Identification of novel FLT‐3 Asp835 mutations in adult acute myeloid leukaemia von Abu‐Duhier, F. M., Goodeve, A. C., Wilson, G. A., Care, R. S., Peake, I. R., Reilly, J. T.

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FLT3 internal tandem duplication mutations in adult acute myeloid leukaemia define a high-risk group von ABU-DUHIER, F. M, GOODEVE, A. C, WILSON, G. A, GARI, M. A, PEAKE, I. R, REES, D. C, VANDENBERGHE, E. A, WINSHIP, P. R, REILLY, J. T

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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... von 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

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Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor von 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.

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Management of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization von Pasi, K. J., Collins, P. W., Keeling, D. M., Brown, S. A., Cumming, A. M., Dolan, G. C., Hay, C. R. M., Hill, F. G. H., Laffan, M., Peake, I. R.

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The diagnosis of von Willebrand disease: a guideline from the UK Haemophilia Centre Doctors' Organization von Laffan, M., Brown, S. A., Collins, P. W., Cumming, A. M., Hill, F. G. H., Keeling, D., Peake, I. R., Pasi, K. J.

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Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S von Makris, Michael, Leach, Michael, Beauchamp, Nick J., Daly, Martina E., Cooper, Peter C., Hampton, Kingsley K., Bayliss, Pauline, Peake, Ian R., Miller, George J., Preston, F. Eric

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Genetic testing for von Willebrand disease: the case for von 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 von 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

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In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion von Cartwright, A., Peake, I. R., Goodeve, A. C., Hampshire, D. J.

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Genomic structure of human FLT3: implications for mutational analysis von Abu‐Duhier, F. M., Goodeve, A. C., Wilson, G. A., Care, R. S., Peake, I. R., Reilly, J. T.

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A framework for genetic service provision for haemophilia and other inherited bleeding disorders von Ludlam, C. A., Pasi, K. J., Bolton-Maggs, P., Collins, P. W., Cumming, A. M., Dolan, G., Fryer, A., Harrington, C., Hill, F. G. H., Peake, I. R., Perry, D. J., Skirton, H., Smith, M.

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Major Structural Defects in the Antithrombin Gene in Four Families with Type I Antithrombin Deficiency Partial/complete Deletions and Rearrangement of the Antithrombin Gene von BEAUCHAMP, N. J, MAKRIS, M, PRESTON, F. E, PEAKE, I. R, DALY, M. E

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A rapid method for haemophilia B mutation detection using conformation sensitive gel electrophoresis von Hinks, J. L., Winship, P. R., Makris, M., Preston, F. E., Peake, I. R., Goodeve, A. C.

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Are aberrant BCR-ABL transcripts more common than previously thought? von WILSON, G. A, VANDENBERGHE, E. A, POLLITT, R. C, REES, D. C, GOODEVE, A. C, PEAKE, I. R, REILLY, J. T

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A Standard Nomenclature for von Willebrand Factor Gene Mutations and Polymorphisms von Goodeve, A. C., Eikenboom, J. C. J., Ginsburg, D., Hilbert, L., Mazurier, C., Peake, I. R., Sadler, J. E., Rodeghiero, F.

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Two novel type 2N von Willebrand disease–causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor von Allen, Simon, Abuzenadah, Adel M., Blagg, Joanna L., Hinks, Joanna, Nesbitt, I. Mandy, Goodeve, Anne C., Gursel, Turkiz, Ingerslev, Jørgen, Peake, Ian R., Daly, Martina E.

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Mutations in PTPN11 are uncommon in adult myelodysplastic syndromes and acute myeloid leukaemia von Johan, M. F., Bowen, D. T., Frew, M. E., Goodeve, A. C., Wilson, G. A., Peake, I. R., Reilly, J. T.

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Influence of the −675 4G/5G dimorphism of the plasminogen activator inhibitor 1 promoter on thrombotic risk in patients with factor V Leiden von Visanji, J. M., Seargent, J., Tahri, D., Croft, S. A., Makris, M., Preston, F. E., Peake, I. R., Daly, M. E.

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Factor VIII gene rearrangements in patients with severe haemophilia A von Goodeve, A.C., Preston, F.E., Peake, I.R.

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