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Merlini G, Bellotti V. Molecular mechanisms of amyloidosis. N Engl J Med 349: 583-596, 2003.","DOI":"10.1056\/NEJMra023144"},{"key":"2","unstructured":"2. Kyle RA, Gertz MA. Primary systemic amyloidosis: clinical and laboratory features in 474 cases. Semin Hematol 32: 45-59, 1995."},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Gertz MA. Immunoglobulin light chain amyloidosis: 2014 update on diagnosis, prognosis, and treatment. Am J Hematol 89: 1132-1140, 2014.","DOI":"10.1002\/ajh.23828"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Palladini G, Dispenzieri A, Gertz MA, et al. New criteria for response to treatment in immunoglobulin light chain amyloidosis based on free light chain measurement and cardiac biomarkers: impact on survival outcomes. J Clin Oncol 30: 4541-4549, 2012.","DOI":"10.1200\/JCO.2011.37.7614"},{"key":"5","doi-asserted-by":"publisher","unstructured":"5. Wechalekar AD, Schonland SO, Kastritis E, et al. 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Primary amyloidosis with spontaneous splenic rupture, cholestasis, and liver failure treated with emergency liver transplantation. Am J Gastroenterol 93: 2254-2256, 1998.","DOI":"10.1016\/S0002-9270(98)00509-7"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Nowak G, Westermark P, Wernerson A, Herlenius G, Sletten K, Ericzon BG. Liver transplantation as rescue treatment in a patient with primary AL kappa amyloidosis. Transpl Int 13: 92-97, 2000.","DOI":"10.1111\/j.1432-2277.2000.tb01047.x"},{"key":"10","unstructured":"10. Takano K, Sato Y, Yamamoto S, et al. [A case with primary hepatic amyloidosis accompanied by renal failure treated by living-donor partial liver transplantation]. Ishoku (Japanese Journal of Transplantation) 36 (Suppl): 276, 2001 (in Japanese)."},{"key":"11","doi-asserted-by":"publisher","unstructured":"11. Kumar KS, Lefkowitch J, Russo MW, et al. Successful sequential liver and stem cell transplantation for hepatic failure due to primary AL amyloidosis. 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Treatment of hepatic amyloid light-chain amyloidosis with bortezomib and dexamethasone in a liver transplant patient. Hepatol Res 45: E150-E155, 2015.","DOI":"10.1111\/hepr.12462"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Park MA, Mueller PS, Kyle RA, Larson DR, Plevak MF, Gertz MA. Primary (AL) hepatic amyloidosis: clinical features and natural history in 98 patients. Medicine (Baltimore) 82: 291-298, 2003.","DOI":"10.1097\/01.md.0000091183.93122.c7"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Kumar S, Dispenzieri A, Lacy MQ, et al. Revised prognostic staging system for light chain amyloidosis incorporating cardiac biomarkers and serum free light chain measurements. J Clin Oncol 30: 989-995, 2012.","DOI":"10.1200\/JCO.2011.38.5724"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Gertz MA, Comenzo R, Falk RH, et al. 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