N. Totty

Human lysozyme gene mutations cause hereditary systemic amyloidosis

D. Booth, C. Blake, M. Pepys, 1993, Nature.

A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosis.

D. Booth, D. Vigushin, G. Tennent, 1995, QJM : monthly journal of the Association of Physicians.

Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.

P. Hawkins, D. Vigushin, G. Tennent, 1992, Proceedings of the National Academy of Sciences of the United States of America.

AL kappa amyloid in a solitary extradural lymphoma.

M. Pepys, P. Hawkins, D. Vigushin, 1994, Journal of neurology, neurosurgery, and psychiatry.

ALK amyloid in a solitary extradural lymphoma

D. Vigushin, N. Totty, J. Hsuan, 2022 .

Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene.

D. Booth, M. Pepys, P. Hawkins, 1996, The Journal of clinical investigation.

Identification of the circulating amyloid precursor and other gelsolin metabolites in patients with G654A mutation in the gelsolin gene (Finnish familial amyloidosis): pathogenetic and diagnostic implications.

K. Sletten, N. Totty, C. Maury, 1997, Laboratory investigation; a journal of technical methods and pathology.