Recommendations update for the diagnosis and treatment of transthyretin variant amyloidosis (ATTRv)-Reference-Cited by-同舟云学术

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Recommendations update for the diagnosis and treatment of transthyretin variant amyloidosis (ATTRv)

Published:2024-09 Issue: Volume: Page:
ISSN:2387-0206
Container-title:Medicina Clínica (English Edition)
language:en
Short-container-title:Medicina Clínica (English Edition)

Author:

González-Moreno Juan,Galán Dávila Lucía,Gonzalez-Lopez Esther,Conceiçao Isabel,Barriales-Villa Roberto,Falcão de Campos Catarina,Cardoso Márcio Neves,Casasnovas Carlos,Fernández-Martín Julián,Morales Raúl Juntas,López Inés Losada,Martínez-Vicente Laura,Muñoz-Beamud Francisco,Quintana Luis F.,Sevilla Teresa

Publisher

Elsevier BV

Reference31 articles.

1. Transthyretin (ATTR) amyloidosis: clinical spectrum, molecular pathogenesis and disease-modifying treatments;Sekijima;J Neurol Neurosurg Psychiatry,2015

2. Epidemiological and clinical characteristics of persons with transthyretin hereditary amyloid polyneuropathy: a global synthesis of 532 cases;Cruz;Amyloid,2017

3. Amyloid nomenclature 2022: update, novel proteins, and recommendations by the International Society of Amyloidosis (ISA) Nomenclature Committee;Buxbaum;Amyloid,2022

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

5. Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations;Conceição;Amyloid,2019

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