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Lysozyme Amyloidosis

Published:2006-01 Issue:1 Volume:85 Page:66-73
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Granel Brigitte,Valleix Sophie,Serratrice Jacques,Chérin Patrick,Texeira Antonio,Disdier Patrick,Weiller Pierre-Jean,Grateau Gilles

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference34 articles.

1. Transthyretin familial amyloidotic polyneuropathy: histopathological study of the explanted livers.;Amante;Ann Hepatol,2003

2. The hereditary amyloidoses.;Benson;Best Pract Res Clin Rheumatol,2003

3. A novel variant of human lysozyme (T70N) is common in the normal population.;Booth;Hum Mutat,2000

4. Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis.;Booth;Nature,1997

5. Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene.;Booth;J Clin Invest,1996

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1. Systemic diseases affecting the GI tract: A review of clinical and histopathologic manifestations;Annals of Diagnostic Pathology;2024-12

2. 2024 Update on Classification, Etiology, and Typing of Renal Amyloidosis: A Review;American Journal of Kidney Diseases;2024-09

3. Non-Immunoglobulin Amyloidosis-Mediated Kidney Disease: Emerging Understanding of Underdiagnosed Entities;Advances in Kidney Disease and Health;2024-07

4. Advancing Renal Amyloidosis Care: The Role of Modern Diagnostic Techniques with the Potential of Enhancing Patient Outcomes;International Journal of Molecular Sciences;2024-05-28

5. Bullous Amyloidosis as a cutaneous feature of Familial Lysozyme Amyloidosis;Australasian Journal of Dermatology;2024-03-19

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