Treffer 1 - 20 von 25 für Suche 'Sampson, Evan E.', Suchdauer: 1,69s Treffer weiter einschränken
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    Development of a Definition of Postacute Sequelae of SARS-CoV-2 Infection von Thaweethai, Tanayott, Jolley, Sarah E, Karlson, Elizabeth W, Levy, Bruce, McCorkell, Lisa, Parthasarathy, Sairam, Singh, Upinder, Schulte, Carolin C. M, Atchley-Challenner, Rachel, Horwitz, Leora I, Alba, George A, Alicic, Radica, Anglin, Khamal, Argueta, Urania, Ashktorab, Hassan, Baslet, Gaston, Bateman, Lucinda, Bhattacharyya, Shamik, Blomkalns, Andra L, Brim, Hassan, Chan, James, Charney, Alexander W, Cribbs, Sushma K, Deeks, Steven G, Farah-Abraham, Rachael, Feuerriegel, Elen M, Fonseca, Vivian, Franko, Nicholas, Gainer, Vivian, Gander, Jennifer C, Geng, Linda N, Go, Minjoung, Goldman, Jason D, Grebe, Halle, Hafner, John, Hanson, Keith A, Hernandez, Carla, Hess, Rachel, Hodder, Sally L, Huang, Beatrice, John, Janice, Jordan, Michael R, Katz, Stuart D, Kelly, Sara W, Kirwan, John P, Klein, Jonathan D, Knox, Kenneth S, Krishnan, Jerry A, Kumar, Andre, Lanca, Margaret, Logarbo, Brian P, Longo, Michele T, Luciano, Carlos A, Maley, Jason H, Mallett, Gail, Marathe, Jai G, Marconi, Vincent, Marshall, Gailen D, Mendez-Figueroa, Hector, Metz, Torri D, Morse, Richard, Mosier, Jarrod, Murphy, Shawn N, Neuman, Robert B, Ofotokun, Ighovwerha, Ojemakinde, Elizabeth, Palomares, Kristy, Patterson, Jan E, Pemu, Priscilla, Pogreba-Brown, Kristen, Poppas, Athena, Quigley, John G, Reece, Rebecca, Reeder, Harrison, Reeves, W. B, Reiman, Eric M, Rischard, Franz, Rosand, Jonathan, Rouse, Dwight J, Ruff, Adam, Saade, George, Sandoval, Grecio J, Santana, Jorge L, Schlater, Shannon M, Skupski, Daniel W, Sparks, Jeffrey A, Taylor, Barbara S, Thuluvath, Paul, Ticotsky, Amberly, Urdaneta, Alfredo E, Valdivieso, Daisy, Vasey, Andrew, Verduzco-Gutierrez, Monica, Ward, Honorine D, Warren, David E, Whiteheart, Sidney W, Wiley, Zanthia, Wisnivesky, Juan P, Yee, Lynn M, Zisis, Sokratis


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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

    Veröffentlicht in Nature (London)

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    Phase 3, Randomized, 20-Month Study of Bimatoprost Implant in Open-Angle Glaucoma and Ocular Hypertension (ARTEMIS 1) von Medeiros, Felipe A., Kolko, Miriam, Bejanian, Marina, Goodkin, Margot L., Guo, Qiang, Robinson, Michael R., Agar, Ashish, Coote, Michael, Bathijia, Renuka, Liu, Lance, Roberts, Tim, Faschinger, Christoph, Collignon, Nathalie, Alves Pereira, Ana Claudia, Dantas, Fernando Justino, Lopes da Silva, Marcelo Jordao, Kanadani, Fabio, Prata, Tiago, Bach-Holm, Daniella, Kolko, Miriam, Lai, Jimmy, Tham, Clement, Bátor, György, Szalczer, Lajos, Varsányi, Balázs, Blumenthal, Eytan, Geyer, Orna, Lavartovsky, Shmuel, Pedut-Kloizman, Tamar, Shoham-Hazon, Nir, Lujan, Silvio, Abela, Benjamin, Ang, Robert E., Leuenberger, Edgar U., Uy, Harvey, Yap-Veloso, Maria Imelda, Fryczkowski, Piotr, Jurowski, Piotr, Kalużny, Bartlomiej, Raczynska, Krystyna, Tomczyk-Dorozynska, Wioletta, Wasyluk, Jaromir, Zalewski, Slawomir, Feijoó, Julian Garcia, Giménez-Gómez, Rafael, Griño, Elena Milla, López, Alfonso Antón, Miralles, Merce Guarro, Moreno, Javier Montero, Taulet, Enrique Cervera, Zúñiga, Beatriz Ponte, Chen, Ying-Ying, Lee, Yuan-Chieh, Alpern, Louis, Berlin, Michael S., Brubaker, Jacob, Caldwell, Delmar, Camp, Andrew, Cantor, Louis B., Caronia, Ronald, Crane, Charles J., Day, Douglas, Duzman, Eran, Elfervig, John, Evans, Richard, Flynn, William John, Foster, Charles Stephen, Frenkel, Ronald, Goyal, Raj, Hartman, Paul J., Haynes, William L., Jerkins, Gary, Kim, Janet, Kwapiszeski, Bradley, Larsen, Christine, Levenson, Jeffrey H., Logan, Dwayne, McMillan, Brian, Martel, Joseph R., Moroi, Sayoko, Moyes, Andrew, Myers, Jonathan, Nairn, John, Nielsen, Steven, Paauw, James, Pai, Vicky, Park, Abraham, Qazi, Mujtaba A., Rhee, Douglas J., Sampson, Reginald, Shrivastava, Anurag, Simmons, Steven T., Sims, Annette, Slabaugh, Mark A., Smetana, Scott, Smith, Oluwatosin, So, Scott C., Wallshein, Jay, Walters, Thomas R., Zaman, Fiaz


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    Estimating treatment coverage for people with substance use disorders: an analysis of data from the World Mental Health Surveys von Glantz, Meyer, Thornicroft, Graham, Al‐Hamzawi, Ali, Alonso, Jordi, Bruffaerts, Ronny, Bunting, Brendan, Bromet, Evelyn J., Miguel Caldas de Almeida, José, Florescu, Silvia, Gureje, Oye, Maria Haro, Josep, Karam, Aimee, Karam, Elie G., Levinson, Daphna, Elena Medina‐Mora, Maria, Nakamura, Yosikazu, Navarro‐Mateu, Fernando, Pennell, Beth‐Ellen, Posada‐Villa, José, Stein, Dan J., ten Have, Margreet, Chatterji, Somnath, Adamowski, Tomasz, Aguilar‐Gaxiola, Sergio, Al‐Hamzawi, Ali, Al‐Kaisy, Mohammad, Alonso, Jordi, Altwaijri, Yasmin, Andrade, Laura Helena, Atwoli, Lukoye, Auerbach, Randy P., Axinn, William G., Benjet, Corina, Borges, Guilherme, Bromet, Evelyn J., Bruffaerts, Ronny, Bunting, Brendan, Caldas de Almeida, José Miguel, Cardoso, Graça, Chardoul, Stephanie, Chatterji, Somnath, Filho, Alexandre Chiavegatto, Cia, Alfredo H., Cuijpers, Pim, Degenhardt, Louisa, de Girolamo, Giovanni, de Graaf, Ron, de Jonge, Peter, Ebert, David D., Evans‐Lacko, Sara, Fayyad, John, Florescu, Silvia, Galea, Sandro, Ghimire, Dirgha J., Gilman, Stephen E., Glantz, Meyer D., Gluzman, Semyon, Gureje, Oye, Haro, Josep Maria, Harris, Meredith G., He, Yanling, Hinkov, Hristo, Hu, Chi‐Yi, Huang, Yueqin, Karam, Elie G., Kawakami, Norito, Kiejna, Andrzej, Koenen, Karestan C., Kovess‐Masfety, Viviane, Lara, Carmen, Lee, Sing, Lepine, Jean‐Pierre, Levav, Itzhak, Levinson, Daphna, Liu, Zhaorui, Martins, Silvia S., McLaughlin, Katie A., Medina‐Mora, Maria Elena, Mneimneh, Zeina, Moskalewicz, Jacek, Navarro‐Mateu, Fernando, Nock, Matthew K., O'Neill, Siobhan, Ormel, Johan, Posada‐Villa, José, Ruscio, Ayelet M., Slade, Tim, Smoller, Jordan W., Stein, Dan J., Street, Amy E., Tachimori, Hisateru, Thornicroft, Graham, Torres, Yolanda, Vilagut, Gemma, Viana, Maria Carmen, Wells, Elisabeth, Williams, David R., Williams, Michelle A., Wojtyniak, Bogdan, Zaslavsky, Alan M.

    Veröffentlicht in World psychiatry

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    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.

    Veröffentlicht in Nature communications

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    Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia von 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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    Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy von Abou Jamra, Rami, Accogli, Andrea, Amburgey, Kimberly, Basinger, Alice A., Ceulemans, Sophia, Charles, Perrine, McRae, Jeremy F., Rajan, Diana, Ambridge, Kirsty, Jones, Philip, Jones, Wendy D., Ahmed, Munaza, Anjum, Uruj, Armstrong, Ruth, Barnicoat, Angela, Bennett, Chris, Blair, Edward, Blyth, Moira, Bourdon, Louise, Brady, Angela, Burn, John, Canham, Natalie, Cilliers, Deirdre, Clayton-Smith, Jill, Coates, Andrea, Cooper, Nicola, Dabir, Tabib, Davies, Sally, Dean, John, Devlin, Gemma, Donnai, Dian, Donnelly, Carina, Evans, Karenza, Fendick, Tina, Goodship, Judith, Green, Andrew, Harrison, Lucy, Holden, Simon, Jarvis, Joanna, Johnson, Diana, Jones, Elizabeth, Kumar, V. K. Ajith, Lachlan, Katherine, Langman, Caroline, Maye, Una, McMullan, Dominic J., McWilliam, Catherine, Metcalfe, Kay, Norman, Andrew, Ogilvie, Caroline, Park, Soo-Mi, Phipps, Julie, Prescott, Katrina, Procter, Annie, Purnell, Hellen, Ross, Alison, Sampson, Julian, Shannon, Nora, Skitt, Zara, Stewart, Fiona, Stewart, Helen, Swaminathan, Ganesh Jawahar, Taylor, Cat, Tein, Mark, Treacy, Becky, Vandersteen, Anthony, Wallwark, Sarah, Waters, Jonathon, Weber, Astrid, Whiteford, Margo, Widaa, Sara, Wilcox, Sarah, Wilkinson, Emily, Parker, Michael, FitzPatrick, David R., Demurger, Florence, Eiset, Saga Elise, Ferrarini, Alessandra, Haack, Tobias B., Hashim, Mona, Jonasson, Amy R., Kok, Fernando, Marcelis, Carlo L.M., McWalter, Kirsty, Mercimek-Andrews, Saadet, Person, Richard, Ramelli, Gian Paolo, Rauch, Anita, Sanchez-Valle, Amarilis, Sattar, Shifteh, Saunders, Carol, Steindl, Katharina, Syrbe, Steffen, Taylor, Jenny C., Trauner, Doris A., Vogel, Ida, Widjaja, Elysa, Zak, Jaroslav, Banka, Siddharth, Rodan, Lance H.


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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.

    Veröffentlicht in Nature communications

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