A Bybee

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 · 687 citations · Full text

Life Sciences, Genetics, Pathology +14

Serum amyloid P component controls chromatin degradation and prevents antinuclear autoimmunity

Maria C. M. Bickerstaff, Marina Botto, W. L. Hutchinson et al. · Nature Medicine · 1999 · 490 citations

Life Sciences, Immunology, Molecular Biology +10

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 · 374 citations · Full text

Veterinary Medicine, Clinical Sciences, Molecular Genetics +9

Heterogeneity among patients with tumor necrosis factor receptor–associated periodic syndrome phenotypes

Ebun Aganna, L Hammond, Philip N. Hawkins et al. · Arthritis & Rheumatism · 2003 · 194 citations

Medicine, Immunology, Molecular Genetics +17

Phenotype, Genotype, and Sustained Response to Anakinra in 22 Patients With Autoinflammatory Disease Associated With CIAS-1/NALP3 Mutations

Kieron Leslie, Helen J. Lachmann, Elizabeth Bruning et al. · Archives of Dermatology · 2006 · 188 citations

Medicine, Dermatology, Immunology +17