David R. Booth

Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis

David R. Booth, Margaret Sunde, Vittorio Bellotti et al. · Nature · 1997 · 1K citations

Human Lysozyme Variants, Alzheimer's Disease, Protein Assembly +7

Misdiagnosis of Hereditary Amyloidosis as AL (Primary) Amyloidosis

Helen J. Lachmann, David R. Booth, Susanne E. Booth et al. · New England Journal of Medicine · 2002 · 683 citations · Full text

Human lysozyme gene mutations cause hereditary systemic amyloidosis

Mark B. Pepys, Philip N. Hawkins, David R. Booth et al. · Nature · 1993 · 655 citations

Alzheimer's Disease, Mendelian Disorder, Genetic Disorder +6

Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations

Helen J. Lachmann, Bülent Şengül, Tuğba Yavuzşen et al. · Lara D. Veeken · 2006 · 368 citations · Full text

Association of mutations in the <i>NALP3/CIAS1/PYPAF1</i> gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis

Ebun Aganna, Fabio Martinon, Philip N. Hawkins et al. · Arthritis & Rheumatism · 2002 · 362 citations