MEK 1 inhibition and bleeding in hereditary haemorrhagic telangiectasia by Shovlin, Claire L, Patel, Dilip, Bielowka, Adrianna, Ledermann, Jonathan A, Modarresi, Atieh, Bernabeu-Herrero, Maria E, Aldred, Micheala A, Alsafi, Ali

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Mutational and phenotypic characterization of hereditary hemorrhagic telangiectasia by Shovlin, Claire L., Simeoni, Ilenia, Downes, Kate, Frazer, Zoe C., Megy, Karyn, Bernabeu-Herrero, Maria E., Shurr, Abigail, Brimley, Jennifer, Patel, Dilipkumar, Kell, Loren, Stephens, Jonathan, Turbin, Isobel G., Aldred, Micheala A., Penkett, Christopher J., Ouwehand, Willem H., Jovine, Luca, Turro, Ernest

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Functional filter for whole-genome sequencing data identifies HHT and stress-associated non-coding SMAD4 polyadenylation site variants >5 kb from coding DNA by Xiao, Sihao, Kai, Zhentian, Murphy, Daniel, Li, Dongyang, Patel, Dilip, Bielowka, Adrianna M., Bernabeu-Herrero, Maria E., Abdulmogith, Awatif, Mumford, Andrew D., Westbury, Sarah K., Aldred, Micheala A., Vargesson, Neil, Caulfield, Mark J., Shovlin, Claire L.

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Mutation study of Spanish patients with hereditary hemorrhagic telangiectasia by Fontalba, Ana, Fernandez-L, Africa, García-Alegria, Eva, Albiñana, Virginia, Garrido-Martin, Eva M, Blanco, Francisco J, Zarrabeitia, Roberto, Perez-Molino, Alfonso, Bernabeu-Herrero, Maria E, Ojeda, Maria-Luisa, Fernandez-Luna, Jose L, Bernabeu, Carmelo, Botella, Luisa M

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Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT by Bernabéu-Herrero, Maria E., Patel, Dilipkumar, Bielowka, Adrianna, Zhu, JiaYi, Jain, Kinshuk, Mackay, Ian S., Chaves Guerrero, Patricia, Emanuelli, Giulia, Jovine, Luca, Noseda, Michela, Marciniak, Stefan J., Aldred, Micheala A., Shovlin, Claire L.

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Heterogeneity but individual constancy of epitopes, isotypes and avidity of factor H autoantibodies in atypical hemolytic uremic syndrome by Nozal, Pilar, Bernabéu-Herrero, Maria E., Uzonyi, Barbara, Szilágyi, Ágnes, Hyvärinen, Satu, Prohászka, Zoltán, Jokiranta, T. Sakari, Sánchez-Corral, Pilar, López-Trascasa, Margarita, Józsi, Mihály

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Scientific Business Abstracts by Zimmermann, Jasminka, Vaughan, Michael, Cheshire, Christopher, Li, Zhongwang, Altinok, Selin, De Silvera, Willian, Rodriques, Samuel, Blaber, Elizabeth, Schisler, Jonathan, Masafumi, Muratani, Beheshti, Afshin, Lean, Michael, Sattar, Naveed, Leslie, Wilma, Thom, George, Cook, Sarah, Hatem, Sara, Ford, David V, Sheikh, Aziz, Quint, Jennifer K, Fareed, Rana, Williams, Claire, Bain, Steve, Fraser, Diane, Oram, Richard, Sadeghi-Alavijeh, Omid, Moochhala, Shabbir, Jennings, Rachel, Baker, Syed Murtuza, Zarrineh, Peyman, Al-Banaki, Ali, Mullan, Aoibheann, Goncalves, Maria Alexandra, Hanley, Neil, Menon, Usha, Blundell, Jamie, Bernabeu-Herrero, Maria, Aldred, Michaela, Guerrero, Patricia Chaves, Marciniak, Stefan, Patel, Dilipkumar, Ho, Antonia, Asamaphan, Patawee, Herder, Vanessa, Davis, Chris, Pollock, Louisa, Roy, Kirsty, Divala, Titus, Holden, Matt, Jackson, Celia, MacLean, Alasdair, da Silva Filipe, Ana, Turner, David, Baillie, Kenneth, Horne, Elsie, Parker, Edward, Goldacre, Ben, Sterne, Jonathan, Abrams, Simon, Alhamdi, Yasir, Wang, Guozheng, Mizani, Mehrdad, Pasea, Laura, Corbett, Richard, Gao, He, Hemingway, Harry, Raisi-Estabragh, Zahra, Szabo, Liliana, Altman, Andre, Neubauer, Stefan, Lees, Jennifer, Crowther, Jamie, Gillies, Katie, Dias, Sophie, Nazareth, Dilip, Wat, Dennis, Walshaw, Martin, Lip, Gregory, Bennett, Derrick, Lacey, Ben, Massa, Sofia, Bath, Philip, Mbizvo, Gashirai, Simpson, Colin, Chin, Richard, Wood, Greta K, Tharmaratnam, K, Sargent, B, Ahmad, Z, Rogers, Hc, Dunai, C, Martin, N, Taylor, J P, David, A, Harrison, N, Jackson, T, Nicholson, T, Michael, B D, Paddick, S M, Leek, C

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MP124FAMILY DEFECTS IN FACTOR H/FHRS OF THE COMPLEMENT IN IGA NEPHROPATHY by Olea, Teresa, Bernabeu-Herrero, María E, Rodríguez-Gayo, Lucía, Selgas, Rafael, López-Trascasa, Margarita, Sánchez- Corral, Pilar

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