted ), in the treatment of familial TTR-induced cardiomyopathy, and ATTR-ACT, evaluating tafamidis in the treatment of TTR-induced cardiomyopathy.
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