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The experience of hereditary apolipoprotein A-I amyloidosis at the UK National Amyloidosis Centre.
Cohen OC, Blakeney IJ, Law S, Ravichandran S, Gilbertson J, Rowczenio D, Mahmood S, Sachchithanantham S, Wisniowski B, Lachmann HJ, Whelan CJ, Martinez-Naharro A, Fontana M, Hawkins PN, Gillmore JD, Wechalekar AD. Cohen OC, et al. Among authors: hawkins pn. Amyloid. 2022 Dec;29(4):237-244. doi: 10.1080/13506129.2022.2070741. Epub 2022 May 3. Amyloid. 2022. PMID: 35502644 Free article.
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: hawkins pn. N Engl J Med. 2002 Jun 6;346(23):1786-91. doi: 10.1056/NEJMoa013354. N Engl J Med. 2002. PMID: 12050338 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: hawkins pn. Arthritis Rheum. 2002 Sep;46(9):2445-52. doi: 10.1002/art.10509. Arthritis Rheum. 2002. PMID: 12355493 Free article.
Novel pharmacological strategies in amyloidosis.
Lachmann HJ, Hawkins PN. Lachmann HJ, et al. Among authors: hawkins pn. Nephron Clin Pract. 2003;94(4):c85-8. doi: 10.1159/000072490. Nephron Clin Pract. 2003. PMID: 12972717 Review.
434 results