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D R Booth

Showing results (31-40 of 52) with videos related to

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The Quarterly Journal of Medicine|March 1, 1994
Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26D M Vigushin, J Gough, D Allan, et al.
Brain : a Journal of Neurology|August 1, 1995
Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathyM M Reilly, D Adams, D R Booth, et al.
QJM : Monthly Journal of the Association of Physicians|April 29, 2000
The genetic basis of autosomal dominant familial Mediterranean feverD R Booth, J D Gillmore, H J Lachmann, et al.
Brain : a Journal of Neurology|March 10, 1999
Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosisM Brett, M R Persey, M M Reilly, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 3, 2005
Gene expression and genotyping studies implicate the interleukin 7 receptor in the pathogenesis of primary progressive multiple sclerosisD R Booth, A T Arthur, S M Teutsch, et al.
Genes and Immunity|March 18, 2016
Cistromic and genetic evidence that the vitamin D receptor mediates susceptibility to latitude-dependent autoimmune diseasesD R Booth, N Ding, G P Parnell, et al.
Kidney International|February 14, 1998
Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-IM R Persey, D R Booth, S E Booth, et al.
Transplantation|May 15, 2001
Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26ArgJ D Gillmore, A J Stangou, G A Tennent, et al.
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.
QJM : Monthly Journal of the Association of Physicians|October 1, 1995
A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosisD R Booth, S Y Tan, S E Booth, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
The Quarterly Journal of Medicine|March 1, 1994
Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26D M Vigushin, J Gough, D Allan, et al.
Brain : a Journal of Neurology|August 1, 1995
Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathyM M Reilly, D Adams, D R Booth, et al.
QJM : Monthly Journal of the Association of Physicians|April 29, 2000
The genetic basis of autosomal dominant familial Mediterranean feverD R Booth, J D Gillmore, H J Lachmann, et al.
Brain : a Journal of Neurology|March 10, 1999
Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosisM Brett, M R Persey, M M Reilly, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 3, 2005
Gene expression and genotyping studies implicate the interleukin 7 receptor in the pathogenesis of primary progressive multiple sclerosisD R Booth, A T Arthur, S M Teutsch, et al.
Genes and Immunity|March 18, 2016
Cistromic and genetic evidence that the vitamin D receptor mediates susceptibility to latitude-dependent autoimmune diseasesD R Booth, N Ding, G P Parnell, et al.
Kidney International|February 14, 1998
Hereditary nephropathic systemic amyloidosis caused by a novel variant apolipoprotein A-IM R Persey, D R Booth, S E Booth, et al.
Transplantation|May 15, 2001
Clinical and biochemical outcome of hepatorenal transplantation for hereditary systemic amyloidosis associated with apolipoprotein AI Gly26ArgJ D Gillmore, A J Stangou, G A Tennent, et al.
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.
QJM : Monthly Journal of the Association of Physicians|October 1, 1995
A new apolipoprotein Al variant, Trp50Arg, causes hereditary amyloidosisD R Booth, S Y Tan, S E Booth, et al.
Pageof 6