Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas-Reference-Cited by-同舟云学术

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Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas

Published:2012-01-06 Issue:2 Volume:83 Page:152-158
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:J Neurol Neurosurg Psychiatry

Author:

Koike Haruki,Tanaka Fumiaki,Hashimoto Rina,Tomita Minoru,Kawagashira Yuichi,Iijima Masahiro,Fujitake Junko,Kawanami Toru,Kato Takeo,Yamamoto Masahiko,Sobue Gen

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Cited by 174 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. Clinical and biochemical characterization of asymptomatic carriers and symptomatic patients with hereditary transthyretin amyloidosis caused by TTR V30L mutation;Neurological Sciences;2024-09-14

2. Transthyretin amyloid polyneuropathy in France: A cross-sectional study with 413 patients and real-world tafamidis meglumine use (2009–2019);Revue Neurologique;2024-09

3. Diflunisal versus tafamidis on neuropathy and cardiomyopathy in hereditary transthyretin amyloidosis;Annals of Clinical and Translational Neurology;2024-08-02

4. Altered connectivity of central autonomic network: effects of dysautonomia in hereditary transthyretin amyloidosis with polyneuropathy;Amyloid;2024-07-24

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

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