Electro-clinical presentation of hereditary transthyretin related amyloidosis when presenting as a polyneuropathy of unknown origin in northern France-Reference-Cited by-同舟云学术

Electro-clinical presentation of hereditary transthyretin related amyloidosis when presenting as a polyneuropathy of unknown origin in northern France

Published:2021-11 Issue:9 Volume:177 Page:1160-1167
ISSN:0035-3787
Container-title:Revue Neurologique
language:en
Short-container-title:Revue Neurologique

Author:

Davion J.-B.,Bocquillon P.,Cassim F.,Frezel N.,Lacour A.,Dhaenens C.-M.,Maurage C.-A.,Gibier J.-B.,Hachulla E.,Nguyen The Tich S.,Defebvre L.,Merle P.-E.,Tard C.

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference19 articles.

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2. Guideline of transthyretin-related hereditary amyloidosis for clinicians;Ando;Orphanet J Rare Dis,2013

3. Tafamidis for transthyretin familial amyloid polyneuropathy: a randomized, controlled trial;Coelho;Neurology,2012

4. Inotersen treatment for patients with hereditary transthyretin amyloidosis;Benson;N Engl J Med,2018

5. Patisiran, an RNAi therapeutic, for hereditary transthyretin amyloidosis;Adams;N Engl J Med,2018

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

2. Phenotypic characteristics of F64L, I68L, I107V, and S77Y ATTRv genotypes from the Transthyretin Amyloidosis Outcomes Survey (THAOS);PLOS ONE;2024-01-19

3. Amyloid-β Effects on Peripheral Nerve: A New Model System;International Journal of Molecular Sciences;2023-09-23

4. Neuropathie amyloïde à transthyrétine : du diagnostic au traitement;Bulletin de l'Académie Nationale de Médecine;2023-05

5. Strategy for genetic analysis in hereditary neuropathy;Revue Neurologique;2023-01