Hereditary transthyretin amyloidosis: current treatment
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Neurology (clinical),Neurology
Reference36 articles.
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1. A description of variant transthyretin amyloidosis (ATTRv) stage 1 patients and asymptomatic carriers in Spain: the EMPATIa study;Orphanet Journal of Rare Diseases;2024-09-06
2. Recommendations update for the diagnosis and treatment of transthyretin variant amyloidosis (ATTRv);Medicina Clínica (English Edition);2024-09
3. Actualización de las recomendaciones para el diagnóstico y tratamiento de la amiloidosis por transtiretina variante (ATTRv);Medicina Clínica;2024-06
4. Quantitative sensory testing: a good tool to identify subclinical neuropathy in ATTRV30M amyloidosis patients?;Amyloid;2022-12-15
5. A novel TTR mutation (p.Ala65Val) underlying late-onset hereditary transthyretin (ATTRv) amyloidosis with mixed cardiac and neuropathic phenotype: a case report;BMC Neurology;2022-12-09
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