Treffer 1 - 13 von 13 für Suche 'Van, Allison Alicia', Suchdauer: 0,94s Treffer weiter einschränken
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    Characteristics of the Ontario Neurodegenerative Disease Research Initiative cohort von Sunderland, Kelly M., Beaton, Derek, Arnott, Stephen R., Kleinstiver, Peter, Kwan, Donna, Lawrence‐Dewar, Jane M., Ramirez, Joel, Tan, Brian, Bartha, Robert, Black, Sandra E., Borrie, Michael, Brien, Donald, Casaubon, Leanne K., Coe, Brian C., Cornish, Benjamin, Dilliott, Allison A., Dowlatshahi, Dar, Finger, Elizabeth, Fischer, Corinne, Frank, Andrew, Fraser, Julia, Freedman, Morris, Greenberg, Barry, Grimes, David A., Hassan, Ayman, Hatch, Wendy, Hegele, Robert A., Hudson, Christopher, Jog, Mandar, Kumar, Sanjeev, Lang, Anthony, Levine, Brian, Lou, Wendy, Mandzia, Jennifer, Marras, Connie, McIlroy, William, Montero‐Odasso, Manuel, Munoz, David G., Munoz, Douglas P., Orange, Joseph B., Park, David S., Pasternak, Stephen H., Pieruccini‐Faria, Frederico, Rajji, Tarek K., Roberts, Angela C., Robinson, John F., Rogaeva, Ekaterina, Sahlas, Demetrios J., Saposnik, Gustavo, Scott, Christopher J.M., Seitz, Dallas, Shoesmith, Christen, Steeves, Thomas D.L., Strong, Michael J., Strother, Stephen C., Swartz, Richard H., Symons, Sean, Tang‐Wai, David F., Tartaglia, Maria Carmela, Troyer, Angela K., Turnbull, John, Zinman, Lorne, McLaughlin, Paula M., Masellis, Mario, Binns, Malcolm A., Abrahao, Agessandro, Adamo, Sabrina, Berezuk, Courtney, Black, Alanna, Breen, David P., Bulman, Dennis, Chen, Ying, El‐Defrawy, Sherif, Farhan, Sali, Ghani, Mahdi, Gonder, John, Haddad, Seyyed M. H., Holmes, Melissa, Huang, Jeff, Leontieva, Elena, Mandelcorn, Efrem, Margolin, Edward, Nanayakkara, Nuwan, Ozzoude, Miracle, Peltsch, Alicia J., Pollock, Bruce, Raamana, Pradeep, Rashkovan, Natalie, Yanina, Southwell, Alisia, Sujanthan, Sujeevini, Tayyari, Faryan, Van Ooteghem, Karen, Woulfe, John, Zamyadi, Mojdeh, Zou, Guangyong

    Veröffentlicht in Alzheimer's & dementia

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    Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848 von Koczkowska, Magdalena, Chen, Yunjia, Callens, Tom, Gomes, Alicia, Sharp, Angela, Johnson, Sherrell, Hsiao, Meng-Chang, Chen, Zhenbin, Balasubramanian, Meena, Barnett, Christopher P, Becker, Troy A, Ben-Shachar, Shay, Bertola, Debora R, Blakeley, Jaishri O, Burkitt-Wright, Emma M.M, Callaway, Alison, Crenshaw, Melissa, Cunha, Karin S, Cunningham, Mitch, D'Agostino, Maria D, Dahan, Karin, De Luca, Alessandro, Destrée, Anne, Dhamija, Radhika, Eoli, Marica, Evans, D. Gareth R, Galvin-Parton, Patricia, George-Abraham, Jaya K, Gripp, Karen W, Guevara-Campos, Jose, Hanchard, Neil A, Hernández-Chico, Concepcion, Immken, LaDonna, Janssens, Sandra, Jones, Kristi J, Keena, Beth A, Kochhar, Aaina, Liebelt, Jan, Martir-Negron, Arelis, Mahoney, Maurice J, Maystadt, Isabelle, McDougall, Carey, McEntagart, Meriel, Mendelsohn, Nancy, Miller, David T, Mortier, Geert, Morton, Jenny, Pappas, John, Plotkin, Scott R, Pond, Dinel, Rosenbaum, Kenneth, Rubin, Karol, Russell, Laura, Rutledge, Lane S, Saletti, Veronica, Schonberg, Rhonda, Schreiber, Allison, Seidel, Meredith, Siqveland, Elizabeth, Stockton, David W, Trevisson, Eva, Ullrich, Nicole J, Upadhyaya, Meena, van Minkelen, Rick, Verhelst, Helene, Wallace, Margaret R, Yap, Yoon-Sim, Zackai, Elaine, Zonana, Jonathan, Zurcher, Vickie, Claes, Kathleen, Martin, Yolanda, Korf, Bruce R, Legius, Eric, Messiaen, Ludwine


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