Development of a novel biopolymer surrogate for studying Cryptosporidium parvum removal in sand media von Ariyadasa, Sujani, Sitthirit, Panan, Sutton, Richard, de Vries, Tanya, Billington, Craig, Pang, Liping

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Common data elements for arthrogryposis multiplex congenita: An international framework von Nematollahi, Shahrzad, Dieterich, Klaus, Filges, Isabel, De Vries, Johanna I. P., Van Bosse, Harold, Natera de Benito, Daniel, Hall, Judith G., Sawatzky, Bonita, Bedard, Tanya, Sanchez, Victoria Castillo, Navalon‐Martinez, Carolina, Pan, Tony, Hilton, Coleman, Dahan‐Oliel, Noémi

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Opportunities for immunotherapy in microsatellite instable colorectal cancer von Westdorp, Harm, Fennemann, Felix L., Weren, Robbert D. A., Bisseling, Tanya M., Ligtenberg, Marjolijn J. L., Figdor, Carl G., Schreibelt, Gerty, Hoogerbrugge, Nicoline, Wimmers, Florian, de Vries, I. Jolanda M.

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Aberrant Cortical Activity in Multiple GCaMP6-Expressing Transgenic Mouse Lines von Steinmetz, Nicholas A, Buetfering, Christina, Lecoq, Jerome, Lee, Christian R, Peters, Andrew J, Jacobs, Elina A K, Coen, Philip, Ollerenshaw, Douglas R, Valley, Matthew T, de Vries, Saskia E J, Garrett, Marina, Zhuang, Jun, Groblewski, Peter A, Manavi, Sahar, Miles, Jesse, White, Casey, Lee, Eric, Griffin, Fiona, Larkin, Joshua D, Roll, Kate, Cross, Sissy, Nguyen, Thuyanh V, Larsen, Rachael, Pendergraft, Julie, Daigle, Tanya, Tasic, Bosiljka, Thompson, Carol L, Waters, Jack, Olsen, Shawn, Margolis, David J, Zeng, Hongkui, Hausser, Michael, Carandini, Matteo, Harris, Kenneth D

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Éléments de données communs pour l'arthrogrypose multiple congénitale: Un cadre international von Nematollahi, Shahrzad, Dieterich, Klaus, Filges, Isabel, De Vries, Johanna I P, Van Bosse, Harold, Natera-De Benito, Daniel, Hall, Judith G, Sawatzky, Bonita, Bedard, Tanya, Sanchez, Victoria Castillo, Navalon-Martinez, Carolina, Pan, Tony, Hilton, Coleman, Dahan-Oliel, Noémi

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Elementos de datos comunes para la artrogriposis múltiple congénita: Un marco internacional von Nematollahi, Shahrzad, Dieterich, Klaus, Filges, Isabel, De Vries, Johanna I P, Van Bosse, Harold, Natera de Benito, Daniel, Hall, Judith G, Sawatzky, Bonita, Bedard, Tanya, Sanchez, Victoria Castillo, Navalon-Martinez, Carolina, Pan, Tony, Hilton, Coleman, Dahan-Oliel, Noémi

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Prevalence and architecture of de novo mutations in developmental disorders von McRae, Jeremy F, Clayton, Stephen, Mason, Laura E, Tivey, Adrian R, Ahmed, Munaza, Awada, Jana, Balasubramanian, Meena, Banka, Siddharth, Bennett, Chris, Bernhard, Birgitta, Bevan, A. Paul, Blair, Edward, Blyth, Moira, Burn, John, Castle, Bruce, Clasper, Susan, Collins, Amanda, Collinson, Morag N, Dabir, Tabib, Davidson, Rosemarie, Davies, Sally, Dean, John, Donnai, Dian, Ellard, Sian, Ellis, Ian, Everest, Sarah, Foulds, Nicola, Fryer, Alan, Gaunt, Lorraine, Goudie, David, Gray, Emma, Greene, Philip, Gribble, Susan, Henderson, Alex, Hildyard, Lucy, Holden, Simon, Holder, Muriel, Ingram, Stuart, Jackson, Andrew, Kaemba, Beckie, Kazembe, Sandra, Kinning, Esther, Kraus, Alison, Kumar, V. K. Ajith, Lachlan, Katherine, Lam, Wayne, Lim, Derek, Longman, Cheryl, Lynch, Sally A, Maher, Eddy, Maye, Una, McKay, Kirsten, McWilliam, Catherine, Metcalfe, Kay, Morgan, Sian, Murday, Victoria, Murphy, Helen, Nemeth, Andrea, Nevitt, Louise, Newbury-Ecob, Ruth, Park, Soo-Mi, Paterson, Joan, Payne, Stewart, Perrett, Daniel, Pratt, Norman, Quarrell, Oliver, Randall, Josh, Rankin, Julia, Raymond, Lucy, Robert, Leema, Roberts, Paul, Saggar, Anand, Samant, Shalaka, Sampson, Julian, Sandford, Richard, Selby, Ann, Sequeira, Cheryl, Shearing, Emma, Smith, Audrey, Smith, Kath, Splitt, Miranda, Suri, Mohnish, Sutton, Vivienne, Tatton-Brown, Kate, Temple, I. Karen, Turner, Claire, Varghese, Vinod, Vasudevan, Pradeep, Vogt, Julie, Wakeling, Emma, Wilcox, Sarah, Williams, Denise, Williams, Nicola, Wilson, Louise, Wright, Michael, Yates, Laura, Yau, Michael, Wright, Caroline F, FitzPatrick, David R, Barrett, Jeffrey C

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A Bayesian Modeling Approach to Situated Design of Personalized Soundscaping Algorithms von van Erp, Bart, Podusenko, Albert, Ignatenko, Tanya, de Vries, Bert

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Effectiveness of family-based therapy for depressive symptoms in children and adolescents: A systematic review and meta-analysis von van Aswegen, Tanya, Samartzi, Eleonora, Morris, Linzette, van der Spek, Nadia, de Vries, Ralph, Seedat, Soraya, van Straten, Annemieke

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A blueprint for health technology assessment capacity building: lessons learned from Malta von Abraham, Katharina, Kvamme, Ingelin, Magrin Sammut, Sylvana, de Vries, Simone, Formosa, Tanya, Dupree, Rudy, Corro Ramos, Isaac, Goettsch, Wim, Franken, Margreet

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A blueprint for health technology assessment capacity building: lessons learned from Malta von Abraham, Katharina, Kvamme, Ingelin, Magrin Sammut, Sylvana, de Vries, Simone, Formosa, Tanya, Dupree, Rudy, Corro Ramos, Isaac, Goettsch, Wim, Franken, Margreet

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ESMO/ASCO recommendations for a Global Curriculum (GC) in medical oncology—edition 2016 von Dittrich, C., Kosty, M., Jezdic, S., Pyle, D., Berardi, R., Bergh, J., Lotz, J.-P., Österlund, P., Pavlidis, N., Purkalne, G., Carraway, Hetty, Lee Close, Julia, Gilbert, Jill, Bokemeyer, Carsten, Cervantes, Andrés, Ohe, Yuichiro, Pless, Miklos, McGregor, Keith, Fumassoli, Katharine, Candiani, Roberta, Bricalli, Gracemarie, Kenny, Tanya, Latino, Nicola, Cogo, Marina, Pavinato, Vanessa, Marchesi, Vanessa, Awada, Ahmad, Banerjee, Susana, Bhatia, Smita, Bogaerts, Jan, Buckner, Jan, Cardoso, Fatima, Casali, Paolo, Chu, Edward, Coiffier, Bertrand, Connolly, Roisin, Coupland, Sarah, De Petris, Luigi, De Santis, Maria, de Vries, Elisabeth G.E., Dizon, Don S., Duff, Jennifer, Duska, Linda R., Eniu, Alexandru, Ernstoff, Marc, Felip, Enriqueta, Fey, Martin F., Glaudemans, Andor W.J.M., Gopalan, Priya K., Grothey, Axel, Hahn, Stephen M., Hanna, Diana, Herold, Christian, Herrstedt, Jørn, Homicsko, Krisztian, Jones, Dennie V., Jost, Lorenz, Keilholz, Ulrich, Khan, Saad, Kiss, Alexander, Köhne, Claus-Henning, Kunstfeld, Rainer, Lichtman, Stuart, Licitra, Lisa, Lion, Thomas, Litière, Saskia, Loehrer, Patrick J., Jennifer Markham, Merry, Markman, Ben, Mayerhoefer, Marius, Meran, Johannes G., Michielin, Olivier, Charlotte Moser, Elizabeth, Mountzios, Giannis, Moynihan, Timothy, Palumbo, Antonio, Alessandro Peccatori, Fedro, Pfeilstöcker, Michael, Raut, Chandrajit, Remick, Scot C., Rutkowski, Piotr, Salgado, Roberto, Schernhammer, Eva, Schlumberger, Martin, Schmoll, Hans-Joachim, Schnipper, Lowell, Sessa, Cristiana, Shapiro, Charles L., Steele, Julie, Sternberg, Cora N., Stiefel, Friedrich, Sullivan, Richard, Tabernero, Josep, Travado, Luzia, Verheij, Marcel, Voest, Emile, Von Roenn, Jamie, Weber, Jeffrey S., Wildiers, Hans, Yarden, Yosef

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Éléments de données communs pour l'arthrogrypose multiple congénitale: Un cadre international von Nematollahi, Shahrzad, Dieterich, Klaus, Filges, Isabel, De Vries, Johanna I. P., Van Bosse, Harold, Natera‐De Benito, Daniel, Hall, Judith G., Sawatzky, Bonita, Bedard, Tanya, Sanchez, Victoria Castillo, Navalon‐Martinez, Carolina, Pan, Tony, Hilton, Coleman, Dahan‐Oliel, Noémi

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Elementos de datos comunes para la artrogriposis múltiple congénita: Un marco internacional von Nematollahi, Shahrzad, Dieterich, Klaus, Filges, Isabel, De Vries, Johanna I. P., Van Bosse, Harold, Natera de Benito, Daniel, Hall, Judith G., Sawatzky, Bonita, Bedard, Tanya, Sanchez, Victoria Castillo, Navalon‐Martinez, Carolina, Pan, Tony, Hilton, Coleman, Dahan‐Oliel, Noémi

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Blok, Lot Snijders, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls von Mercader, Josep M., Udler, Miriam S., Mahajan, Anubha, Caulkins, Lizz, Barajas-Olmos, Francisco, Blackwell, Thomas W., Boerwinkle, Eric, Brody, Jennifer A., Chen, Siying, Contreras-Cubas, Cecilia, Córdova, Emilio, Correa, Adolfo, Cortes, Maria, Dolan, Lawrence, Drews, Kimberly L., Gabriel, Stacey, Garay-Sevilla, Maria Eugenia, García-Ortiz, Humberto, Gross, Myron, Heard-Costa, Nancy L., Jackson, Anne U., Jørgensen, Marit E., Kang, Hyun Min, Kim, Bong-Jo, Lyssenko, Valeriya, Manning, Alisa K., Marcketta, Anthony, Martínez-Hernández, Angélica, Matsuo, Karen, Mayer-Davis, Elizabeth, Mohlke, Karen L., Morrison, Alanna C., Ndungu, Anne, Ng, Maggie C. Y., O’Dushlaine, Colm, Payne, Anthony J., Pihoker, Catherine, Preuss, Michael, Psaty, Bruce M., Reiner, Alexander P., Robertson, Neil R., Santoro, Nicola, Schurmann, Claudia, So, Wing Yee, Soberón, Xavier, Thameem, Farook, Tomlinson, Brian, van Dam, Rob M., Vujkovic, Marijana, Witte, Daniel R., Barzilai, Nir, Bonnycastle, Lori L., Bowden, Donald W., Chambers, John C., Cheng, Ching-Yu, de Vries, Paul S., Glaser, Benjamin, Groop, Leif, Kooner, Jaspal Singh, Kwak, Soo Heon, Lehman, Donna M., Spector, Timothy D., Tai, E. Shyong, Tuomilehto, Jaakko, Wilson, James G., Burke, Brian, Carey, David J., Chan, Juliana C. N., Dupuis, Josée, Frossard, Philippe, Heckbert, Susan R., Hwang, Mi Yeong, Kim, Young Jin, Kirchner, H. Lester, Lee, Jong-Young, Lee, Juyoung, Loos, Ruth J. F., Ma, Ronald C. W., O’Donnell, Christopher J., Park, Kyong Soo, Rasheed, Asif, Saleheen, Danish, Sim, Xueling, Hanis, Craig L., Orozco, Lorena, Dewey, Frederick E., Baras, Aris, Gieger, Christian, Meitinger, Thomas, Strauch, Konstantin, Lange, Leslie, Hansen, Torben, Pedersen, Oluf, Dabelea, Dana, Bell, Graeme I., Sladek, Rob, Rich, Steve S., Rotter, Jerome I., Altshuler, David, Boehnke, Michael

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FITTING AGENT WITH USER MODEL INITIALIZATION FOR A HEARING DEVICE von Ignatenko, Tanya, Kondrashov, Kirill, de Vries, Bert

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Fitting agent for a hearing device and method for updating a multi-environment user model von Ignatenko, Tanya, Kondrashov, Kirill, De Vries, Aalbert

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On Preference Learning Based on Sequential Bayesian Optimization with Pairwise Comparison von Ignatenko, Tanya, Kondrashov, Kirill, Cox, Marco, de Vries, Bert

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