Inherited disorders of platelet function: selected updates von Nurden, A.T., Nurden, P.

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Diagnosis of inherited platelet function disorders: guidance from the SSC of the ISTH von Gresele, P., Harrison, P., Gachet, C., Hayward, C., Kenny, D., Mezzano, D., Mumford, A. D., Nugent, D., Nurden, A. T., Cattaneo, M.

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Professor Gustav Victor Rudolph Born (29 July 1921 – 16 April 2018) von Nurden, A. T.

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Induction of megakaryocytes to synthesize and store a releasable pool of human factor VIII von Wilcox, D. A., Shi, Q., Nurden, P., Haberichter, S. L., Rosenberg, J. B., Johnson, B. D., Nurden, A. T., Ii, G. C. White, Montgomery, R. R.

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Diagnosis of suspected inherited platelet function disorders: results of a worldwide survey von Gresele, P., Harrison, P., Bury, L., Falcinelli, E., Gachet, C., Hayward, C. P., Kenny, D., Mezzano, D., Mumford, A. D., Nugent, D., Nurden, A. T., Orsini, S., Cattaneo, M.

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Qualitative disorders of platelets and megakaryocytes von NURDEN, A. T.

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An adenine insertion in exon 6 of human GP6 generates a truncated protein associated with a bleeding disorder in four Chilean families von Matus, V., Valenzuela, G., Sáez, C. G., Hidalgo, P., Lagos, M., Aranda, E., Panes, O., Pereira, J., Pillois, X., Nurden, A. T., Mezzano, D.

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C560Rβ3 caused platelet integrin αIIbβ3 to bind fibrinogen continuously, but resulted in a severe bleeding syndrome and increased murine mortality von Fang, J., Nurden, P., North, P., Nurden, A. T., Du, L. M., Valentin, N., Wilcox, D. A.

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Glanzmann thrombasthenia: the need for epidemiological studies von NURDEN, A. T.

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An acquired inhibitor to the GPVI platelet collagen receptor in a patient with lupus nephritis von NURDEN, P., TANDON, N., TAKIZAWA, H., COUZI, L., MOREL, D., FIORE, M., PILLOIS, X., LOYAU, S., JANDROT‐PERRUS, M., NURDEN, A. T.

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Altered megakaryocytopoiesis in von Willebrand type 2B disease von NURDEN, A. T., FEDERICI, A. B., NURDEN, P.

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Mutation analysis for a patient with Glanzmann thrombasthenia who produced a landmark isoantibody to the αIIbβ3 integrin von NURDEN, A. T., KUNICKI, T., NURDEN, P., FIORE, M., MARTINS, N., HEILIG, R., PILLOIS, X.

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Does ATP act through P2X1 receptors to regulate platelet activation and thrombus formation? von NURDEN, A. T.

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Expression of platelet membrane glycoproteins and alpha‐granule proteins by a human erythroleukemia cell line (HEL) von Tabilio, A., Rosa, J.P., Testa, U., Kieffer, N., Nurden, A.T., Del Canizo, M.C., Breton‐Gorius, J., Vainchenker, W.

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Interesting variations on how a disease is defined: comparisons of von Willebrand disease and Glanzmann thrombasthenia von NURDEN, A. T.

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Polymorphisms and platelet genotyping: the shape of things to come von NURDEN, A. T.

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Gene Therapy Targeting Synthesis of Coagulation Factor VIII in Platelets Reduces Bleeding in Canine Hemophilia A von Du, L.M, Franck, H.W.G, Merricks, E.P, Nurden, P, Jensen, E.S, Haberichter, S.L, Hawkins, T.B, Jacobi, P.M, Fang, J, Nichols, T.C, Koukouritaki, S.B, Shi, Q, Nurden, A.T, Montogomery, R.R, Cornetta, K, Wilcox, D.A

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Platelet membrane glycoproteins: historical perspectives von NURDEN, A. T., PHILLIPS, D. R., GEORGE, J. N.

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Analysis of platelet membrane glycoprotein polymorphisms in Glanzmann thrombasthenia showed the French gypsy mutation in the αIIb gene to be strongly linked to the HPA‐1b polymorph... von Jacquelin, B., Tuleja, E., Kunicki, T. J., Nurden, P., Nurden, A. T.

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Rebuttal: the French Gypsy mutation does not give rise to a particularly mild form of Glazmann's thrombasthenia von Nurden, A. T., Nurden, P.

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