Familial amyloid polyneuropathy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Neurology
Reference42 articles.
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2. Frequencies and geographic distributions of genetic mutations in transthyretin and nontransthyretin-related familial amyloidosis;Zhen;Clin Genet,2015
3. Clinical features of familial amyloid polyneuropathy carrying transthyretin mutations in four Chinese kindreds;Liu;J Peripher Nerv Syst,2017
4. FAP in India: a first genetically proven case;Pan;Orphanet J Rare Dis,2015
5. A study of the neuropathy associated with transthyretin amyloidosis (ATTR) in the UK;Carr;J Neurol Neurosurg Psychiatry,2016
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1. T2-relaxometry in a large cohort of hereditary transthyretin amyloidosis with polyneuropathy;Amyloid;2024-09-02
2. Serum neurofilament light chain in hereditary transthyretin amyloidosis: validation in real-life practice;Amyloid;2024-02-13
3. Red flags in patients with hereditary transthyretin amyloidosis at diagnosis in a non-endemic area of Spain;Neurología (English Edition);2023-03
4. Functional and morphometric assessment of small-fibre damage in late-onset hereditary transthyretin amyloidosis with polyneuropathy: the controversial relation between small-fibre-related symptoms and diagnostic test findings;Amyloid;2022-09-12
5. Patterns of myelinated nerve fibers loss in transthyretin amyloid polyneuropathy and mimics;Annals of Clinical and Translational Neurology;2022-06-04
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