Search Results - "Peake, I.R."

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor by SADLER, J. E., BUDDE, U., EIKENBOOM, J. C. J., FAVALORO, E. J., HILL, F. G. H., HOLMBERG, L., INGERSLEV, J., LEE, C. A., LILLICRAP, D., MANNUCCI, P. M., MAZURIER, C., MEYER, D., NICHOLS, W. L., NISHINO, M., PEAKE, I. R., RODEGHIERO, F., SCHNEPPENHEIM, R., RUGGERI, Z. M., SRIVASTAVA, A., MONTGOMERY, R. R., FEDERICI, A. B.

“…von Willebrand disease (VWD) is a bleeding disorder caused by inherited defects in the concentration, structure, or function of von Willebrand factor (VWF)…”
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Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD by Castaman, G, Tosetto, A, Cappelletti, A, Goodeve, A, Federici, A.B, Batlle, J, Meyer, D, Goudemand, J, Eikenboom, J.C.J, Schneppenheim, R, Budde, U, Ingerslev, J, Lethagen, S, Hill, F, Peake, I.R, Rodeghiero, F

“…Abstract Background Accurate measurement of von Willebrand factor (VWF) is a critical requirement for the diagnosis of von Willebrand disease (VWD). Aim of the…”
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Genetic testing for von Willebrand disease: the case for by PEAKE, I. R., GOODEVE, A. C.

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THE ISTH SSC VON WILLEBRAND FACTOR (VWF) ONLINE DATABASE by Hampshire, D.J., James, P.D., Lillicrap, D., Peake, I.R., Goodeve, A.C.

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Antithrombins Wibble and Wobble (T85M/K): Archetypal Conformational Diseases With In Vivo Latent-Transition, Thrombosis, and Heparin Activation by Beauchamp, N.J., Pike, R.N., Daly, M., Butler, L., Makris, M., Dafforn, T.R., Zhou, A., Fitton, H.L., Preston, F.E., Peake, I.R., Carrell, R.W.

“…The inherent variability of conformational diseases is demonstrated by two families with different mutations of the same conserved aminoacid in antithrombin…”
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Antithrombins Wibble and Wobble (T85M/K) : Archetypal conformational diseases with in vivo latent-transition, thrombosis, and heparin activation by BEAUCHAMP, N. J, PIKE, R. N, CARRELL, R. W, DALY, M, BUTLER, L, MAKRIS, M, DAFFORN, T. R, ZHOU, A, FITTON, H. L, PRESTON, F. E, PEAKE, I. R

“…The inherent variability of conformational diseases is demonstrated by two families with different mutations of the same conserved aminoacid in antithrombin…”
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Common VWF Haplotypes in Normal African-Americans and Caucasians Recruited into the ZPMCB-VWD and Their Impact on VWF Laboratory Testing by Flood, Veronica H., Kautza, B.C., Miller, C.A., Branchford, B.R., Gill, J.C., Haberichter, S.L., Morateck, P.A., Christopherson, P.A., Perry, C.L., Friedman, K.D., Bellissimo, D.B., Abshire, T.C., Di Paola, J.A, Hoots, W.K., Leissinger, C., Lusher, J.M., Ragni, M.V., Shapiro, Ad, Lillicrap, D., Goodeve, A.C., Peake, I.R., Montgomery, R.R.

“…Von Willebrand disease (VWD) is a common bleeding disorder that has been reported to affect up to 1% of the population. Diagnostic testing for VWD relies on…”
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Family Studies and Prenatal Diagnosis in Severe von Willebrand Disease by Polymerase Chain Reaction Amplification of a Variable Number Tandem Repeat Region of the von Willebrand Factor Gene by Peake, I.R., Bowen, D., Bignell, P., Lidded, M.B., Sadler, J.E., Standen, G., Bloom, A.L.

“…We have previously demonstrated within intron 40 of the von Willebrand factor (vWF) gene a region of ATCT repeats that was shown to vary in length between two…”
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Haemophilia A: database of ncleotide substituttions, deletions, insertions and rearrangements of the factor VIII gene by Tuddenham, E.G.D., Cooper, D.N., Gitschier, J., Higuchi, M., Hoyer, L.W., Yoshioka, A., Peake, I.R., Schwaab, R., Olek, K., Kazazian, H.H., Lavergne, J.M., Giannelli, F., Antonarakis, S.E.

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Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition by Tuddenham, E.G.D., Schwaab, R., Seehafer, J., Millar, D.S., Gitschier, J., Higuchi, M., Bidichandani, S., Connor, J.M., Hoyer, L.W., Yoshioka, A., Peake, I.R., Olek, K., Kazazian, H.H., Lavergne, J.-M., Giannelli, F., Antonarakis, S.E., Cooper, D.N.

“…A large number of different mutations in the factor VIII (F8) gene have been identified as a cause of haemophilia A. This compilation lists known single…”
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Factor VIII gene rearrangements in patients with severe haemophilia A by Goodeve, A C, Preston, F E, Peake, I R

“…Sequences within intron 22 of the factor VIII (FVIII) gene have been implicated in the cause of haemophilia in almost 50% of severely affected patients. The…”
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Haemophilia: strategies for carrier detection and prenatal diagnosis by PEAKE, I. R, LILLICRAP, D. P, TUDDENHAM, E. G. D, BOULYJENKOV, V, BRIET, E, CHAN, V, GINTER, E. K, KRAUS, E. M, LJUNG, R, MANNUCCI, P. M, NICOLAIDES, K

“…In 1977 WHO published in the Bulletin a Memorandum on Methods for the Detection of Haemophilia Carriers. This was produced following a WHO/WFH (World…”
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Report of a joint WHO/WFH meeting on the control of haemophilia: carrier detection and prenatal diagnosis by Peake, I R, Lillicrap, D P, Boulyjenkov, V, Briët, E, Chan, V, Ginter, E K, Kraus, E M, Ljung, R, Mannucci, P M, Nicolaides, K

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A at ll polymorphism in von Willebrand factor gene at codon 471 by Bowen, D.J., Webb, C.E., Peake, I.R., Bloom, A.L.

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Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene, second edition by Tuddenham, E.G.D., Schwaab, R., Seehafer, J., Millar, D.S., Gitschier, J., Higuchi, M., Bidichandani, S., Connor, J.M., Hoyer, L.W., Yoshioka, A., Peake, I.R., Olek, K., Kazazian, H.H., Lavergne, J.-M., Giannelli, F., Antonarakis, S.E., Cooper, D.N.

“…A large number of different mutations in the factor VIII (F8) gene have been identified as a cause of haemophilia A. This compilation lists known single…”
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Rapid neonatal diagnosis of von Willebrand's disease by use of the polymerase chain reaction by Bignell, P, Standen, G R, Bowen, D J, Peake, I R, Bloom, A L

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AatII polymorphism in von Willebrand factor gene at codon 471 by Bowen, D J, Webb, C E, Peake, I R, Bloom, A L

“…(DBO)…”
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The relationship of HIV-1 viral sequences detected by the polymerase chain reaction in haemophilic patients to clinical and other markers of infection by Dannatt, A H, Goodwin, S J, Dasani, H, Bowen, D J, Peake, I R, Bloom, A L

“…A nested primer polymerase chain reaction (PCR) of pol gene sequences of human immunodeficiency virus-1 (HIV-1) was applied to whole blood of 31 haemophiliacs…”
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Studies on the relationship between factor VIII related antigen (VIIIRAg) and factor VIII clotting antigen (VIIICAg) by immunoelectrophoresis and autoradiography using 125I anti VIIICAg by Davies, B L, Furlong, R A, Peake, I R

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Alpha- and gamma-tocopherol in the rat: in vitro and in vivo tissue uptake and metabolism by Peake, I R, Bieri, J G

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