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Showing results (501-510 of 537) with videos related to

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Annals of Internal Medicine|January 22, 2004
High-dose melphalan and autologous stem-cell transplantation in patients with AL amyloidosis: an 8-year studyMartha Skinner, Vaishali Sanchorawala, David C Seldin, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|April 8, 2019
Early Detection of Multiorgan Light-Chain Amyloidosis by Whole-Body <sup>18</sup>F-Florbetapir PET/CTEric C Ehman, M Samir El-Sady, Marie F Kijewski, et al.
JACC. Cardiovascular Imaging|August 20, 2018
Relative Apical Sparing of Myocardial Longitudinal Strain Is Explained by Regional Differences in Total Amyloid Mass Rather Than the Proportion of Amyloid DepositsPaco E Bravo, Kana Fujikura, Marie Foley Kijewski, et al.
Circulation. Cardiovascular Imaging|November 15, 2022
Optimal Echocardiographic Parameters to Improve the Diagnostic Yield of Tc-99m-Bone Avid Tracer Cardiac Scintigraphy for Transthyretin Cardiac AmyloidosisSarah Am Cuddy, Yesh Datar, Gavin Ovsak, et al.
JACC. Heart Failure|September 7, 2024
Functional Status and Quality of Life in Light-Chain Amyloidosis: Advanced Imaging, Longitudinal Changes, and OutcomesOlivier F Clerc, Shilpa Vijayakumar, Sarah A M Cuddy, et al.
Cardiovascular Drugs and Therapy|February 17, 2020
Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR)Daniel P Judge, Arnt V Kristen, Martha Grogan, et al.
Cardiovascular Drugs and Therapy|June 18, 2020
Correction to: Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR)Daniel P Judge, Arnt V Kristen, Martha Grogan, et al.
Medrxiv : the Preprint Server for Health Sciences|September 25, 2023
Prognostic Value of Left Ventricular <sup>18</sup> F-Florbetapir Uptake in Systemic Light-Chain AmyloidosisOlivier F Clerc, Yesh Datar, Sarah Am Cuddy, et al.
JACC. Cardiovascular Imaging|December 19, 2021
Myocardial Composition in Light-Chain Cardiac Amyloidosis More Than 1 Year After Successful TherapySarah A M Cuddy, Michael Jerosch-Herold, Rodney H Falk, et al.
JACC. Cardiovascular Imaging|July 13, 2024
Prognostic Value of Left Ventricular <sup>18</sup>F-Florbetapir Uptake in Systemic Light-Chain AmyloidosisOlivier F Clerc, Yesh Datar, Sarah A M Cuddy, et al.
Pageof 54

Showing results (501-510 of 537) with videos related to

Sort By:
Pageof 54
Annals of Internal Medicine|January 22, 2004
High-dose melphalan and autologous stem-cell transplantation in patients with AL amyloidosis: an 8-year studyMartha Skinner, Vaishali Sanchorawala, David C Seldin, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|April 8, 2019
Early Detection of Multiorgan Light-Chain Amyloidosis by Whole-Body <sup>18</sup>F-Florbetapir PET/CTEric C Ehman, M Samir El-Sady, Marie F Kijewski, et al.
JACC. Cardiovascular Imaging|August 20, 2018
Relative Apical Sparing of Myocardial Longitudinal Strain Is Explained by Regional Differences in Total Amyloid Mass Rather Than the Proportion of Amyloid DepositsPaco E Bravo, Kana Fujikura, Marie Foley Kijewski, et al.
Circulation. Cardiovascular Imaging|November 15, 2022
Optimal Echocardiographic Parameters to Improve the Diagnostic Yield of Tc-99m-Bone Avid Tracer Cardiac Scintigraphy for Transthyretin Cardiac AmyloidosisSarah Am Cuddy, Yesh Datar, Gavin Ovsak, et al.
JACC. Heart Failure|September 7, 2024
Functional Status and Quality of Life in Light-Chain Amyloidosis: Advanced Imaging, Longitudinal Changes, and OutcomesOlivier F Clerc, Shilpa Vijayakumar, Sarah A M Cuddy, et al.
Cardiovascular Drugs and Therapy|February 17, 2020
Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR)Daniel P Judge, Arnt V Kristen, Martha Grogan, et al.
Cardiovascular Drugs and Therapy|June 18, 2020
Correction to: Phase 3 Multicenter Study of Revusiran in Patients with Hereditary Transthyretin-Mediated (hATTR) Amyloidosis with Cardiomyopathy (ENDEAVOUR)Daniel P Judge, Arnt V Kristen, Martha Grogan, et al.
Medrxiv : the Preprint Server for Health Sciences|September 25, 2023
Prognostic Value of Left Ventricular <sup>18</sup> F-Florbetapir Uptake in Systemic Light-Chain AmyloidosisOlivier F Clerc, Yesh Datar, Sarah Am Cuddy, et al.
JACC. Cardiovascular Imaging|December 19, 2021
Myocardial Composition in Light-Chain Cardiac Amyloidosis More Than 1 Year After Successful TherapySarah A M Cuddy, Michael Jerosch-Herold, Rodney H Falk, et al.
JACC. Cardiovascular Imaging|July 13, 2024
Prognostic Value of Left Ventricular <sup>18</sup>F-Florbetapir Uptake in Systemic Light-Chain AmyloidosisOlivier F Clerc, Yesh Datar, Sarah A M Cuddy, et al.
Pageof 54