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Prevalence, characteristics and outcomes of older patients with hereditary versus wild-type transthyretin amyloid cardiomyopathy.
Porcari A, Razvi Y, Masi A, Patel R, Ioannou A, Rauf MU, Hutt DF, Rowczenio D, Gilbertson J, Martinez-Naharro A, Venneri L, Whelan C, Lachmann H, Wechalekar A, Quarta CC, Merlo M, Sinagra G, Hawkins PN, Fontana M, Gillmore JD. Porcari A, et al. Among authors: hawkins pn. Eur J Heart Fail. 2023 Apr;25(4):515-524. doi: 10.1002/ejhf.2776. Epub 2023 Jan 30. Eur J Heart Fail. 2023. PMID: 36644836 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.
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.
Systemic amyloidosis.
Lachmann HJ, Hawkins PN. Lachmann HJ, et al. Among authors: hawkins pn. Curr Opin Pharmacol. 2006 Apr;6(2):214-20. doi: 10.1016/j.coph.2005.10.005. Epub 2006 Feb 17. Curr Opin Pharmacol. 2006. PMID: 16483845 Review.
425 results