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Amyloid
The Journal of Protein Folding Disorders
Volume 26, 2019 - Issue 4
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Articles

A comprehensive safety profile of tafamidis in patients with transthyretin amyloid polyneuropathy

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Pages 203-209 | Received 14 Nov 2018, Accepted 09 Jul 2019, Published online: 27 Jul 2019

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Read on this site (3)

Catarina Falcão de Campos & Isabel Conceição. (2023) Updated Evaluation of the Safety, Efficacy and Tolerability of Tafamidis in the Treatment of Hereditary Transthyretin Amyloid Polyneuropathy. Drug, Healthcare and Patient Safety 15, pages 51-62.
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Arianna Burton, Adam Castaño, Marianna Bruno, Steve Riley, Jennifer Schumacher, Marla B Sultan, Sandi See Tai, Daniel P Judge, Jignesh K Patel & Jeffery W Kelly. (2021) Drug Discovery and Development in Rare Diseases: Taking a Closer Look at the Tafamidis Story. Drug Design, Development and Therapy 15, pages 1225-1243.
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Matthias N. Ungerer, Ernst Hund, Jan C. Purrucker, Laura Huber, Christoph Kimmich, Fabian aus dem Siepen, Selina Hein, Arnt V. Kristen, Katrin Hinderhofer, Jennifer Kollmer, Stefan Schönland, Ute Hegenbart & Markus Weiler. (2021) Real-world outcomes in non-endemic hereditary transthyretin amyloidosis with polyneuropathy: a 20-year German single-referral centre experience. Amyloid 28:2, pages 91-99.
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Articles from other publishers (10)

Deandre King, K. H. Vincent Lau & Michelle C. Kaku. (2023) Treatment Updates for Neuropathy in Hereditary Transthyretin Amyloidosis. Current Treatment Options in Neurology 25:6, pages 137-149.
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G. Chandrasekhar & R. Rajasekaran. (2023) Theoretical investigations of TTR derived aggregation-prone peptides’ potential to biochemically attenuate the amyloidogenic propensities of V30 M TTR amyloid fibrils. Journal of the Indian Chemical Society 100:2, pages 100892.
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Fabio Mastrocola, Frank Nunes & Paulo Sgobbi. 2023. Amyloidosis and Fabry Disease. Amyloidosis and Fabry Disease 235 276 .
Amirthalingam Mohankumar, Duraisamy Kalaiselvi, Govindhan Thiruppathi, Sivaramakrishnan Muthusaravanan, Subramaniam Vijayakumar, Rahul Suresh, Shinkichi Tawata & Palanisamy Sundararaj. (2022) Santalol Isomers Inhibit Transthyretin Amyloidogenesis and Associated Pathologies in Caenorhabditis elegans. Frontiers in Pharmacology 13.
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Laura Obici & Roberta Mussinelli. (2021) Current and Emerging Therapies for Hereditary Transthyretin Amyloidosis: Strides Towards a Brighter Future. Neurotherapeutics 18:4, pages 2286-2302.
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Muneeb Ullah, Abdul Wahab, Sumbul Saeed, Shahid Ullah Khan, Haider Ali, Shah Humayun, Banzeer Ahsan Abbasi, Shah Saud, Khalid Naveed, Sher Aslam Khan & Shah Fahad. (2021) Coronavirus and its terrifying inning around the globe: The pharmaceutical cares at the main frontline. Chemosphere 275, pages 129968.
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Meissane Benbrahim, Kelsey Norman, Vaishali Sanchorawala, Omar K Siddiqi & David Hughes. (2021) A review of novel agents and clinical considerations in patients with ATTR cardiac amyloidosis. Journal of Cardiovascular Pharmacology Publish Ahead of Print.
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Evan T. Powers & Jeffery W. Kelly. 2021. Neurotherapeutics in the Era of Translational Medicine. Neurotherapeutics in the Era of Translational Medicine 65 103 .
Laura Obici & David Adams. (2020) Acquired and inherited amyloidosis: Knowledge driving patients' care. Journal of the Peripheral Nervous System 25:2, pages 85-101.
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Jonathan Park, Ugochukwu Egolum, Shanea Parker, Ebony Andrews, David Ombengi & Hua Ling. (2019) Tafamidis: A First-in-Class Transthyretin Stabilizer for Transthyretin Amyloid Cardiomyopathy. Annals of Pharmacotherapy 54:5, pages 470-477.
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