Torthaí cuardaigh - Angie Tuttle
- 1 - 5 toradh as 5 á dtaispeáint
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1
Generation and optimization of the self‐administered bleeding assessment tool and its validation as a screening test for von Willebrand disease de réir M. Deforest, Julie Grabell, Sébastien Albert, Jun Young, Angie Tuttle, Wilma M. Hopman, P. D. James
Foilsithe / Cruthaithe 2015Artigo -
2
The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles de réir Mackenzie Bowman, Angie Tuttle, Colleen Notley, C. Brown, Shawn Tinlin, M. Deforest, Jayne Leggo, VS. Blanchette, David Lillicrap, Paula James
Foilsithe / Cruthaithe 2013Artigo -
3
A MicroRNA-regulated and GP64-pseudotyped Lentiviral Vector Mediates Stable Expression of FVIII in a Murine Model of Hemophilia A de réir Hideto Matsui, Carol Hegadorn, Margareth C. Ozelo, Erin Burnett, Angie Tuttle, Andrea Labelle, Paul B. McCray, Luigi Naldini, Brian D. Brown, Christine Hough, David Lillicrap
Foilsithe / Cruthaithe 2011Artigo -
4
Normal range of bleeding scores for the ISTH‐BAT: adult and pediatric data from the merging project de réir Malak Elbatarny, Shamim Mollah, Julie Grabell, Steven S. Bae, M. Deforest, Angie Tuttle, Wilma M. Hopman, Dewi Clark, Andreas C. Mauer, Mackenzie Bowman, James Riddel, Pamela A. Christopherson, Robert R. Montgomery, Margaret L. Rand, Barry S. Coller, Paula James
Foilsithe / Cruthaithe 2014Artigo -
5
The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study de réir Paula D. James, Colleen Notley, Carol Hegadorn, Jayne Leggo, Angie Tuttle, Shawn Tinlin, Christine Brown, C. Webb Andrews, Andrea Labelle, Yvette Chirinian, Lee A. O’Brien, Maha Othman, Georges E. Rivard, D. RAPSON, Christine Hough, David Lillicrap
Foilsithe / Cruthaithe 2006Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Gene
Immunology
Medicine
Platelet
Von Willebrand disease
Von Willebrand factor
Biochemistry
Genetics
Genotype
Internal medicine
Missense mutation
Mutation
Nonsense mutation
Allele
Antibody
Cancer research
Compound heterozygosity
Context (archaeology)
Factor IX
Frameshift mutation
Gene delivery
Genetic enhancement
Gerontology
Immune system
MEDLINE
Paleontology
Pediatrics
Physics
Point mutation