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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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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P080 Compound heterozygous mutations in gene encoding Protein C as a cause of familial Cerebral Palsy in siblings von Fong, C.Y, Mumford, A.D, Likeman, M.J, Jardine, P.E

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Laboratory monitoring of P2Y12 inhibitors: communication from the SSC of the ISTH von Frelinger, A. L., Gachet, C., Mumford, A. D., Noris, P., Mezzano, D., Harrison, P., Gresele, P.

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Platelet dysfunction associated with the novel Trp29Cys thromboxane A2 receptor variant von Mumford, A. D., Nisar, S., Darnige, L., Jones, M. L., Bachelot‐Loza, C., Gandrille, S., Zinzindohoue, F., Fischer, A.‐M., Mundell, S. J., Gaussem, P.

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Rapid genetic diagnosis of heritable platelet function disorders with next‐generation sequencing: proof‐of‐principle with Hermansky–Pudlak syndrome von JONES, M. L., MURDEN, S. L., BEM, D., MUNDELL, S. J., GISSEN, P., DALY, M. E., WATSON, S. P., MUMFORD, A. D.

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More on: endoplasmic reticulum loop VKORC1 substitutions cause warfarin resistance but do not diminish gamma‐carboxylation of the vitamin K‐dependent coagulation factors von HARRINGTON, D. J., SIDDIQ, S., ALLFORD, S. L., SHEARER, M. J., MUMFORD, A. D.

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How useful is light transmission platelet aggregometry for the diagnosis of bleeding disorders? von MUMFORD, A. D.

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Pharmacodynamic resistance to warfarin is associated with nucleotide substitutions inVKORC1 von HARRINGTON, D.J., GORSKA, R., WHEELER, R., DAVIDSON, S., MURDEN, S., MORSE, C., SHEARER, M.J., MUMFORD, A.D.

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Spectroscopic and microscopic characterisation of microbial biofouling on aircraft fuel tanks von Gómez-Bolívar, J, Warburton, M.P, Mumford, A.D, Mujica-Alarcón, J.F, Anguilano, L, Onwukwe, U, Barnes, J, Chronopoulou, M, Ju-Nam, Y, Thornton, S.F, Rolfe, S.A, Ojeda, J.J

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Hereditary Hyperferritinemia-Cataract Syndrome: Two Novel Mutations in the L-Ferritin Iron-Responsive Element von Mumford, A.D., Vulliamy, T., Lindsay, J., Watson, A.

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Hereditary hyperferritinemia cataract syndrome: ocular, genetic, and biochemical findings von Ismail, A R, Lachlan, K L, Mumford, A D, Temple, I K, Hodgkins, P R

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Hereditary Hyperferritinemia-Cataract Syndrome: Two Novel Mutations in the L-Ferritin Iron-Responsive Element von Mumford, A.D., Vulliamy, T., Lindsay, J., Watson, A.

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Diversity and impact of rare variants in genes encoding the platelet G protein-coupled receptors von Jones, M.L, Norman, J.E, Morgan, N.V, Mundell, S.J, Lordkipanidze, M, Lowe, G.C, Daly, M.E, Simpson, M.A, Drake, S, Watson, S.P, Mumford, A.D, UKGAPPS

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Hamartomas of the breast: six novel diagnostic features in three-dimensional thick sections von DAVIES, J.D., KULKA, J., MUMFORD, A.D., ARMSTRONG, J.S., WELLS, C.A.

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Minimal factor XIII activity level to prevent major spontaneous bleeds von Menegatti, M., Palla, R., Boscarino, M., Bucciarelli, P., Muszbek, L., Katona, E., Makris, M., Peyvandi, F., Halimeh, S., Lachmann, B., Bidlingmaier, C., Platokouki, H., Pergantou, H., Siboni, S. M., Schutgens, R. E. G., Borhany, M., Fatima, N., Mikovic, D., Saracevic, M., Moerloose, P., Casini, A., Ozdemir, N., Ay, Y., Mumford, A., Harvey, A., Payne, J., Shapiro, A. D., Williamson, A., Chapin, J., Hsu, F.

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Purification and characterization of active human interleukin-1 beta-converting enzyme from THP.1 monocytic cells von Miller, D.K., Ayala, J.M., Egger, L.A., Raju, S.M., Yamin, T.T., Ding, G.J., Gaffney, E.P., Howard, A.D., Palyha, O.C., Rolando, A.M.

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Potential of the mite-pathogenic fungus Neozygites floridana (Entomophthorales: Neozygitaceae) for control of the cassava green mite Mononychellus tanajoa (Acari: Tetranychidae) von Elliot, S.L., de Moraes, G.J., Delalibera, I., da Silva, C.A.D., Tamai, M.A., Mumford, J.D.

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Variability in the analysis of a single neuroimaging dataset by many teams von Botvinik-Nezer, R., Dreber, A., Johannesson, M., Kirchler, M., Mumford, J.A., Adcock, R.A., Avesani, P., Bakst, L., Ball, S., Beaton, D., Berkers, R.M.W.J., Biswal, B.B., Bobadilla-Suarez, S., Bottenhorn, K.L., Braem, S., Camilleri, J.A., Castrellon, J.J., Cecchetti, L., Cieslik, E.C., Czoschke, S., Dadi, K., Davis, C.P., Luca, A.D., Delgado, M.R., Dennison, J.B., , X. di, Dickie, E.W., Durnez, J., Fricke, G.M., Fu, S.G., Galvan, A., Glerean, E., Goeman, J.J., Golowin, S.A.E., Grady, C.L., Green, M.A., Moreira, J.F.G., Hakimi, S., Hancock, R., Herholz, P., Heunis, S., Hogeveen, J., Hu, C.P., Hughes, M.E., Iacovella, V., Isik, A.I., Johnstone, T., Joseph, M.J.E., Kassinopoulos, M., Koba, C., Kucukboyaci, N.E., Leemans, A., Li, F.R., Lim, P.C., Lintz, E.N., Love, B.C., Mack, M.L., McDonald, K., Leal, A.M.S., Meyer, B., Meyer, K.N., Mihai, G., Notter, M.P., Olivetti, E., Onicas, A.I., Papale, P., Perez, A., Pischedda, D., Poline, J.B., Prystauka, Y., Ray, S., Reuter-Lorenz, P.A., Reynolds, R.C., Ricciardi, E., Rodriguez-Thompson, A.M., Salo, T., Samanez-Larkin, G.R., Sanz-Morales, E., Sheridan, M.A., Silvers, J.A., Skagerlund, K., Smith, A., Smith, D.V., Steinkamp, S.R., Thirion, B., Thorp, J.N., Tinghog, G., Tisdall, L., Tresols, J.J.T., Tozzi, L., Truong, V., Veer, A.E. van 't, Verguts, T., Vettel, J.M., Weis, S., White, D.J., Wisniewski, D., Yearling, E.A., Zhang, L., Poldrack, R.A.

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Variability in the analysis of a single neuroimaging dataset by many teams von Botvinik-Nezer, R., Dreber, A., Johannesson, M., Kirchler, M., Mumford, J.A., Adcock, R.A., Avesani, P., Bakst, L., Ball, S., Beaton, D., Berkers, R.M.W.J., Biswal, B.B., Bobadilla-Suarez, S., Bottenhorn, K.L., Braem, S., Camilleri, J.A., Castrellon, J.J., Cecchetti, L., Cieslik, E.C., Czoschke, S., Dadi, K., Davis, C.P., Luca, A.D., Delgado, M.R., Dennison, J.B., Dickie, E.W., Donnat, C.L., Durnez, J., Fricke, G.M., Fu, S.G., Galvan, A., Glerean, E., Goeman, J.J., Golowin, S.A.E., Grady, C.L., Green, M.A., Moreira, J.F.G., Hakimi, S., Hancock, R., Herholz, P., Heunis, S., Hogeveen, J., Hu, C.P., Hughes, M.E., Iacovella, V., Isik, A.I., Johnstone, T., Joseph, M.J.E., Kassinopoulos, M., Koba, C., Kucukboyaci, N.E., Leemans, A., Li, F.R., Lim, P.C., Lintz, E.N., Love, B.C., Mack, M.L., McDonald, K., Leal, A.M.S., Meyer, B., Meyer, K.N., Mihai, G., Notter, M.P., Olivetti, E., Onicas, A.I., Papale, P., Perez, A., Pischedda, D., Poline, J.B., Prystauka, Y., Ray, S., Reuter-Lorenz, P.A., Reynolds, R.C., Ricciardi, E., Rodriguez-Thompson, A.M., Salo, T., Samanez-Larkin, G.R., Sanz-Morales, E., Sheridan, M.A., Silvers, J.A., Skagerlund, K., Smith, A., Smith, D.V., Steinkamp, S.R., Thirion, B., Thorp, J.N., Tinghog, G., Tisdall, L., Tresols, J.J.T., Tozzi, L., Truong, V., Verguts, T., Vettel, J.M., Vijayarajah, S., Weis, S., White, D.J., Wisniewski, D., Yearling, E.A., Zhang, L., Poldrack, R.A.

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