Late-onset hereditary ATTR V30M amyloidosis with polyneuropathy: Characterization of Brazilian subjects from the THAOS registry-Reference-Cited by-同舟云学术

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Late-onset hereditary ATTR V30M amyloidosis with polyneuropathy: Characterization of Brazilian subjects from the THAOS registry

Published:2019-08 Issue: Volume:403 Page:1-6
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Pinto Marcus Vinicius,Pinto Luiz Felipe,Dias Moises,Rosa Renata Santa,Mundayat Rajiv,Pedrosa Roberto Coury,Waddington-Cruz Marcia

Funder

Pfizer

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference42 articles.

1. Familial amyloid polyneuropathy;Plante-Bordeneuve;Lancet Neurol.,2011

2. Clinical variability in type I familial amyloid polyneuropathy (Val30Met): comparison between late- and early-onset cases in Portugal;Conceicao;Muscle Nerve,2007

3. Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form;Koike;Arch. Neurol.,2002

4. Transthyretin familial amyloid polyneuropathy (TTR-FAP) in Mallorca: a comparison between late- and early-onset disease;Buades-Reines;J. Peripher. Nerv. Syst.,2016

5. Diagnostic hallmarks and pitfalls in late-onset progressive transthyretin-related amyloid-neuropathy;Dohrn;J. Neurol.,2013

Cited by 19 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hereditary transthyretin amyloidosis: a myriad of factors that influence phenotypic variability;Journal of Neurology;2024-06-22

2. Diagnosis and treatment of hereditary transthyretin amyloidosis with polyneuropathy in the United States: Recommendations from a panel of experts;Muscle & Nerve;2024-01-04

3. Syncope and Rhythm Disturbances as Common Clinical Manifestations in Amyloidosis;International Journal of Cardiovascular Sciences;2024

4. A molecular basis for tetramer destabilization and aggregation of transthyretin Ala97Ser;Protein Science;2023-03-24

5. Brazilian consensus for diagnosis, management and treatment of hereditary transthyretin amyloidosis with peripheral neuropathy: second edition;Arquivos de Neuro-Psiquiatria;2023-03

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