Treffer 1 - 20 von 36 für Suche 'HIGH ANGELA D', Suchdauer: 1,47s Treffer weiter einschränken
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    Clinical features and management of individuals admitted to hospital with monkeypox and associated complications across the UK: a retrospective cohort study von Callaby, Helen, Luintel, Akish, Beynon, William, Bond, Helena, O'Hara, Geraldine, Peters, Joanna R, Payne, Lara, Mody, Nisha, Rampling, Tommy, Dunning, Jake, Milligan, Iain D, Lamb, Lucy E, Moores, Rachel C, Irish, Dianne, Jalal, Hamid, Mack, Damien, Miller, Robert, Gil, Eliza, Spicer, Wendy, Furneaux, Jenna, Matthew, Jones, Matthew, Hannah J, Vipond, Richard, Gibney, Barry, Hunter, Michael, McCarty, Emma, Li, Kathy, McGinnity, Katherine, Culbert, Carly, Jeong, Eunjin, Dyche, Jessica, McCormick, Hannah, Heskin, Joseph, Walters, Yasmin, Tung, Hsiu, Patel, Kinjal, Henderson, Merle, Peres, Edu, Dickinson, Molly, Mughal, Nabeela, Hughes, Stephen, Chitlangia, Shrada, Heaslip, Vivian, Girometti, Nicolo, Pond, Marcus, Naidu, Vasanth V, Brown, Aisling, Goodman, Anna, Newsholme, William, Bilinska, Julia, SA Pinto, Pedro, Haque, Sarah, Gideon, Tseday, Jerome-oboh, Damilola, Rimmer, Stephanie, Dosekun, Olamide, Davies, Ella, Taylor, Lauren, Alagratnam, Jasmini, Payne, Lara V S, Nic Fhogartaigh, Caoimhe, Bholah, Salmaan, Lampejo, Temi, Middleditch, Holly, Mulka, Larissa, Downey, Michael R, McCallum, Craig I, Ratcliffe, Libuse, Gould, Susie, Cruise, James, Keating, Grace, Harrison, Daniel, Willoughby, Shay, Jarvis, Anthony, Smielewska, Anna, Foley, Fiona, Friday, Dawn, Joseph, Deepa, Salinas, Jason, Ume, Uchenna, Wallis, Gabriel, Johnson, Leann, Ustianowski, Andrew, Dancso, Balazs, Ghosh, Samit, Goodwin, Lynsey, Murray, Charlotte, Salthouse, Kirstie, Mulligan, Robert, Brolly, Jacob, Nwajiugo, Paul, Schmid, Matthias, Schwab, Uli, Payne, Brendan, Karageorgopoulos, Drosos E, Dagens, Andrew B, Farrow, Sam, Bicanic, Tihana, Riordan, Andrew, Whittaker, Elizabeth

    Veröffentlicht in The Lancet infectious diseases

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    Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate–binding region von Kelly, McKenna, Park, Meredith, Mihalek, Ivana, Pérez‐Palma, Eduardo, Anselm, Irina, Briere, Lauren C., High, Frances A., Sweetser, David A., Allard, Patrick, Ashley, Euan A., Bacino, Carlos A., Baker, Eva, Barseghyan, Hayk, Batzli, Gabriel F., Behnam, Babak, Bellen, Hugo J., Bernstein, Jonathan A., Bican, Anna, Bostwick, Bret L., Brush, Matthew, Burke, Elizabeth A., Burrage, Lindsay C., Butte, Manish J., Clark, Gary D., Colley, Heather A., Cooper, Cynthia M., Davids, Mariska, Dell’Angelica, Esteban C., Dorrani, Naghmeh, Douine, Emilie D., Emrick, Lisa T., Fairbrother, Laura, Fernandez, Liliana, Ferreira, Carlos, Fieg, Elizabeth L., Fisher, Paul G., Friedman, Noah D., Gahl, William A., Gourdine, Jean‐Philippe F., Groden, Catherine A., Gropman, Andrea L., Haendel, Melissa, Hom, Jason, Howerton, Ellen M., Jamal, Fariha, Jiang, Yong‐hui, Johnston, Jean M., Jones, Angela L., Karaviti, Lefkothea, Koeller, David M., Kohane, Isaac S., Koziura, Mary, Lalani, Seema R., Lazar, Jozef, Levy, Shawn E., Lincoln, Sharyn A., Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Maduro, Valerie V., Majcherska, Marta M., Malicdan, May Christine V., Mamounas, Laura A., Manolio, Teri A., Markello, Thomas C., Marom, Ronit, Martínez‐Agosto, Julian A., May, Thomas, Morimoto, Marie, Mulvihill, John J., Murphy, Jennifer L., Nelson, Stan F., Newman, John H., Novacic, Donna, Orange, Jordan S., Potocki, Lorraine, Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Sampson, Jacinda B., Samson, Susan L., Schoch, Kelly, Silverman, Edwin K., Sinsheimer, Janet S., Smith, Kevin S., Spillmann, Rebecca C., Stong, Nicholas, Sullivan, Jennifer A., Waggott, Daryl M., Walsh, Chris A., Wangler, Michael F., Ward, Patricia A., Waters, Katrina M., Westerfield, Monte, Wheeler, Matthew T., Wise, Anastasia L., Worthey, Elizabeth A., Yoon, Amanda J., Zastrow, Diane B.

    Veröffentlicht in Epilepsia (Copenhagen)

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    Genomic and Molecular Analyses Identify Molecular Subtypes of Pancreatic Cancer Recurrence von Dreyer, Stephan B., Upstill-Goddard, Rosie, Legrini, Assya, Biankin, Andrew V., Allison, Sarah, Biankin, Andrew V., Beraldi, Dario, Cameron, Euan, Cunningham, Richard, Dreyer, Stephan, Grimwood, Paul, Kelly, Shane, Marshall, John, McDade, Brian, Musgrove, Elizabeth A., Ramsay, Donna, Upstill-Goddard, Rosie, Rebus, Selma, Rahib, Lola, Serrels, Bryan, Jamieson, Nigel B., McKay, Colin J., Westwood, Paul, Williams, Nicola, Duthie, Fraser, Shen, William, Pea, Antonio, Johns, Amber L., Gill, Anthony J., Timpson, Paul, Chou, Angela, Pajic, Marina, Dwarte, Tanya, Herrmann, David, Vennin, Claire, Cox, Thomas R., Pereira, Brooke, Ritchiee, Shona, Reed, Daniel A., Chambers, Cecilia R., Metcalf, Xanthe, Nobis, Max, Jeong, Gloria, Kenyon, Lara, Lyons, Ruth J., Waddell, Nicola, Pearson, John V., Patch, Ann-Marie, Newell, Felicity, Addala, Venkateswar, Kazakoff, Stephen, Holmes, Oliver, Leonard, Conrad, Grimmond, Sean M., Hofmann, Oliver, Samra, Jaswinder S., Pavlakis, Nick, Arena, Jennifer, High, Hilda A., Asghari, Ray, Merrett, Neil D., Cosman, Peter H., Williams, David, Spigellman, Allan, McLeod, Duncan, Kirk, Judy, Kench, James G., Sandroussi, Charbel, Goodwin, Annabel, Andrews, Lesley, Texler, Michael, Forrest, Cindy, Ballal, Mo, Fletcher, David, Beilin, Maria, Feeney, Kynan, Epari, Krishna, Zeps, Nikolajs, Nguyen, Nan Q., Ruszkiewicz, Andrew R., Worthley, Chris, Brooke-Smith, Mark E., Papangelis, Virginia, Clouston, Andrew D., Barbour, Andrew P., O’Rourke, Thomas J., Fawcett, Jonathan W., Hatzifotis, Michael, Nikfarjam, Mehrdad, Eshleman, James R., Hruban, Ralph H., Wolfgang, Christopher L., Scarpa, Aldo, Biankin, Andrew V., Jamieson, Nigel B., Chang, David K., Jamieson, Nigel B., Chang, David K., Jamieson, Nigel B., Chang, David K.


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    Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder von Ugur, Berrak, Zhang, Bo, Feng, Wenjia, Goddard, Pagé, Kravets, Elijah, Marwaha, Shruti, Adams, David R., Andrews, Ashley, Behrens, Edward, Berg-Rood, Beverly, Berry, Gerard T., Bohnsack, John, Botto, Lorenzo, Boyd, Brenna, Briere, Lauren C., Carrasquillo, Olveen, Chanprasert, Sirisak, Chinn, Ivan, Coggins, Matthew, Sessions Cole, F., Cope, Heidi, Dasari, Surendra, Dayal, Jyoti G., Dipple, Katrina, Doherty, Daniel, Dorrani, Naghmeh, Doss, Argenia L., Earl, Dawn, Ezell, Kimberly, Fisher, Paul G., Gahl, William A., Glass, Ian, Goddard, Page C., Halley, Meghan C., High, Frances, Hisama, Fuki M., Holm, Ingrid A., Hutchison, Sarah, Isasi, Rosario, Izumi, Kosuke, Jarvik, Gail P., Ketkar, Shamika, Kohane, Isaac S., Kohler, Jennefer N., Kozuira, Mary, Lalani, Seema R., Lam, Byron, Lam, Christina, Lanpher, Brendan C., Levitt, Roy, Lewis, Richard A., Liu, Pengfei, Liu, Xue Zhong, Longo, Nicola, Maas, Richard L., Manolio, Teri A., Mao, Rong, Marom, Ronit, Martin, Beth A., Marwaha, Shruti, McCauley, Jacob, McCray, Alexa T., Mefford, Heather, Morava, Eva, Moretti, Paolo, Nakano-Okuno, Mariko, Nelson, Stanley F., Neumann, Serena, Nickerson, Deborah, Palmer, Christina G.S., Parker, Neil H., Phillips, John A., Pusey Swerdzewski, Barbara N., Renteria, Genecee, Rosenfeld, Jill A., Sacco, Ralph, Schoch, Kelly, Shin, Jimann, Silverman, Edwin K., Sisco, Kathy, Smith, Edward C., Solomon, Ben, Sweetser, David A., Tran, Alyssa A., Velinder, Matt, Walley, Nicole M., Wambach, Jennifer, Wan, Jijun, Ward, Patricia A., Wegner, Daniel, Hubshman, Monika Weisz, Wener, Mark, Wenger, Tara, Worley, Kim, Xiao, Changrui, Yang, John, Zuchner, Stephan, Worthey, Elizabeth A., Postlethwait, John, Solnica-Krezel, Lila

    Veröffentlicht in Genetics in medicine

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    An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids von Ruiter, Jos P.N., van Lint, Alida E.M., Pras-Raves, Mia, Wever, Eric, Guillen Sacoto, Maria J., Begtrup, Amber, Tarnopolsky, Mark, Sell, Susan L., Nowak, Catherine B., Douglas, Jessica, Perlman, Seth, Martin, Nicole, Brault, Jennifer, Gahl, William A., Alejandro, Mercedes E., Dai, Hongzheng, Dhar, Shweta U., Hanchard, Neil A., Lee, Brendan H., Moretti, Paolo M., Murdock, David R., Nicholas, Sarah K., Potocki, Lorraine, Scott, Daryl A., Eng, Christine M., Deardorff, Matthew, Hassey, Kelly, Sullivan, Kathleen, Tan, Queenie K.-G., Beggs, Alan H., Berry, Gerard T., Cooper, Cynthia M., Pallais, J. Carl, Rodan, Lance H., Kelley, Emily G., Morava, Eva, Forghani, Irman, Lam, Byron, Levitt, Roy, Liu, Xue Zhong, McCauley, Jacob, Tekin, Mustafa, Thorson, Willa, Findley, Laurie C., Krasnewich, Donna M., Manolio, Teri A., Goldrich, Madison P., Draper, David D., Nath, Avi, Pusey, Barbara N., Toro, Camilo, Baker, Eva, Gochuico, Bernadette, Mosbrook-Davis, Deborah, Rossignol, Francis, Adam, Margaret, Amendola, Laura, Cunningham, Michael, Jarvik, Gail P., Jarvik, Jeffrey, Lam, Christina, Raskind, Wendy, Sybert, Virginia, Ashley, Euan A., Coakley, Terra R., Hom, Jason, Majcherska, Marta M., Martin, Beth A., Marwaha, Shruti, Ruzhnikov, Maura, Tabor, Holly K., Tucker, Brianna M., Zastrow, Diane B., Byrd, William E., Dell’Angelica, Esteban C., Douine, Emilie D., Mak, Bryan C., Martin, Martin G., Martínez-Agosto, Julian A., McGee, Elisabeth, Nelson, Stanley F., Parker, Neil H., Sinsheimer, Janet S., Wang, Lee-kai, Perry, Katherine Wesseling, Woods, Jeremy D., Pace, Laura, Marth, Gabor, Viskochil, Dave, Bayrak-Toydemir, Pinar, Duncan, Laura, Robertson, Amy K., Solem, Emily, Schedl, Timothy, Shin, Jimann, Solnica-Krezel, Lilianna, Waisfisz, Quinten, Zwijnenburg, Petra J.G., Wanders, Ronald J.A., Vaz, Frédéric M.

    Veröffentlicht in Genetics in medicine

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    BOugie or stylet in patients UnderGoing Intubation Emergently (BOUGIE): protocol and statistical analysis plan for a randomised clinical trial von Driver, Brian, Semler, Matthew W, Self, Wesley H, Ginde, Adit A, Gandotra, Sheetal, Trent, Stacy A, Smith, Lane M, Gaillard, John P, Page, David B, Whitson, Micah R, Vonderhaar, Derek J, Joffe, AM, West, Jason R, Hughes, Christopher, Landsperger, Janna S, Howell, Michelle P, Russell, Derek W, Gulati, Swati, Bentov, Itay, Mitchell, Steven, Latimer, Andrew, Doerschug, Kevin, Koppurapu, Vikas, Gibbs, Kevin W, Wang, Li, Lindsell, Christopher John, Janz, David, Rice, Todd W, Prekker, Matthew E, Casey, Jonathan D, Barnes, Christopher, Cupelo, Alicia K, DeVries, Paige, Dye, Sally, Fletcher, Andrea, Gray, Christopher S, High, Kevin, Kurz, Michael C, Lyle, Carol L, Mitchell, Robert, Oeth, Justin, Rice, Erika LW, Robison, Sarah W, Schick, Alexandra, Stang, Jamie, Walters, Andrew M, Westphal, Nathaniel D, Watase, Tak, Lloyd, Bradley, Krishnamoorthy, Vijay, Bartz, Raquel R, Fox, William C, Whittle, John, Alvis, Bret D, Demasi, Stephanie C, Goyack, Laura E, Ford, Kristy K, Mattox, Trevor S, Altz-Stamm, Anna, Bardita, Cristina, Boone, Mary Clay, Chiles, Joe W, Collins, Kristina, Drescher, Abby, Dsouza, Kevin G, Dunn, Janna, Ejem, Stacy, Gautney, Josh, Harris, Nicole, Herder, Savannah, Hudali, Tamer, Chad Wade, R, Joshi, Rutwij, Kelmenson, Daniel, Mason, Anne Merrill, Merriman, Scott R, Mkorombindo, Takudzwa, Moore, Megan, Nowak, Jada, O’Connor, Kate, Patel, Sheylan D, Bruno Pereira, G, Sarratt, Lisa, Stewart, Tabitha, Stigler, William S, Vijaykumar, Kadambari, White, Gina, Defebio, Anthony, Friedel, Jennifer, Mohamed, Feysel, Nava, Karina, Otoo, Angela, Perez, Christian, Withers, Cori

    Veröffentlicht in BMJ open

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