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MHC typing in variant Creutzfeldt-Jakob disease.
Pepys MB, Bybee A, Booth DR, Bishop MT, Will RG, Little AM, Prokupek B, Madrigal JA. Pepys MB, et al. Among authors: bybee a. Lancet. 2003 Feb 8;361(9356):487-9. doi: 10.1016/S0140-6736(03)12455-5. Lancet. 2003. PMID: 12583949
Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis.
Lachmann HJ, Booth DR, Booth SE, Bybee A, Gilbertson JA, Gillmore JD, Pepys MB, Hawkins PN. Lachmann HJ, et al. Among authors: bybee a. N Engl J Med. 2002 Jun 6;346(23):1786-91. doi: 10.1056/NEJMoa013354. N Engl J Med. 2002. PMID: 12050338 Free article.
Organ transplantation in hereditary apolipoprotein AI amyloidosis.
Gillmore JD, Stangou AJ, Lachmann HJ, Goodman HJ, Wechalekar AD, Acheson J, Tennent GA, Bybee A, Gilbertson J, Rowczenio D, O'Grady J, Heaton ND, Pepys MB, Hawkins PN. Gillmore JD, et al. Among authors: bybee a. Am J Transplant. 2006 Oct;6(10):2342-7. doi: 10.1111/j.1600-6143.2006.01507.x. Epub 2006 Aug 21. Am J Transplant. 2006. PMID: 16925563 Free article.
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: bybee a. Arthritis Rheum. 2002 Sep;46(9):2445-52. doi: 10.1002/art.10509. Arthritis Rheum. 2002. PMID: 12355493 Free article.
36 results