Citations (14)
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Sara Cavaco, Ana Martins da Silva, Joana Fernandes, Ana Paula Sousa, Cristina Alves, Márcio Cardoso, Armando Teixeira-Pinto & Teresa Coelho. (2023) Predictors of cognitive dysfunction in hereditary transthyretin amyloidosis with liver transplant. Amyloid 30:1, pages 119-126.
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Shun Wang, Jingping Sun, Qun Lu, Hao Li & Yun Zhang. (2022) Late-Onset Hereditary Transthyretin Amyloidosis Val30Met in an Elderly Person in a Non-Endemic Area. International Medical Case Reports Journal 15, pages 299-306.
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Articles from other publishers (12)
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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Marcus Vinicius Pinto, Marcondes Cavalcante FrançaJrJr, Marcus Vinicius Magno Gonçalves, Marcela Câmara Machado-Costa, Marcos Raimundo Gomes de Freitas, Francisco de Assis Aquino Gondim, Carlo Domenico Marrone, Alberto Rolim Muro Martinez, Carolina Lavigne Moreira, Osvaldo J. M. Nascimento, Anna Paula Paranhos Covaleski, Acary Souza Bulle de Oliveira, Camila Castelo Branco Pupe, Marcia Maria Jardim Rodrigues, Francisco Tellechea Rotta, Rosana Herminia Scola, Wilson MarquesJrJr & Márcia Waddington-Cruz. (2023) Brazilian consensus for diagnosis, management and treatment of hereditary transthyretin amyloidosis with peripheral neuropathy: second edition. Arquivos de Neuro-Psiquiatria 81:03, pages 308-321.
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Inés Asunción Losada-López, Solange Kapetanovic-García, Teresa Sevilla-Mantecón & Francisco Muñoz-Beamud. (2023) Follow-up regimens for carriers of hereditary transthyretin variants. Medicina Clínica 160:5, pages 213-217.
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Inés Asunción Losada-López, Solange Kapetanovic-García, Teresa Sevilla-Mantecón & Francisco Muñoz-Beamud. (2023) Follow-up regimens for carriers of hereditary transthyretin variants. Medicina Clínica (English Edition) 160:5, pages 213-217.
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Sriram Easwaran, Milind Phadke, Nitin Burkule, Ashwin Dalal & Pratap Nathani. (2023) A case of fatal familial edema. IHJ Cardiovascular Case Reports (CVCR) 7:1, pages 29-32.
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Michael F. Murray, Muin J. Khoury & Noura S. Abul-Husn. (2022) Addressing the routine failure to clinically identify monogenic cases of common disease. Genome Medicine 14:1.
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Thomas H. Brannagan3rd3rd, John L. Berk, Julian D. Gillmore, Mathew S. Maurer, Márcia Waddington‐Cruz, Marianna Fontana, Ahmad Masri, Laura Obici, Michela Brambatti, Brenda F. Baker, Lisa A. Hannan, Gustavo Buchele, Nick J. Viney, Teresa Coelho & Jose Nativi‐Nicolau. (2022)
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Anvesh K. R. Dasari, Sujung Yi, Matthew F. Coats, Sungsool Wi & Kwang Hun Lim. (2022) Toxic Misfolded Transthyretin Oligomers with Different Molecular Conformations Formed through Distinct Oligomerization Pathways. Biochemistry 61:21, pages 2358-2365.
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Chafic Karam, Duncan Brown, Min Yang, Nicolae Done, Jing Jing Zhu, Alexandra Greatsinger, Ana Bozas, Montserrat Vera‐Llonch & James Signorovitch. (2022)
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José Castro, Bruno Miranda, Isabel de Castro & Isabel Conceição. (2021) Changes in nerve conduction studies predate clinical symptoms onset in early onset Val30Met hereditary ATTR amyloidosis. European Journal of Neurology 29:3, pages 826-832.
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Haruki Koike, Takahiro Okumura, Toyoaki Murohara & Masahisa Katsuno. (2021) Multidisciplinary Approaches for Transthyretin Amyloidosis. Cardiology and Therapy 10:2, pages 289-311.
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Csilla Andrea Eötvös, Giorgia Pastiu, Iulia Zehan, Cerasela Goidescu, Roxana Chiorescu, Roxana Lazar, Florina Frîngu, Raluca Tomoaia, Monica Pop, Adrian Molnar, Sorin Pop & Dan Blendea. 2021. Cardiomyopathy - Disease of the Heart Muscle. Cardiomyopathy - Disease of the Heart Muscle.