Hepatic amyloidosis (Primary [AL], immunoglobulin light chain): The natural history in 80 patients
- 1 July 1988
- journal article
- research article
- Published by Elsevier in The American Journal of Medicine
- Vol. 85 (1) , 73-80
- https://doi.org/10.1016/0002-9343(88)90505-0
Abstract
No abstract availableKeywords
This publication has 47 references indexed in Scilit:
- Severe Intrahepatic Cholestasis and Rapidly Progressive Renal Failure in a Patient with Immunocyte-Related AmyloidosisJournal of Clinical Gastroenterology, 1987
- Response of Primary Hepatic Amyloidosis to Melphalan and Prednisone: A Case Report and Review of the LiteratureMayo Clinic Proceedings, 1986
- Obstructive jaundice from hepatic amyloidosis in a patient with multiple myelomaAmerican Journal of Hematology, 1985
- Prolongation of Thrombin and Reptilase Times in Patients With Amyloidosis and Acquired Factor X DeficiencySouthern Medical Journal, 1984
- Different Morphologic Aspects and Clinical Features in Massive Hepatic AmyloidosisDigestion, 1984
- Factor‐X deficiency in amyloidosis: A critical reviewAmerican Journal of Hematology, 1981
- Huge Hepatomegaly, Jaundice and Portal Hypertension due to Amyloidosis of the LiverDigestion, 1980
- Acquired Dysfibrinogenaemia in Acute and Chronic Liver DiseaseBritish Journal of Haematology, 1977
- Manifestations of systemic light chain depositionThe American Journal of Medicine, 1976
- The Liver in AmyloidosisDigestion, 1974