Zobrazeno 1 - 10
of 113
pro vyhledávání: '"C.R Rizza"'
Publikováno v:
Human molecular genetics. 2(1)
Haemophilia A is a mutationally heterogeneous disease caused by defects in the large and complex factor VIII gene. Recent studies examining the putative promoter, all exons and most intron/exon boundaries have failed to detect mutations in half the p
Autor:
C.R. Rizza
Publikováno v:
Current Orthopaedics. 1:299-309
Autor:
G.I.C. Ingram, C.R. Rizza
Publikováno v:
Acta Haematologica. 55:48-52
A woman with symptoms of prolonged post-traumatic bleeding was found to have a severe defect of factor XI, and was thought to be homozygously affected. Both her parents, who were first cousins, and all her three children, though asymptomatic, showed
Autor:
C.R. Rizza
Publikováno v:
Clinics in Haematology. 5:113-133
Autor:
K.H Choo, C.R Rizza, P.R Winship, Francesco Giannelli, George G. Brownlee, N Ferrari, D. S. Anson
Publikováno v:
The Lancet. 323:239-241
DNA from 33 healthy White subjects was analysed with a 2·5 kilobase subgenomic DNA probe derived from the gene for coagulation factor IX, containing the exon "d" region of that gene. Intragenic Taq I restriction-fragment length polymorphism was reve
Autor:
D.E.G. Austen, C.R. Rizza
Publikováno v:
Lancet (London, England). 2(8242)
Publikováno v:
Thrombosis and Haemostasis.
In assays of factor VIII antibody the patient’s antibody - containing plasma is allowed to react with factor VIII for a given length of time, the residual factor VIII assayed and the level of antibody calculated in arbitrarily defined units. The se
Publikováno v:
The Lancet. 315:820
Publikováno v:
The Lancet. 333:960
Autor:
C.R. Rizza, P.B.A. Kernoff
Publikováno v:
The Lancet. 302:734