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Archives of Cardiovascular Diseases|June 20, 2012
Circadian rhythm of blood pressure reflects the severity of cardiac impairment in familial amyloid polyneuropathyVincent Algalarrondo, Ludivine Eliahou, Isabelle Thierry, et al.
Eurointervention : Journal of Europcr in Collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology|September 18, 2009
A randomised controlled trial of upstream administration of eptifibatide in patients presenting non-ST segment elevation acute coronary syndrome treated with an invasive strategyEric Durand, Christian W Hamm, Carlos M Macaya, et al.
Medicine|July 25, 2006
Impact of liver transplantation on cardiac autonomic denervation in familial amyloid polyneuropathyNicolas Delahaye, François Rouzet, Laure Sarda, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 16, 2023
Comparison between tafamidis and liver transplantation as first-line therapy for hereditary transthyretin amyloidosisPierre Socie, Anouar Benmalek, Cécile Cauquil, et al.
JACC. Cardiovascular Imaging|November 14, 2016
Cardiac Dysautonomia Predicts Long-Term Survival in Hereditary Transthyretin Amyloidosis After Liver TransplantationVincent Algalarrondo, Teresa Antonini, Marie Théaudin, et al.
Annals of Neurology|September 16, 2015
Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in FranceLouise-Laure Mariani, Pierre Lozeron, Marie Théaudin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 24, 2023
Detailed clinical, physiological and pathological phenotyping can impact access to disease-modifying treatments in ATTR carriersDiane Beauvais, Céline Labeyrie, Cécile Cauquil, et al.
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