Efficacy of stroke prevention in atrial fibrillation: a way of improvement

di Aktaa, Suleman, Garg, Anshu, Ackroyd, Sam, Dobrzanski, Stan, Smith, Paul, Atkins, Carol
Pubblicato in Future Hosp J (2015)

SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage

di Clifford, Ruth, Louis, Tania, Robbe, Pauline, Ackroyd, Sam, Burns, Adam, Timbs, Adele T., Wright Colopy, Glen, Dreau, Helene, Sigaux, Francois, Judde, Jean Gabriel, Rotger, Margalida, Telenti, Amalio, Lin, Yea-Lih, Pasero, Philippe, Maelfait, Jonathan, Titsias, Michalis, Cohen, Dena R., Henderson, Shirley J., Ross, Mark T., Bentley, David, Hillmen, Peter, Pettitt, Andrew, Rehwinkel, Jan, Knight, Samantha J. L., Taylor, Jenny C., Crow, Yanick J., Benkirane, Monsef, Schuh, Anna
Pubblicazione 2014

Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study

di Rice, Gillian I, Forte, Gabriella M A, Szynkiewicz, Marcin, Chase, Diana S, Aeby, Alec, Abdel-Hamid, Mohamed S, Ackroyd, Sam, Allcock, Rebecca, Bailey, Kathryn M, Balottin, Umberto, Barnerias, Christine, Bernard, Genevieve, Bodemer, Christine, Botella, Maria P, Cereda, Cristina, Chandler, Kate E, Dabydeen, Lyvia, Dale, Russell C, De Laet, Corinne, De Goede, Christian G E L, del Toro, Mireia, Effat, Laila, Enamorado, Noemi Nunez, Fazzi, Elisa, Gener, Blanca, Haldre, Madli, Lin, Jean-Pierre S-M, Livingston, John H, Lourenco, Charles Marques, Marques, Wilson, Oades, Patrick, Peterson, Pärt, Rasmussen, Magnhild, Roubertie, Agathe, Schmidt, Johanna Loewenstein, Shalev, Stavit A, Simon, Rogelio, Spiegel, Ronen, Swoboda, Kathryn J, Temtamy, Samia A, Vassallo, Grace, Vilain, Catheline N, Vogt, Julie, Wermenbol, Vanessa, Whitehouse, William P, Soler, Doriette, Olivieri, Ivana, Orcesi, Simona, Aglan, Mona S, Zaki, Maha S, Abdel-Salam, Ghada M H, Vanderver, Adeline, Kisand, Kai, Rozenberg, Flore, Lebon, Pierre, Crow, Yanick J
Pubblicato in Lancet Neurol (2013)

A HaemSTAR-led, UK-wide ‘flash-mob’ audit of ­intravenous immunoglobulin use in immune ­thrombocytopenia

di Nicolson, Phillip, Perry, Rita, Fisher, Amelia, Scott, Gemma, Magill, Laura, Chan-Lam, Dominique, Thorpe, Alice, Macheta, Mac, Carter-Brzezinski, Luke, Ackroyd, Sam, Katumba, Alvin, Bradbury, Charlotte, Jen, Sheila, Camillieri, Marquita, Besser, Martin, Bull, Tom, Leighton, Katherine, Ayalew, Yezenash, Willan, John, Watson, Edmund, Oshinyemi, Pamela, Upadhye, Yogesh, Pickard, Keir, Swart-Rimmer, Imogen, Knott, Chloe, Chown, Sally, Crolla, Francesca, Quinn, Daire, McLeod-Kennedy, Lindsay, Oun, Hajer, McDermott, Christopher, Walker, Mairi, Mullally, Ryan, Herlihy, Naoimh, Shah, Gulnaz, Doyle, Andrew, Robinson, Susan, Sayar, Zara, Pryor, Rebecca, Peet, Chris, Shenouda, Amir, Venkatadasari, Indrani, Cartier, Jorge, Akay, Melek, Tsitsikas, Dimitris, Sivapalaratnam, Suthesh, Cooper, Nichola, Lentaigne, Claire, Bailey, Chris, Xu, Dan Mei, Janum, Sine, Mohan, Arunodaya, Kimberger, Katja, Kgologolo, Maipelo, Sevillano, Belen, Hanina, Sophie, Danga, Akila, Mustafa, Chira, Wilding, Charlotte, Trikha, Roochi, Wang, Han, Crossette-Thambiah, Cristina, Hastings, Andrew, Sreedhara, Sree, Wright, David, Batey, Laura, Atkin, Abigail, Davis, Sarah, Jaafar, Sarah, Ejaz, Ayesha, Biss, Tina, Swieton, Jennifer, Noh, Mohd Sharin Mohd, Gibson, Holly, Freeman, Tanya, Badaguma, Upekha, Kreze, Olivia, Kirkpatrick, Suriya, Suntharalingam, Surenthini, Kmonicek, Miroslab, Joffe, Michael, Halperin, Dan, Desborough, Michael, Rampotas, Alexandros, Dhillon, Elissa, Greaves, Paul, Blacker, Edward, Aiken, Laura, Boot, Jesca, Prasannan, Nithya, Kerr, Jonathan, Martin, Abi, Wexler, Sarah, Burney, Claire, Melly, Michelle, Nolan, Regina, Hipkins, Rupert, Kaddam, Israa, Elmoamly, Shereef, Darlow, Jennifer, Plews, Dianne, Shrubsole, Caroline, Loizou, Eleana, Garth, Louise, Peter, Hina, Wolf, Julia, Walia, Shivali, MacDonald, Vickie, Zaidi, Abbas, Dunk, Robert, Miah, Haroon, Miah, Atiqa, Tucker, David, Skinner, Thomas, Cakmak, Seda, Cakmak, Ipek, Hussein, Hayder, Buka, Richard, Wilson, Lydia, Talbot, Georgina, Qureshi, Hafiz, Wharin, Sarah, Dillon, Anna, Bailiff, Benjamin, McIlroy, Graham, Murray, Duncan, Seymour, Frances, Graham, Jane, Harrison, Samuel, Salhan, Beena, Sharpe, David, Thomas, Wayne, McCulloch, Rory, Crosbie, Nicola, Lowe, Gillian, Hill, Quentin
Pubblicato in Clin Med (Lond) (2019)

Characterization of Human Disease Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

di Crow, Yanick J., Chase, Diana S., Schmidt, Johanna Lowenstein, Szynkiewicz, Marcin, Forte, Gabriella M.A., Gornall, Hannah L., Oojageer, Anthony, Anderson, Beverley, Pizzino, Amy, Helman, Guy, Abdel-Hamid, Mohamed S., Abdel-Salam, Ghada M., Ackroyd, Sam, Aeby, Alec, Agosta, Guillermo, Albin, Catherine, Allon-Shalev, Stavit, Arellano, Montse, Ariaudo, Giada, Aswani, Vijay, Babul-Hirji, Riyana, Baildam, Eileen M., Bahi-Buisson, Nadia, Bailey, Kathryn M., Barnerias, Christine, Barth, Magalie, Battini, Roberta, Beresford, Michael W., Bernard, Geneviève, Bianchi, Marika, de Villemeur, Thierry Billette, Blair, Edward M., Bloom, Miriam, Burlina, Alberto B., Carpanelli, Maria Luisa, Carvalho, Daniel R., Castro-Gago, Manuel, Cavallini, Anna, Cereda, Cristina, Chandler, Kate E., Chitayat, David A., Collins, Abigail E., Corcoles, Concepcion Sierra, Cordeiro, Nuno J.V., Crichiutti, Giovanni, Dabydeen, Lyvia, Dale, Russell C., D’Arrigo, Stefano, De Goede, Christian G.E.L., De Laet, Corinne, De Waele, Liesbeth M.H., Denzler, Ines, Desguerre, Isabelle, Devriendt, Koenraad, Di Rocco, Maja, Fahey, Michael C., Fazzi, Elisa, Ferrie, Colin D., Figueiredo, António, Gener, Blanca, Goizet, Cyril, Gowrinathan, Nirmala R., Gowrishankar, Kalpana, Hanrahan, Donncha, Isidor, Bertrand, Kara, Bülent, Khan, Nasaim, King, Mary D., Kirk, Edwin P., Kumar, Ram, Lagae, Lieven, Landrieu, Pierre, Lauffer, Heinz, Laugel, Vincent, La Piana, Roberta, Lim, Ming J., Lin, Jean-Pierre S.-M., Linnankivi, Tarja, Mackay, Mark T., Marom, Daphna R., Lourenço, Charles Marques, McKee, Shane A., Moroni, Isabella, Morton, Jenny E.V., Moutard, Marie-Laure, Murray, Kevin, Nabbout, Rima, Nampoothiri, Sheela, Nunez-Enamorado, Noemi, Oades, Patrick J., Olivieri, Ivana, Ostergaard, John R., Pérez-Dueñas, Belén, Prendiville, Julie S., Ramesh, Venkateswaran, Rasmussen, Magnhild, Régal, Luc, Ricci, Federica, Rio, Marlène, Rodriguez, Diana, Roubertie, Agathe, Salvatici, Elisabetta, Segers, Karin A., Sinha, Gyanranjan P., Soler, Doriette, Spiegel, Ronen, Stödberg, Tommy I., Straussberg, Rachel, Swoboda, Kathryn J., Suri, Mohnish, Tacke, Uta, Tan, Tiong Y., Naude, Johann te Water, Teik, Keng Wee, Thomas, Maya Mary, Till, Marianne, Tonduti, Davide, Valente, Enza Maria, Van Coster, Rudy Noel, van der Knaap, Marjo S., Vassallo, Grace, Vijzelaar, Raymon, Vogt, Julie, Wallace, Geoffrey B., Wassmer, Evangeline, Webb, Hannah J., Whitehouse, William P., Whitney, Robyn N., Zaki, Maha S., Zuberi, Sameer M., Livingston, John H., Rozenberg, Flore, Lebon, Pierre, Vanderver, Adeline, Orcesi, Simona, Rice, Gillian I.
Pubblicato in Am J Med Genet A (2015)