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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: booth dr, booth se. N Engl J Med. 2002 Jun 6;346(23):1786-91. doi: 10.1056/NEJMoa013354. N Engl J Med. 2002. PMID: 12050338 Free article.
Human lysozyme gene mutations cause hereditary systemic amyloidosis.
Pepys MB, Hawkins PN, Booth DR, Vigushin DM, Tennent GA, Soutar AK, Totty N, Nguyen O, Blake CC, Terry CJ, et al. Pepys MB, et al. Among authors: booth dr. Nature. 1993 Apr 8;362(6420):553-7. doi: 10.1038/362553a0. Nature. 1993. PMID: 8464497
Molecular mechanisms of fibrillogenesis and the protective role of amyloid P component: two possible avenues for therapy.
Pepys MB, Tennent GA, Booth DR, Bellotti V, Lovat LB, Tan SY, Persey MR, Hutchinson WL, Booth SE, Madhoo S, Soutar AK, Hawkins PN, Van Zyl-Smit R, Campistol JM, Fraser PE, Radford SE, Robinson CV, Sunde M, Serpell LC, Blake CC. Pepys MB, et al. Among authors: booth dr, booth se. Ciba Found Symp. 1996;199:73-81; discussion 81-9. doi: 10.1002/9780470514924.ch6. Ciba Found Symp. 1996. PMID: 8915605
187 results