Results 161 to 170 of about 10,856 (192)
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Hereditäre Transthyretin-Amyloidosen
Der Nervenarzt, 2014Hereditary amyloidosis is an autosomal dominant fatal multisystem disease caused by extracellular deposition of misfolded proteins and, therefore represents a hereditary protein folding or deposition disease that leads to progressive organ damage and eventually death.
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Transthyretin amyloid cardiomyopathy
The American Journal of the Medical Sciences, 2023Giuseppe, Famularo, Guido, Ventroni
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Blinded Potency Comparison of Transthyretin Kinetic Stabilisers by Subunit Exchange in Human Plasma
Amyloid: the International Journal of Experimental and Clinical Investigation: the Official Journal of the International Society of Amyloidosis, 2021Evan T Powers, Jeffery W. Kelly, Jin Xu
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Amyloid: the International Journal of Experimental and Clinical Investigation: the Official Journal of the International Society of Amyloidosis, 2022
Carsten Tschöpe +2 more
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Carsten Tschöpe +2 more
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Tafamidis Treatment for Patients With Transthyretin Amyloid Cardiomyopathy
New England Journal of Medicine, 2018Mathew S Maurer +2 more
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Natural History, Quality of Life, and Outcome in Cardiac Transthyretin Amyloidosis
Circulation, 2019Julian D Gillmore +2 more
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Tafamidis: A First-in-Class Transthyretin Stabilizer for Transthyretin Amyloid Cardiomyopathy
Annals of Pharmacotherapy, 2020Hua Ling
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