Author:
Pepys M. B.,Herbert J.,Hutchinson W. L.,Tennent G. A.,Lachmann H. J.,Gallimore J. R.,Lovat L. B.,Bartfai T.,Alanine A.,Hertel C.,Hoffmann T.,Jakob-Roetne R.,Norcross R. D.,Kemp J. A.,Yamamura K.,Suzuki M.,Taylor G. W.,Murray S.,Thompson D.,Purvis A.,Kolstoe S.,Wood S. P.,Hawkins P. N.
Publisher
Springer Science and Business Media LLC
Reference40 articles.
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2. Pepys, M. B. & Hawkins, P. N. in Samter's Immunologic Diseases (eds Austen, K. F., Frank, M. M., Atkinson, J. P. & Cantor, H.) 401–412 (Lippincott Williams, Philadelphia, 2001)
3. Holmgren, G. et al. Clinical improvement and amyloid regression after liver transplantation in hereditary transthyretin amyloidosis. Lancet 341, 1113–1116 (1993)
4. Gillmore, J. D., Hawkins, P. N. & Pepys, M. B. Amyloidosis: a review of recent diagnostic and therapeutic developments. Brit. J. Haematol. 99, 245–256 (1997)
5. Gillmore, J. D. et al. Curative hepatorenal transplantation in systemic amyloidosis caused by the Glu526Val fibrinogen α-chain variant in an English family. Q. J. Med. 93, 269–275 (2000)
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