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Guidelines on the diagnosis and investigation of AL amyloidosis.
Gillmore JD, Wechalekar A, Bird J, Cavenagh J, Hawkins S, Kazmi M, Lachmann HJ, Hawkins PN, Pratt G; BCSH Committee. Gillmore JD, et al. Among authors: lachmann hj. Br J Haematol. 2015 Jan;168(2):207-18. doi: 10.1111/bjh.13156. Epub 2014 Oct 14. Br J Haematol. 2015. PMID: 25312307 Free article. 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.
Heterogeneity among patients with tumor necrosis factor receptor-associated periodic syndrome phenotypes.
Aganna E, Hammond L, Hawkins PN, Aldea A, McKee SA, van Amstel HK, Mischung C, Kusuhara K, Saulsbury FT, Lachmann HJ, Bybee A, McDermott EM, La Regina M, Arostegui JI, Campistol JM, Worthington S, High KP, Molloy MG, Baker N, Bidwell JL, Castañer JL, Whiteford ML, Janssens-Korpola PL, Manna R, Powell RJ, Woo P, Solis P, Minden K, Frenkel J, Yagüe J, Mirakian RM, Hitman GA, McDermott MF. Aganna E, et al. Among authors: lachmann hj. Arthritis Rheum. 2003 Sep;48(9):2632-44. doi: 10.1002/art.11215. Arthritis Rheum. 2003. PMID: 13130484 Free article.
250 results