Search Results - Nandagudi, A.

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    A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis by Vaglio, Augusto, Mackie, Sarah L., Hernández-Rodríguez, José, Monach, Paul A., Castañeda, Santos, Solans, Roser, Morado, Inmaculada C., Narváez, Javier, Pease, Colin T., Dasgupta, Bhaskar, Watts, Richard, Khalidi, Nader, Ytterberg, Steven, Boiardi, Luigi, Beretta, Lorenzo, Govoni, Marcello, Bonatti, Francesco, Witte, Torsten, Schönau, Verena, Papo, Thomas, Haroche, Julien, Mahr, Alfred, Molberg, Øyvind, Voskuyl, Alexandre, Brouwer, Elisabeth, Daikeler, Thomas, Berger, Christoph T., Molloy, Eamonn S., Blockmans, Daniel, Lie, Benedicte A., Mclaren, Paul, Wijmenga, Cisca, Allanore, Yannick, Koeleman, Bobby P.C., Callejas, José Luis, Caminal-Montero, Luis, Corbera-Bellalta, Marc, de Miguel, Eugenio, López, J. Bernardino Díaz, Gómez-Vaquero, Carmen, Guijarro-Rojas, Mercedes, Hidalgo-Conde, Ana, Marí-Alfonso, Begoña, Berriochoa, Agustín Martínez, Zapico, Aleida Martínez, Miranda-Filloy, José A., Monfort, Jordi, Ortego-Centeno, Norberto, Pérez-Conesa, Mercedes, Prieto-González, Sergio, Fernández, Raquel Ríos, Sánchez-Martín, Julio, Sopeña, Bernardo, Unzurrunzaga, Ainhoa, Gough, Andrew, Isaacs, John D., McHugh, Neil, Hordon, Lesley, Kamath, Sanjeet, Patel, Yusuf, Yee, Cee-Seng, Nandi, Pradip, Nandagudi, Anupama, Jarrett, Stephen, Levy, Sarah, Mollan, Susan, Salih, Abdel, Wordsworth, Oliver, Sanders, Emma, Gill, Anne, Carr, Lisa, Routledge, Christine, Culfear, Karen, James, Lynne, Spimpolo, Jenny, Kempa, Andy, Masqood, Zahira, Wood, Rose, Rashid, Lubna Haroon, Robinson, James I., Morgan, Mike, Sorensen, Louise, Taylor, John, Carette, Simon, Chung, Sharon, Cuthbertson, David, Forbess, Lindsy J., Gewurz-Singer, Ora, Hoffman, Gary S., Maksimowicz-McKinnon, Kathleen M., Pagnoux, Christian, Seo, Philip, Specks, Ulrich, Spiera, Robert F., Sreih, Antoine, Barrett, Jennifer H., Merkel, Peter A., Morgan, Ann W., González-Gay, Miguel A., Martín, Javier

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    Case Reports 1. A Late Presentation of Loeys-Dietz Syndrome: Beware of TGF  Receptor Mutations in Benign Joint Hypermobility by Mehta, P., Holder, S., Fisher, B., Vincent, T., Nadesalingam, K., Maciver, H., Shingler, W., Bakshi, J., Hassan, S., D'Cruz, D., Chan, A., Litwic, A. E., McCrae, F., Seth, R., Nandagudi, A., Jury, E., Isenberg, D., Karjigi, U., Paul, A., Rees, F., O'Dowd, E., Kinnear, W., Johnson, S., Lanyon, P., Stevens, R., Narayan, N., Marguerie, C., Robinson, H., Ffolkes, L., Worsnop, F., Ostlere, L., Kiely, P., Dharmapalaiah, C., Hassan, N., Bharadwaj, A., Skibinska, M., Gendi, N., Davies, E. J., Akil, M., Kilding, R., Ramachandran Nair, J., Walsh, M., Farrar, W., Thompson, R. N., Borukhson, L., McFadyen, C., Singh, D., Rajagopal, V., Chan, A. M. L., Wearn Koh, L., Christie, J. D., Croot, L., Gayed, M., Disney, B., Singhal, S., Grindulis, K., Reynolds, T. D., Conway, K., Williams, D., Quin, J., Dean, G., Churchill, D., Walker-Bone, K. E., Goff, I., Reynolds, G., Grove, M., Patel, P., Lazarus, M. N., Roncaroli, F., Gabriel, C., Kinderlerer, A. R., Nikiphorou, E., Hall, F. C., Bruce, E., Gray, L., Krutikov, M., Wig, S., Bruce, I., D'Agostino, M. A., Wakefield, R., Berner Hammer, H., Vittecoq, O., Galeazzi, M., Balint, P., Filippucci, E., Moller, I., Iagnocco, A., Naredo, E., Ostergaard, M., Gaillez, C., Kerselaers, W., Van Holder, K., Le Bars, M., Stone, M. A., Williams, F., Wolber, L., Karppinen, J., Maatta, J., Thompson, B., Atchia, I.

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