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Extra resources for Amyloidosis - Mechanisms and Prospects for Therapy
The prevalence of clinical amyloidosis is likely to be lower, however, as it probably reflects differences in RA treatments and in genetic backgrounds. AA amyloid deposits primarily target the kidneys, liver, and spleen, and AA amyloidosis becomes clinically overt mainly when renal damage occurs, manifesting as proteinuria, nephrotic syndrome, or impaired renal function. Proteinuria is the clinical sign that most often leads to diagnosis of AA amyloidosis in RA patients. Diagnosis must be based on histological examination of tissue specimen, such as from upper GI or rectal biopsy.
2005). Specific ion effects on the water solubility of macromolecules: PNIPAM and the Hofmeister series. J Am Chem Soc 127,41: 14505-10. , Carter, S. A. and Fink, A. L. (2004). Annular oligomeric amyloid intermediates observed by in situ atomic force microscopy. J Biol Chem 279,23: 24452-9. , Souillac, P. , Carter, S. A. and Fink, A. L. (2002). Surfacecatalyzed amyloid fibril formation. J Biol Chem 277,52: 50914-22. 2 Amyloid A Amyloidosis Secondary to Rheumatoid Arthritis Tadashi Nakamura Kumamoto Center for Arthritis and Rheumatology, and Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan 1.
A. and Edwards, W. D. (2007). Deposition of amyloid proteins in the epicardial coronary arteries of 58 patients with primary systemic amyloidosis. Cardiovasc Pathol 16,2: 75-8. , Bergbreiter, D. E. and Cremer, P. S. (2005). Specific ion effects on the water solubility of macromolecules: PNIPAM and the Hofmeister series. J Am Chem Soc 127,41: 14505-10. , Carter, S. A. and Fink, A. L. (2004). Annular oligomeric amyloid intermediates observed by in situ atomic force microscopy. J Biol Chem 279,23: 24452-9.