Cardiac and peripheral vasomotor autonomic functions in late-onset transthyretin Val30Met familial amyloid polyneuropathy-Reference-Cited by-同舟云学术

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Cardiac and peripheral vasomotor autonomic functions in late-onset transthyretin Val30Met familial amyloid polyneuropathy

Published:2017-10-05 Issue:11 Volume:264 Page:2293-2302
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Koike Haruki,Nakamura Tomohiko,Hashizume Atsushi,Nishi Ryoji,Ikeda Shohei,Kawagashira Yuichi,Iijima Masahiro,Katsuno Masahisa,Sobue Gen

Funder

The Ministry of Health, Labor and Welfare of Japan

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/article/10.1007/s00415-017-8629-2/fulltext.html

Reference41 articles.

1. Ikeda SI, Makishita H, Oguchi K, Yanagisawa N, Nagata T (1982) Gastrointestinal amyloid deposition in familial amyloid polyneuropathy. Neurology 32:1364–1368

2. Ando Y, Nakamura M, Araki S (2005) Transthyretin-related familial amyloidotic polyneuropathy. Arch Neurol 62:1057–1062

3. Benson MD, Kincaid JC (2007) The molecular biology and clinical features of amyloid neuropathy. Muscle Nerve 36:411–423

4. Planté-Bordeneuve V, Said G (2011) Familial amyloid polyneuropathy. Lancet Neurol 10:1086–1097

5. Sekijima Y (2015) Transthyretin (ATTR) amyloidosis: clinical spectrum, molecular pathogenesis and disease-modifying treatments. J Neurol Neurosurg Psychiatry 86:1036–1043

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1. Cardiovascular autonomic failure in hereditary transthyretin amyloidosis and TTR carriers is an early and progressive disease marker;Clinical Autonomic Research;2024-05-20

2. Cardiovascular autonomic failure in hereditary transthyretin amyloidosis and TTR carriers is an early and progressive disease marker;2024-03-07

3. 2023 Expert Consensus of the Taiwan Society of Cardiology on the Diagnosis and Treatment of Cardiac Amyloidosis;ACTA CARDIOL SIN;2023

4. The Silent Period for Small Fiber Sensory Neuropathy Assessment in a Mixed Cohort of Transthyretin-Mediated Amyloidosis;Biomedicines;2022-08-24

5. Expert opinion on monitoring symptomatic hereditary transthyretin-mediated amyloidosis and assessment of disease progression;Orphanet Journal of Rare Diseases;2021-10-03

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