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Rheumatology (Oxford, England)|January 13, 2006
Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutationsH J Lachmann, B Sengül, T U Yavuzşen, et al.Journal of Internal Medicine|June 17, 2015
Cardiac amyloidosis: where are we today?K S Patel, P N HawkinsClinical and Experimental Immunology|August 1, 1990
A primed state exists in vivo following histological regression of amyloidosisP N Hawkins, M B PepysThe International Journal of Biochemistry & Cell Biology|September 10, 2003
Amyloidosis: new strategies for treatmentG M Hirschfield, P N HawkinsNature|April 8, 1993
Human lysozyme gene mutations cause hereditary systemic amyloidosisM B Pepys, P N Hawkins, D R Booth, et al.International Journal of Oral Surgery|December 1, 1975
The early effects of segmental surgery on the human pulpL Summers, D R BoothHuman Mutation|March 1, 2000
Transthyretin Ile73Val is associated with familial amyloidotic polyneuropathy in a Bangladeshi family. Mutations in brief no. 158. OnlineD R Booth, J D Gillmore, M R Persey, et al.Nature|February 27, 1997
Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesisD R Booth, M Sunde, V Bellotti, et al.The Journal of Clinical Investigation|December 1, 1990
Metabolic studies of radioiodinated serum amyloid P component in normal subjects and patients with systemic amyloidosisP N Hawkins, R Wootton, M B PepysPageof 16