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Heart (British Cardiac Society)|August 24, 1999
Hereditary cardiac amyloidosis associated with the transthyretin Ile122 mutation in a white manJ D Gillmore, D R Booth, M B Pepys, et al.Circulation|February 15, 1995
A novel variant of transthyretin, 59Thr-->Lys, associated with autosomal dominant cardiac amyloidosis in an Italian familyD R Booth, S Y Tan, P N Hawkins, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 27, 1999
Hereditary renal amyloidosis associated with variant lysozyme in a large English familyJ D Gillmore, D R Booth, S Madhoo, et al.QJM : Monthly Journal of the Association of Physicians|February 20, 1999
Pyrin/marenostrin mutations in familial Mediterranean feverD R Booth, J D Gillmore, S E Booth, et al.Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 26, 1999
SAA1 alleles as risk factors in reactive systemic AA amyloidosisD R Booth, S E Booth, J D Gillmore, et al.QJM : Monthly Journal of the Association of Physicians|October 6, 2001
Prevalence and significance of the familial Mediterranean fever gene mutation encoding pyrin Q148D R Booth, H J Lachmann, J D Gillmore, et al.Arthritis and Rheumatism|October 3, 2000
An autosomal dominant periodic fever associated with AA amyloidosis in a north Indian family maps to distal chromosome 1qM F McDermott, E Aganna, G A Hitman, et al.QJM : Monthly Journal of the Association of Physicians|May 29, 2000
Curative hepatorenal transplantation in systemic amyloidosis caused by the Glu526Val fibrinogen alpha-chain variant in an English familyJ D Gillmore, D R Booth, M Rela, et al.Pageof 16