Clinical and Genotype Characteristics and Symptom Migration in Patients With Mixed Phenotype Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey
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Published:2023-12-20
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ISSN:2193-8261
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Container-title:Cardiology and Therapy
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language:en
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Short-container-title:Cardiol Ther
Author:
González-Moreno Juan, Dispenzieri Angela, Grogan Martha, Coelho Teresa, Tournev Ivailo, Waddington-Cruz Márcia, Wixner JonasORCID, Diemberger Igor, Garcia-Pavia Pablo, Chapman Doug, Gupta Pritam, Glass Oliver, Amass Leslie, Plante-Bordeneuve Violaine, Conceicao Isabel, Jeon Eun-Seok, Maurer Mathew, Costello Jose Gonzalez, Lairez Olivier, Ueda Mitsuharu, Kristen Arnt, Sekijima Yoshiki, Drachman Brian, Slosky David, Hüsing-Kabar Anna, Briseno Maria Alejandra Gonzalez Duarte, Freimer Miriam, Luigetti Marco, Lenihan Daniel, Polydefkis Michael, Hanna Mazen, Nienhuis Hans, Gottlieb Stephen, Nicolau Jose Nativi, Inamo Jocelyn, Emdin Michele, Azevedo Olga, Brunkhorst Robert, Miller Edward, Warner Alberta, Barroso Fabio Adrian, Press Rayomand, Hummel Scott, Beamud Francisco Munoz, Mazzeo Anna, Gentile Luca, Low Soon Chai, Badelita Sorina, Quan Dianna, Tauras James, Zivkovic Sasa, Van Cleemput Johan, Moelgaard Henning, Plana Josep Maria Campistol, Torrón Roberto Fernandéz, Sarswat Nitasha, Murali Srinivas, Mueller Christopher, Fine Nowell, Darstein Felix, Adams David, Dori Amir, Obici Laura, Cirami Calogero Lino, Misawa Sonoko, Shah Sanjiv, Tschoepe Carsten, Davila Lucia Galan, Oh Jeeyoung, Parman Yesim, Marburger Tessa, Ralph Jeffrey,
Publisher
Springer Science and Business Media LLC
Subject
Cardiology and Cardiovascular Medicine
Reference31 articles.
1. Ando Y, Coelho T, Berk JL, Cruz MW, Ericzon BG, Ikeda S, et al. Guideline of transthyretin-related hereditary amyloidosis for clinicians. Orphanet J Rare Dis. 2013;8:31. 2. Gertz MA, Benson MD, Dyck PJ, Grogan M, Coelho T, Cruz M, et al. Diagnosis, prognosis, and therapy of transthyretin amyloidosis. J Am Coll Cardiol. 2015;66(21):2451–66. 3. Adams D, Ando Y, Beirao JM, Coelho T, Gertz MA, Gillmore JD, et al. Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy. J Neurol. 2021;268(6):2109–22. 4. Rowczenio D, Wechalekar A. Mutations in hereditary amyloidosis 2015. Available from: http://amyloidosismutations.com/mut-attr.php Accessed 1 June 2023. 5. Dispenzieri A, Coelho T, Conceicao I, Waddington-Cruz M, Wixner J, Kristen AV, et al. Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update. Orphanet J Rare Dis. 2022;17(1):236.
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