Immunohistochemical Diagnosis of Amyloid Typing: Utility and Limitations as Determined by Liquid Chromatography-Tandem Mass Spectrometry
Author:
Affiliation:
1. Department of Diagnostic Pathology, Nippon Medical School Hospital
2. Department of Integrated Diagnostic Pathology, Nippon Medical School
3. Department of Molecular Pathology, University of Fukui
Publisher
Medical Association of Nippon Medical School
Link
https://www.jstage.jst.go.jp/article/jnms/91/3/91_JNMS.2024_91-304/_pdf
Reference20 articles.
1. 1. Buxbaum JN, Dispenzieri A, Eisenberg DS, et al. Amyloid nomenclature 2022: update, novel proteins, and recommendations by the International Society of Amyloidosis (ISA) Nomenclature Committee. Amyloid. 2022;29:213-9.
2. 2. Naiki H, Sekijima Y, Ueda M, et al. Human amyloidosis, still intractable but becoming curable: the essential role of pathological diagnosis in the selection of type-specific therapeutics. Pathol Int. 2020;70:191-8.
3. 3. Bulawa CE, Connelly S, Devit M, et al. Tafamidis, a potent and selective transthyretin kinetic stabilizer that inhibits the amyloid cascade. Proc Natl Acad Sci U S A. 2012;109:9629-34.
4. 4. Maurer MS, Schwartz JH, Gundapaneni B, et al. Tafamidis Treatment for patients with transthyretin amyloid cardiomyopathy. N Engl J Med. 2018;379:1007-16.
5. 5. Kastritis E, Palladini G, Minnema MC, et al. Daratumumab-based treatment for immunoglobulin light-chain amyloidosis. N Engl J Med. 2021;385:46-58.
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