Conference report: International Haemovigilance Seminar and the SHOT Annual Symposium, 10–12 July 2018 von Bolton‐Maggs, P.H.B.

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A common ancestral mutation (C128X) occurring in 11 non‐Jewish families from the UK with factor XI deficiency von Bolton‐Maggs, P. H. B., Peretz, H., Butler, R., Mountford, R., Keeney, S., Zacharski, L., Zivelin, A., Seligsohn, U.

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Blood transfusion: risks and benefits von Bolton-Maggs, P.H.B, Murphy, M.F

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Thrombogenic potential of factor XI concentrate von Bolton-Maggs, P.H.B, Colvin, B.T, Satchi, G, Lee, C.A, Lucas, G.S

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Idiopathic multifocal intracardiac and pulmonary thrombosis: successful treatment with rTPA von Holzer, R, Peart, I, Ciotti, G, Bolton-Maggs, P H B

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Diffuse angioma-like changes associated with chronic DIC von BOLTON-MAGGS, P.H.B., RUSTIN, M.H.A.

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The rarer inherited coagulation disorders: A review von Bolton-Maggs, P.H.B., Hill, F.G.H.

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Investigation of the neutropenic child von Bolton-Maggs, P.H.B

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