Treffer 1 - 20 von 48 für Suche 'Rogers, Ella K.', Suchdauer: 1,03s Treffer weiter einschränken
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    Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype-phenotype study in neurofibromatosis type 1 von Koczkowska, Magdalena, Callens, Tom, Chen, Yunjia, Gomes, Alicia, Hicks, Alesha D, Sharp, Angela, Johns, Eric, Uhas, Kim Armfield, Armstrong, Linlea, Bosanko, Katherine Armstrong, Babovic-Vuksanovic, Dusica, Baker, Laura, Basel, Donald G, Bengala, Mario, Bennett, James T, Chambers, Chelsea, Clarkson, Lola K, Clementi, Maurizio, Cortes, Fanny M, Cunningham, Mitch, D'Agostino, M. Daniela, Delatycki, Martin B, Digilio, Maria C, Dosa, Laura, Esposito, Silvia, Fox, Stephanie, Freckmann, Mary-Louise, Fauth, Christine, Giugliano, Teresa, Giustini, Sandra, Goetsch, Allison, Goldberg, Yael, Greenwood, Robert S, Griffis, Cristin, Gripp, Karen W, Gupta, Punita, Haan, Eric, Hachen, Rachel K, Haygarth, Tamara L, Hernandez-Chico, Concepcion, Hodge, Katelyn, Hopkin, Robert J, Hudgins, Louanne, Janssens, Sandra, Keller, Kory, Kelly-Mancuso, Geraldine, Kochhar, Aaina, Korf, Bruce R, Lewis, Andrea M, Liebelt, Jan, Lichty, Angie, Listernick, Robert H, Lyons, Michael J, Maystadt, Isabelle, Ojeda, Mayra Martinez, McDougall, Carey, McGregor, Lesley K, Melis, Daniela, Mendelsohn, Nancy, Nowaczyk, Malgorzata J.M, Ortenberg, June, Panzer, Karin, Pappas, John G, Pierpont, Mary Ella, Piluso, Giulio, Pinna, Valentina, Pivnick, Eniko K, Pond, Dinel A, Powell, Cynthia M, Rogers, Caleb, Shahar, Noa Ruhrman, Rutledge, S. Lane, Saletti, Veronica, Sandaradura, Sarah A, Santoro, Claudia, Schatz, Ulrich A, Schreiber, Allison, Scott, Daryl A, Sellars, Elizabeth A, Sheffer, Ruth, Siqveland, Elizabeth, Slopis, John M, Smith, Rosemarie, Spalice, Alberto, Stockton, David W, Streff, Haley, Theos, Amy, Tomlinson, Gail E, Tran, Grace, Trapane, Pamela L, Trevisson, Eva, Ullrich, Nicole J, Van den Ende, Jenneke, Vergano, Samantha A. Schrier, Wallace, Stephanie E, Wangler, Michael F, Weaver, David D, Yohay, Kaleb H, Zackai, Elaine, Zonana, Jonathan

    Veröffentlicht in HUMAN MUTATION

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    Clinical spectrum of individuals with pathogenic N F1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1 von Koczkowska, Magdalena, Callens, Tom, Chen, Yunjia, Gomes, Alicia, Hicks, Alesha D., Sharp, Angela, Johns, Eric, Uhas, Kim Armfield, Armstrong, Linlea, Bosanko, Katherine Armstrong, Babovic‐Vuksanovic, Dusica, Baker, Laura, Basel, Donald G., Bengala, Mario, Bennett, James T., Chambers, Chelsea, Clarkson, Lola K., Clementi, Maurizio, Cortés, Fanny M., Cunningham, Mitch, D'Agostino, M. Daniela, Delatycki, Martin B., Digilio, Maria C., Dosa, Laura, Esposito, Silvia, Fox, Stephanie, Freckmann, Mary‐Louise, Fauth, Christine, Giugliano, Teresa, Giustini, Sandra, Goetsch, Allison, Goldberg, Yael, Greenwood, Robert S., Griffis, Cristin, Gripp, Karen W., Gupta, Punita, Haan, Eric, Hachen, Rachel K., Haygarth, Tamara L., Hernández‐Chico, Concepción, Hodge, Katelyn, Hopkin, Robert J., Hudgins, Louanne, Janssens, Sandra, Keller, Kory, Kelly‐Mancuso, Geraldine, Kochhar, Aaina, Korf, Bruce R., Lewis, Andrea M., Liebelt, Jan, Lichty, Angie, Listernick, Robert H., Lyons, Michael J., Maystadt, Isabelle, Martinez Ojeda, Mayra, McDougall, Carey, McGregor, Lesley K., Melis, Daniela, Mendelsohn, Nancy, Nowaczyk, Malgorzata J.M., Ortenberg, June, Panzer, Karin, Pappas, John G., Pierpont, Mary Ella, Piluso, Giulio, Pinna, Valentina, Pivnick, Eniko K., Pond, Dinel A., Powell, Cynthia M., Rogers, Caleb, Ruhrman Shahar, Noa, Rutledge, S. Lane, Saletti, Veronica, Sandaradura, Sarah A., Santoro, Claudia, Schatz, Ulrich A., Schreiber, Allison, Scott, Daryl A., Sellars, Elizabeth A., Sheffer, Ruth, Siqveland, Elizabeth, Slopis, John M., Smith, Rosemarie, Spalice, Alberto, Stockton, David W., Streff, Haley, Theos, Amy, Tomlinson, Gail E., Tran, Grace, Trapane, Pamela L., Trevisson, Eva, Ullrich, Nicole J., Van den Ende, Jenneke, Schrier Vergano, Samantha A., Wallace, Stephanie E., Wangler, Michael F., Weaver, David D., Yohay, Kaleb H., Zackai, Elaine, Zonana, Jonathan

    Veröffentlicht in Human mutation

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    Prespecified dose-response analysis for A Very Early Rehabilitation Trial (AVERT) von Bernhardt, Julie, Churilov, Leonid, Ellery, Fiona, Collier, Janice, Chamberlain, Jan, Langhorne, Peter, Lindley, Richard I., Moodie, Marj, Dewey, Helen, Thrift, Amanda G., Donnan, Geoff, Bernhardt, Julie, Churilov, Leonid, Collier, Janice, Dewey, Helen, Donnan, Geoffrey, Ellery, Fiona, Langhorne, Peter, Lindley, Richard, Moodie, Marjory, Parsons, Brooke, Thrift, Amanda, Investigators MIs, Main, Indredavik, Bent, Askim, Torunn, Bath, Phillip, Bladin, Christopher, Reid, Christopher, Read, Stephen, Said, Cathy, Middleton, Sandy, Frayne, Judith, Srikanth, Velandai, Bernhardt, Australia: Julie, Carter, Robert, Donnan, Geoff, Wu, Olivia, Claire Ritchie, Matthew Walters, Smith, Lorraine, Ashburn, Anne, Rodgers, Helen, Rogers, Helen, Lennon, Sheila, Power, Michael, Hameed, Shahul, Pavanni, Ratnagopal, Lim, Peter, Tan, Dawn, Brewer, Tim, Haritos, Nick, Leong, Edwin, Li, Cecilia, NayWin, Caesar, Nicol, Marcus, Olenka, Liudmyla, Quang, Li Chun, Hope, Silvia, Sheppard, Lauren, Teo, Kiusiang Tay, Cumming, Toby, Linden, Thomas, Borschmann, Karen, Chamberlain, Jan, Occhiodoro, Teresa, Palfreeman, Helen, Purvis, Tara, Sirgo, Bernadette, Tiliacos, Nick, Van Holsteyn, John, Zhao, Henry, Armstrong, Beverly, Craig, Louise, Graham, Fiona, Legg, Lynn, Morrison, Rosemary, Moorhead, Heather, O’Donohue, Lorraine, Rogers, Susan, Smith, Myra, Forshaw, Denise, Fitzgerald, Jane, Hibbert, E, Melling, R, Petrolo, S, Purvis, T, Williamson MIs, H, Adams, P, Augoustakis, L, Batcheler, S, Berney, S, Cobani, V, Cohen, B, Dewey, H, Gangi, S, Giofre, N, Gordon, C, Hegarty, L, Hindson, M, Horvath, F, Kalinowski, S

    Veröffentlicht in Neurology

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