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	21.	SAA1 alleles as risk factors in reactive systemic AA amyloidosis. [electronic resource] by Booth, D R Booth, S E Gillmore, J D Hawkins, P N Pepys, M B Producer: 19990428 In: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Prevalence and significance of the familial Mediterranean fever gene mutation encoding pyrin Q148. [electronic resource] by Booth, D R Lachmann, H J Gillmore, J D Booth, S E Hawkins, P N Producer: 20011205 In: QJM : monthly journal of the Association of Physicians vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Pyrin/marenostrin mutations in familial Mediterranean fever. [electronic resource] by Booth, D R Gillmore, J D Booth, S E Pepys, M B Hawkins, P N Producer: 19990308 In: QJM : monthly journal of the Association of Physicians vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	An investigation of polymorphisms in the 4q1 3.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in Australians. [electronic resource] by Bugeja, M J Booth, D R Bennetts, B H Heard, R N S Stewart, G J Producer: 20070228 In: Multiple sclerosis (Houndmills, Basingstoke, England) vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	An autosomal dominant periodic fever associated with AA amyloidosis in a north Indian family maps to distal chromosome 1q. [electronic resource] by McDermott, M F Aganna, E Hitman, G A Ogunkolade, B W Booth, D R Hawkins, P N Producer: 20001019 In: Arthritis and rheumatism vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Transthyretin Ile84Thr is associated with familial amyloid polyneuropathy. [electronic resource] by Booth, D R Stangou, A Williams, R S Gillmore, J D Tennent, G A Hawkins, P N Producer: 20001121 In: Human mutation vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	The elusive multiple self-healing squamous epithelioma (MSSE) gene: further mapping, analysis of candidates, and loss of heterozygosity. [electronic resource] by Bose, S Morgan, L J Booth, D R Goudie, D R Ferguson-Smith, M A Richards, F M Producer: 20060403 In: Oncogene vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Vitreal deposits in Val71Ala transthyretin amyloidosis. [electronic resource] by Suan, D Booth, D R Kennedy, I H Downie, J Earls, P Gottlieb, D Stewart, G J Lin, M-W Producer: 20120601 In: Internal medicine journal vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Curative hepatorenal transplantation in systemic amyloidosis caused by the Glu526Val fibrinogen alpha-chain variant in an English family. [electronic resource] by Gillmore, J D Booth, D R Rela, M Heaton, N D Rahman, V Stangou, A J Pepys, M B Hawkins, P N Producer: 20000802 In: QJM : monthly journal of the Association of Physicians vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26. [electronic resource] by Vigushin, D M Gough, J Allan, D Alguacil, A Penner, B Pettigrew, N M Quinonez, G Bernstein, K Booth, S E Booth, D R Producer: 19940712 In: The Quarterly journal of medicine vol. 87 Availability: No items available. Save to lists Add to cart (remove)
	31.	Haplotypes of the interleukin 7 receptor alpha gene are correlated with altered expression in whole blood cells in multiple sclerosis. [electronic resource] by McKay, F C Swain, L I Schibeci, S D Rubio, J P Kilpatrick, T J Heard, R N Stewart, G J Booth, D R Producer: 20080327 In: Genes and immunity vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy. [electronic resource] by Reilly, M M Adams, D Booth, D R Davis, M B Said, G Laubriat-Bianchin, M Pepys, M B Thomas, P K Harding, A E Producer: 19950929 In: Brain : a journal of neurology vol. 118 ( Pt 4) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis. [electronic resource] by Brett, M Persey, M R Reilly, M M Revesz, T Booth, D R Booth, S E Hawkins, P N Pepys, M B Morgan-Hughes, J A Producer: 19990318 In: Brain : a journal of neurology vol. 122 ( Pt 2) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	The genetic basis of autosomal dominant familial Mediterranean fever. [electronic resource] by Booth, D R Gillmore, J D Lachmann, H J Booth, S E Bybee, A Soytürk, M Akar, S Pepys, M B Tunca, M Hawkins, P N Producer: 20001030 In: QJM : monthly journal of the Association of Physicians vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Gene expression and genotyping studies implicate the interleukin 7 receptor in the pathogenesis of primary progressive multiple sclerosis. [electronic resource] by Booth, D R Arthur, A T Teutsch, S M Bye, C Rubio, J Armati, P J Pollard, J D Heard, R N S Stewart, G J Producer: 20060327 In: Journal of molecular medicine (Berlin, Germany) vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-I. [electronic resource] by Persey, M R Booth, D R Booth, S E van Zyl-Smit, R Adams, B K Fattaar, A B Tennent, G A Hawkins, P N Pepys, M B Producer: 19980319 In: Kidney international vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26Arg. [electronic resource] by Gillmore, J D Stangou, A J Tennent, G A Booth, D R O'Grady, J Rela, M Heaton, N D Wall, C A Keogh, J A Hawkins, P N Producer: 20010531 In: Transplantation vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations. [electronic resource] by Lachmann, H J Sengül, B Yavuzşen, T U Booth, D R Booth, S E Bybee, A Gallimore, J R Soytürk, M Akar, S Tunca, M Hawkins, P N Producer: 20060804 In: Rheumatology (Oxford, England) vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosis. [electronic resource] by Booth, D R Tan, S Y Booth, S E Hsuan, J J Totty, N F Nguyen, O Hutton, T Vigushin, D M Tennent, G A Hutchinson, W L Producer: 19960111 In: QJM : monthly journal of the Association of Physicians vol. 88 Availability: No items available. Save to lists Add to cart (remove)
	40.	Human lysozyme gene mutations cause hereditary systemic amyloidosis. [electronic resource] by Pepys, M B Hawkins, P N Booth, D R Vigushin, D M Tennent, G A Soutar, A K Totty, N Nguyen, O Blake, C C Terry, C J Producer: 19930503 In: Nature vol. 362 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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