Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D R Booth

Showing results (21-30 of 52) with videos related to

Pageof 6
Sort By:
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.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 1, 2007
An investigation of polymorphisms in the 4q1 3.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in AustraliansM J Bugeja, D R Booth, B H Bennetts, 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.
Human Mutation|November 3, 2000
Transthyretin Ile84Thr is associated with familial amyloid polyneuropathyD R Booth, A Stangou, R S Williams, et al.
Oncogene|September 20, 2005
The elusive multiple self-healing squamous epithelioma (MSSE) gene: further mapping, analysis of candidates, and loss of heterozygosityS Bose, L J Morgan, D R Booth, et al.
Internal Medicine Journal|January 27, 2012
Vitreal deposits in Val71Ala transthyretin amyloidosisD Suan, D R Booth, I H Kennedy, 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.
Genes and Immunity|October 12, 2007
Haplotypes of the interleukin 7 receptor alpha gene are correlated with altered expression in whole blood cells in multiple sclerosisF C McKay, L I Swain, S D Schibeci, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
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.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 1, 2007
An investigation of polymorphisms in the 4q1 3.3-21.1 CXC chemokine gene cluster for association with multiple sclerosis in AustraliansM J Bugeja, D R Booth, B H Bennetts, 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.
Human Mutation|November 3, 2000
Transthyretin Ile84Thr is associated with familial amyloid polyneuropathyD R Booth, A Stangou, R S Williams, et al.
Oncogene|September 20, 2005
The elusive multiple self-healing squamous epithelioma (MSSE) gene: further mapping, analysis of candidates, and loss of heterozygosityS Bose, L J Morgan, D R Booth, et al.
Internal Medicine Journal|January 27, 2012
Vitreal deposits in Val71Ala transthyretin amyloidosisD Suan, D R Booth, I H Kennedy, 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.
Genes and Immunity|October 12, 2007
Haplotypes of the interleukin 7 receptor alpha gene are correlated with altered expression in whole blood cells in multiple sclerosisF C McKay, L I Swain, S D Schibeci, et al.
Pageof 6