S E Booth

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

Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis.

Anne K. Soutar, Philip N. Hawkins, David M. Vigushin et al. · Proceedings of the National Academy of Sciences · 1992 · 144 citations

Life Sciences, Genetics, Molecular Genetics +14

Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis

Molly S. Brett, M.R. Persey, Mary M. Reilly et al. · Brain · 1999 · 113 citations

Medicine, Neurology, Neuroscience +17

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

David R. Booth, Shouyong Tan, S E Booth et al. · Journal of Clinical Investigation · 1996 · 106 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Binding of pentraxins to different nuclear structures: C-reactive protein binds to small nuclear ribonucleoprotein particles, serum amyloid P component binds to chromatin and nucleoli

Mark B. Pepys, S E Booth, Glenys A. Tennent et al. · Clinical & Experimental Immunology · 1994 · 103 citations

Life Sciences, Biochemistry, Cell Biology +12