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    Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis by Dominguez, Fernando, Lopes, Luis Rocha, Ochoa, Juan Pablo, Barriales-Villa, Roberto, Climent, Vicente, Linschoten, Marijke, Tiron, Coloma, Chiriatti, Chiara, Marques, Nuno, Rasmussen, Torsten B., Espinosa, María Ángeles, Cesar, Sergi, Field, Ella, Garcia-Pinilla, Jose M., Muir, Alison R., Roberts, Angharad M., Santas, Enrique, Zorio, Esther, Peña-Peña, Maria Luisa, Navarro, Marina, Fernandez, Adrian, Palomino-Doza, Julian, Azevedo, Olga, Lorenzini, Massimiliano, García-Álvarez, Maria I., Bento, Dina, Jensen, Morten K., Méndez, Irene, Pezzoli, Laura, Sarquella-Brugada, Georgia, Campuzano, Oscar, Gonzalez-Lopez, Esther, Kaski, Juan Pablo, Brugada, Ramon, Monserrat, Lorenzo, Olivotto, Iacopo, Elliott, Perry M., Garcia-Pavia, Pablo, Rasmussen, Torsten B., Jensen, Morten K., Larrañaga-Moreira, Jose María, Alonso-García, Diego, Cárdenas-Reyes, Ivonne Johana, Cicerchia, Marcos, García-Ferro, German, García-Hernández, Soledad, Monserrat, Lorenzo, Nöel-Bröger, María, Ochoa, Juan Pablo, Ortiz, Martin, Bento, Dina, Mota, Teresa, Fernandes, Raquel, Costa, Hugo, Marques, Nuno, Climent, Vicente, García-Álvarez, Maria I., Cesar, Sergi, Sarquella-Brugada, Georgia, Muir, Alison R., Pezzoli, Laura, Quarta, Giovanni, Fernandez, Adrian, Field, Ella, Azevedo, Olga, Santas, Enrique, Chiriatti, Chiara, Brugada, Ramon, Campuzano, Oscar, Doza, Julian Palomino, Salguero-Bodes, Rafael, Valverde-Gomez, Maria, Espinosa, Maria Angeles, Mendez, Irene, Cobo-Marcos, Marta, Domínguez, Fernando, Garcia-Pavia, Pablo, González-López, Esther, Segovia-Cubero, Javier, Vilches, Silvia, Garcia-Pinilla, Jose Manuel, López-Garrido, Miguel, Abad, Victoria Doncel, Navarro, Marina, Sabater-Molina, Maria, Gimeno-Blanes, Juan Ramón, Peña-Peña, Maria Luisa, Mogensen, Jens, Barton, Paul J., Cook, Stuart A., Roberts, Angharad M., Ware, James S., Lopes, Luis Rocha, Lorenzini, Massimiliano, Syrris, Petros, Truszkowska, Grażyna, Michalak, Ewa, Asselbergs, Folkert, Baas, Annette F., Dooijes, Dennis

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    Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia by Reich, Adi, Cross, J. Helen, Scheffer, Ingrid E., Krishnappa, Netravathi, Awada, Jana, Baralle, Diana, Bernhard, Birgitta, Clasper, Susan, Clayton-Smith, Jill, Cresswell, Lara, Donaldson, Alan, Ellis, Ian, Gaunt, Lorraine, He, Liu, Hewitt, Sarah, Hurst, Jane, Kirk, Claire, Kivuva, Emma, Kumar, Dhavendra, Mansour, Sahar, McCann, Emma, McKee, Shane, Mugalaasi, Hood, Murphy, Helen, Newbury-Ecob, Ruth, Pilz, Daniela T., Pollard, Martin, Pridham, Abigail, Saggar, Anand, Scott, Richard, Shearing, Emma, Smithson, Sarah, Sneddon, Linda, Suri, Mohnish, Tatton-Brown, Kate, Thomson, Jenny, Torokwa, Audrey, Varghese, Vinod, Yau, Michael, Artigas, Maria Soler, Boustred, Chris, Evans, David, Flicek, Paul, Hart, Deborah, Langford, Cordelia, Lawson, Daniel, Li, Rui, O'Donnovan, Michael, Parker, Victoria, Parr, Jeremy R., Paunio, Tiina, Rehnström, Karola, Sun, Jianping, Suvisaari, Jaana, Tachmazidou, Ionna, Williamson, Kathleen A., Wong, Kim, Alachkar, Hana, Ambegaonkar, Gautum, Attwood, Antony, Austin, Steve, Bennett, David, Bibi, Shahnaz, Bleda, Marta, Boggard, Harm, Bradley, John R., Browning, Michael, Clement, Emma, Doffinger, Rainer, Drewe, Elizabeth, Frary, Amy, Ghataorhe, Pavandeep K., Greenhalgh, Alan, Hackett, Scott, Hadinnapola, Charaka, Heemskerk, Johan W.M., Humbert, Marc, James, Roger, Krishnakumar, Deepa, Lawrie, Allan, Lentaigne, Claire, Maimaris, Jesmeen, Maw, Anna, Megy, Karyn, Moledina, Shahin, Morrell, Nicholas, Nejentsev, Sergey, Polwarth, Gary, Quinti, Isabella, Raymond, F. Lucy, Samarghitean, Crina, Sanchis-Juan, Alba, Southgate, Laura, Stauss, Hans, Thrasher, Adrian, Trembath, Richard, Turro, Ernest, Williamson, Catherine, Yeatman, Nigel, Millichap, John J.

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