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Two types of systemic amyloidosis in a single patient.
Papa R, Gilbertson JA, Rendell N, Wechalekar AD, Gillmore JD, Hawkins PN, Lachmann HJ. Papa R, et al. Among authors: lachmann hj. Amyloid. 2020 Dec;27(4):275-276. doi: 10.1080/13506129.2020.1760238. Epub 2020 May 6. Amyloid. 2020. PMID: 32372654 No abstract available.
Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis.
Aganna E, Martinon F, Hawkins PN, Ross JB, Swan DC, Booth DR, Lachmann HJ, Bybee A, Gaudet R, Woo P, Feighery C, Cotter FE, Thome M, Hitman GA, Tschopp J, McDermott MF. Aganna E, et al. Among authors: lachmann hj. Arthritis Rheum. 2002 Sep;46(9):2445-52. doi: 10.1002/art.10509. Arthritis Rheum. 2002. PMID: 12355493 Free article.
Interleukin-1-receptor antagonist in the Muckle-Wells syndrome.
Hawkins PN, Lachmann HJ, McDermott MF. Hawkins PN, et al. Among authors: lachmann hj. N Engl J Med. 2003 Jun 19;348(25):2583-4. doi: 10.1056/NEJM200306193482523. N Engl J Med. 2003. PMID: 12815153 Free article. No abstract available.
250 results