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Muscle & Nerve|April 6, 2026
Eplontersen for Hereditary Transthyretin Amyloidosis With Polyneuropathy: An Exploratory Analysis of Treatment Effect in Male and Female PatientsMárcia Waddington Cruz, John L Berk, Yeşim Parman, et al.
Clinical Medicine Insights. Cardiology|May 4, 2026
Best Practices and Key Barriers for Amyloidosis Patient Care at US Specialized Amyloidosis Centers: An Analysis by ARC-ASPIREJose Nativi-Nicolau, Johana Fajardo, Alyssa Galloway, et al.
Muscle & Nerve|November 18, 2024
Estimating Meaningful Differences in Measures of Neuropathic Impairment, Health-Related Quality of Life, and Nutritional Status in Patients With Hereditary Transthyretin AmyloidosisFolke Folkvaljon, Morie Gertz, Julian D Gillmore, et al.
Journal of the American Heart Association|November 22, 2024
Hereditary Transthyretin Amyloidosis in Patients Referred to a Genetic Testing ProgramKunal Bhatt, Diego H Delgado, Sami Khella, et al.
Journal of Neurology|August 14, 2024
Switching from inotersen to eplontersen in patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy: analysis from NEURO-TTRansformIsabel Conceição, John L Berk, Markus Weiler, et al.
Neurology and Therapy|December 16, 2022
Characteristics of Patients with Hereditary Transthyretin Amyloidosis-Polyneuropathy (ATTRv-PN) in NEURO-TTRansform, an Open-label Phase 3 Study of EplontersenTeresa Coelho, Márcia Waddington Cruz, Chi-Chao Chao, et al.
Muscle & Nerve|July 13, 2020
Neuropathy symptom and change: Inotersen treatment of hereditary transthyretin amyloidosisP James B Dyck, Teresa Coelho, Marcia Waddington Cruz, et al.
Journal of Neurology|December 20, 2019
Inotersen preserves or improves quality of life in hereditary transthyretin amyloidosisTeresa Coelho, Aaron Yarlas, Marcia Waddington-Cruz, et al.
JAMA|September 28, 2023
Eplontersen for Hereditary Transthyretin Amyloidosis With PolyneuropathyTeresa Coelho, Wilson Marques, Noel R Dasgupta, et al.
Muscle & Nerve|January 8, 2017
Assessing mNIS+7Ionis and international neurologists' proficiency in a familial amyloidotic polyneuropathy trialPeter J Dyck, John C Kincaid, P James B Dyck, et al.
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