Early discharge of patients with pulmonary embolism: a two-phase observational study von Davies, C. W. H, Wimperis, J, Green, E. S, Pendry, K, Killen, J, Mehdi, I, Tiplady, C, Kesteven, P, Rose, P, Oldfield, W

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Incidence of liver disease in people with HFE mutations von Willis, G, Wimperis, J Z, Lonsdale, R, Fellows, I W, Watson, M A, Skipper, L M, Jennings, B A

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Resolution of chronic severe refractory thrombocytopenia after treatment of hypothyroidism von Bowles, K M, Turner, G E, Wimperis, J Z

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HFE mutations in an inflammatory arthritis population von Willis, G., Scott, D. G. I., Jennings, B. A., Smith, K., Bukhari, M., Wimperis, J. Z.

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Haemochromatosis gene C282Y homozygotes in an elderly male population von Willis, Gavin, Wimperis, Jennie Z, Smith, Katy C, Fellows, Ian W, Jennings, Barbara A

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Guidelines on obtaining consent for systemic anti-cancer therapy in adults von Treleaven, J., Gadd, E., Cullis, J., Favre, J., McLeod, A., Meller, S., Milligan, D., Neilson, R., Quinn, B., Webb, A., Wimperis, J.

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UK patients with deep‐vein thrombosis can be safely treated as out‐patients von O'Shaughnessy, D., Miles, J., Wimperis, J.

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Facilities for the treatment of adults with haematological malignancies - 'Levels of Care': BCSH Haemato-Oncology Task Force 2009 von Matthey, F., Parker, A., Rule, S. A. J., Wimperis, J. Z., Ardeshna, K. M., Bird, J. M., Cullis, J., Lyttelton, M. P. A., McMillan, A., Jackson, G. H.

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Haemochromatosis gene mutation in hepatocellular cancer von Willis, G, Wimperis, JZ, Lonsdale, R, Jennings, BA

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Laparoscopic splenectomy: single‐centre experience of a district general hospital von BERNARD, T, RHODES, M, TURNER, G. E, WIMPERIS, J. Z, DEANE, A. M

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Serum prohepcidin concentration: no association with iron absorption in healthy men; and no relationship with iron status in men carrying HFE mutations, hereditary haemochromatosis... von Roe, Mark A., Spinks, Caroline, Heath, Anne-Louise M., Harvey, Linda J., Foxall, Rob, Wimperis, Jennie, Wolf , Christian, Fairweather-Tait, Susan J.

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ERWIN: an E-region wind interferometer von Gault, W A, Brown, S, Moise, A, Liang, D, Sellar, G, Shepherd, G G, Wimperis, J

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Linkage analysis for major histocompatibility complex–related genetic susceptibility in familial chronic lymphocytic leukemia von Bevan, Stephen, Catovsky, Daniel, Matutes, Estella, Antunovic, Petar, Auger, Martin J., Ben-Bassat, Isaac, Bell, Andrew, Berrebi, Alain, Gaminara, Elizabeth J., Júnior, Maria E., Mauro, Francesca R., Quabeck, Klas, Rassam, Saad M.B., Reid, Cecil, Ribeiro, Isabel, Stark, Pinhas, van Dongen, Jacques J.M., Wimperis, Jennifer, Wright, Susan, Marossy, Andrea, Yuille, Martin R., Houlston, Richard S.

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Bedside filtration of blood products in the prevention of HLA alloimmunization. A prospective randomized study von WILLIAMSON, L. M, WIMPERIS, J. Z, WILLIAMSON, P, COPPLESTONE, J. A, GOOI, H. C, MORGENSTERN, G. R, NORFOLK, D. R

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Unusually Severe Heterozygous β-Thalassemia: Evidence for an Interacting Gene Affecting Globin Translation von Ho, P. Joy, Hall, Georgina W., Watt, Suzanne, West, Nicholas C., Wimperis, Jennifer W., Wood, William G., Thein, Swee Lay

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Fludarabine treatment and transfusion-associated graft-versus-host disease von Williamson, Lorna M, Wimperis, Jennie Z, Wood, Marion E, Woodcock, Barrie

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Linkage analysis for ATM in familial B cell chronic lymphocytic leukaemia von BEVAN, S, CATOVSKY, D, RIBEIRO, I, MAURO, F. R, STARK, P, SYKES, H, VAN DONGEN, J, WIMPERIS, J, WRIGHT, S, YUILLE, M. R, HOULSTON, R. S, MAROSSY, A, MATUTES, E, POPAT, S, ANTONOVIC, P, BELL, A, BERREBI, A, GAMINARA, E. J, QUABECK, K

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Robust monolithic ultraviolet interferometer for the SHIMMER instrument on STPSat-1 von Harlander, John M, Roesler, Fred L, Englert, Christoph R, Cardon, Joel G, Conway, Robert R, Brown, Charles M, Wimperis, Jeff

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Expression of Human Interleukin-3 (multi-CSF) Is Restricted to Human Lymphocytes and T-Cell Tumor Lines von Niemeyer, Charlotte M, Sieff, Colin A, Mathey-Prevot, Bernard, Wimperis, Jennifer Z, Bierer, Barbara E, Clark, Steven C, Nathan, David G

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A High Prevalence of HLA-H 845A Mutations in Hemochromatosis Patients and the Normal Population in Eastern England von Willis, Gavin, Jennings, Barbara A., Goodman, Emma, Fellows, Ian W., Wimperis, Jennie Z.

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