Journal Report

Amyloid

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Journal Information
Journal Title
Amyloid
Publisher
Taylor and Francis Ltd.
ISSN
1350-6129
E-ISSN
1744-2818
Database
SCOPUS
Domain
Health Sciences, Life Sciences, Physical Sciences, Social Sciences
Classification History
Year A+ A B C
2026 ✓ ✓
2025 ✓ ✓
2024 ✓ ✓
2023 ✓ ✓
2021/2022 ✓ ✓
2020 ✓ ✓
2019 ✓ ✓
2018 ✓
A journal may have more than one classification in the same year. All recorded classifications are displayed.
Recent Articles
Longitudinal changes in gastrointestinal amyloid deposition before and after patisiran treatment in Hereditary ATTR amyloidosis
Shinji Masuko, Mitsuto Sato, Ken Takasone et al.
2026-11-9 Pages 1-11
Amyloid nomenclature 2026: update, novel proteins, and discussion of intracellular aggregates and toxicity. Recommendations by the International Society of Amyloidosis Nomenclature Committee
Joel N. Buxbaum, David S. Eisenberg, Marcus Fändrich et al.
2026-11-8 Pages 1-11
Operational definitions of the asymptomatic <i>TTR</i> variant carrier: a methodological framework for ATTRv amyloidosis polyneuropathy research
Isabel Conceição, José Castro, Mamede de Carvalho
2026-11-3 Pages 1-4
Robert A. Kyle: In Memoriam
Shaji K. Kumar, Morie A. Gertz
2026-11-1 Pages 1-2
Prevalence and prognostic impact of valvular heart disease in transthyretin cardiac amyloidosis
Camille Sarrazyn, Philippe Debonnaire, Mathias Claeys et al.
2026-10-29 Pages 1-13
Ixazomib maintenance for the treatment of light chain AL amyloidosis
Caitlin Sarubbi, Hani Hassoun, Grace Gallagher et al.
2026-10-29 Pages 1-4
Quality standards for the diagnosis and management of ATTR and AL amyloidosis: a nominal group technique study
Laura Obici, Thibaud Damy, Lucia Galan et al.
2026-10-21 Pages 1-15
Multiple musculoskeletal procedures over time and the risk of amyloidosis: a Danish nationwide cohort study
Navid Noory, Peter L. Graversen, Eva Havers-Borgersen et al.
2026-10-20 Pages 1-4
Full-length light chain sequencing refocuses attention on the constant domain in AL amyloidosis
Luis del Pozo-Yauner
2026-10-15 Pages 1-3
Childhood onset, indolent progression, and risk of hepatic rupture: the natural history of hereditary lysozyme amyloidosis
Jack E. Carruthers, Janet A. Gilbertson, Dorota Rowczenio et al.
2026-10-12 Pages 1-9
Articles retrieved from Crossref.
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Printed: November 11, 2026 08:01