Physical Activity Assessment and Promotion in Clinical Settings in the United States: A Scoping Review von Grogg, Kristin A., Giacobbi, Peter R., Blair, Emma K., Haggerty, Treah S., Lilly, Christa L., Winters, Carena S., Kelley, George A.

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ERp57 is protective against mutant SOD1-induced cellular pathology in amyotrophic lateral sclerosis von Parakh, Sonam, Jagaraj, Cyril J, Vidal, Marta, Ragagnin, Audrey M G, Perri, Emma R, Konopka, Anna, Toth, Reka P, Galper, Jasmin, Blair, Ian P, Thomas, Colleen J, Walker, Adam K, Yang, Shu, Spencer, Damian M, Atkin, Julie D

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Skin‐to‐skin contact after birth: Developing a research and practice guideline von Brimdyr, Kajsa, Stevens, Jeni, Svensson, Kristin, Blair, Anna, Turner‐Maffei, Cindy, Grady, Julie, Bastarache, Louise, Alfy, Abla, Crenshaw, Jeannette T., Giugliani, Elsa Regina Justo, Ewald, Uwe, Haider, Rukhsana, Jonas, Wibke, Kagawa, Mike, Lilliesköld, Siri, Maastrup, Ragnhild, Sinclair, Ravae, Swift, Emma, Takahashi, Yuki, Cadwell, Karin

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Impaired NHEJ repair in amyotrophic lateral sclerosis is associated with TDP-43 mutations von Konopka, Anna, Whelan, Donna R., Jamali, Md Shafi, Perri, Emma, Shahheydari, Hamideh, Toth, Reka P., Parakh, Sonam, Robinson, Tina, Cheong, Alison, Mehta, Prachi, Vidal, Marta, Ragagnin, Audrey M. G., Khizhnyak, Ivan, Jagaraj, Cyril J., Galper, Jasmin, Grima, Natalie, Deva, Anand, Shadfar, Sina, Nicholson, Garth A., Yang, Shu, Cutts, Suzanne M., Horejsi, Zuzana, Bell, Toby D. M., Walker, Adam K., Blair, Ian P., Atkin, Julie D.

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The Impact of Time of Day on Energy Expenditure: Implications for Long-Term Energy Balance von Shaw, Emma, Leung, Gloria K W, Jong, Jessica, Coates, Alison M, Davis, Rochelle, Blair, Merran, Huggins, Catherine E, Dorrian, Jillian, Banks, Siobhan, Kellow, Nicole J, Bonham, Maxine P

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Effects of fluoxetine on functional outcomes after acute stroke (FOCUS): a pragmatic, double-blind, randomised, controlled trial von Perry, David, Dinsmore, Lynn, Kambafwile, Mary, Idrovo, Luis, Hurley, Lisa, Kerwood, Lauriane, Merritt, Carley, Duty, Suzanna, Lindert, Ralf, Meegada, Madana, Maguire, Holly, Hiden, Joanne, Brodie, Fiona, Barcroft, Heather, Wightman, John, O Neill, Mark, Siddiqui, Amber, Rashmi, Sindhu, Wilson, Laura, Cullen, Claire, Keeling, Alison, Hindle, Julia, Maguire, Stuart, Hamid, Umair, Gaba, Waqar, Mohammed, Niaz, Robinson, Rianne, Mathieson, Philip, Jones, Val, Lush, Audrey, Bell, Jo, Badiani, Bhavna, Guo, Fenglin, Chamberlain, Angela, Donaldson, Dave, Melikyan, Elina, Oconnell, Susan, Hurdowar, Steve, Johnson, Matthew, Moore, Kimberley, Stevens, Angela, Burnip, Rachel, Beranova, Eva, Walker, Susannah, Cain, Rebecca, Willmot, Mark, Bates, Michelle, Pitt Ford, Alexandra, Aubrey, Beth, Howard, Joanne, Dhar, Saikat, Howard-Brown, Jennifer, Imam, Javed, Whitworth, Simon, Mcgee, Joanne, Hannon, Niamh, Mokoena, Langanani, Smart, Amanda, Donaldson, Fiona, Graham, Libby, Rowe, Joy, Munuswamy Vaiyapuri, Elangovan, Thomas, Lisa, Sharon, Storton, Jones, Paul, Johnston, Stuart, Pusalkar, Aparna, Broughton, David, Tryambake, Dinesh, Skotnicka, Agnieszka, Thompson, Jane, Annamalai, Arunkumar, Wilkinson, Peter, Young, Emma, Pereira, Rita, Drummond, Graham, Austin, Duncan, Funnell, Sarah, Jones, Stephanie, Vassallo, Joseph, Leonard, Dee, Wynter, Inez, Janbieh, Joumana, Wade, Lynne, Otter, Linda, Fleming, Amy, Jones, Rhian, Williams, Richard, Mavinamane, Sunanda, Hunt, Lorraine, Haque, Kashif, Gibson, Elspeth, Neves-Silva, Yara, Thompson, Alastair, Ritchings, Andrew, Mcredmond, Catherine, Goulding, Alicia, Punnoose, Sunil, Gordon, Laura, Tarkas, Tillana

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Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways von Cirulli, Elizabeth T., Lasseigne, Brittany N., Petrovski, Slavé, Sapp, Peter C., Dion, Patrick A., Leblond, Claire S., Couthouis, Julien, Lu, Yi-Fan, Wang, Quanli, Krueger, Brian J., Ren, Zhong, Keebler, Jonathan, Han, Yujun, Levy, Shawn E., Boone, Braden E., Wimbish, Jack R., Waite, Lindsay L., Jones, Angela L., Carulli, John P., Day-Williams, Aaron G., Staropoli, John F., Xin, Winnie W., Chesi, Alessandra, Raphael, Alya R., McKenna-Yasek, Diane, Cady, Janet, de Jong, J. M. B. Vianney, Kenna, Kevin P., Smith, Bradley N., Topp, Simon, Miller, Jack, Gkazi, Athina, Al-Chalabi, Ammar, van den Berg, Leonard H., Veldink, Jan, Silani, Vincenzo, Ticozzi, Nicola, Shaw, Christopher E., Baloh, Robert H., Appel, Stanley, Simpson, Ericka, Lagier-Tourenne, Clotilde, Pulst, Stefan M., Gibson, Summer, Trojanowski, John Q., Elman, Lauren, McCluskey, Leo, Grossman, Murray, Shneider, Neil A., Chung, Wendy K., Ravits, John M., Glass, Jonathan D., Sims, Katherine B., Van Deerlin, Vivianna M., Maniatis, Tom, Hayes, Sebastian D., Ordureau, Alban, Swarup, Sharan, Landers, John, Baas, Frank, Allen, Andrew S., Bedlack, Richard S., Harper, J. Wade, Gitler, Aaron D., Rouleau, Guy A., Brown, Robert, Harms, Matthew B., Cooper, Gregory M., Harris, Tim, Myers, Richard M., Goldstein, David B.

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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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Interventions to improve vitamin D status in at-risk ethnic groups during pregnancy and early childhood: a systematic review von Tanna, Nuttan K, Alexander, Emma C, Lee, Charlotte, Lakhanpaul, Monica, Popat, Rickin M, Almeida-Meza, Pamela, Tuck, Alice, Manikam, Logan, Blair, Mitch

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Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis von Dewan, Ramita, Keagle, Pamela, Bacikova, Dagmar, Soltis, Anthony R., Kost, Jason, Colombrita, Claudia, Lewis, Elizabeth A., Pensato, Viviana, Castellotti, Barbara, McLaughlin, Russell L., Comi, Giacomo P., Ceroni, Mauro, Gagliardi, Stella, van Blitterswijk, Marka, Corrado, Lucia, Sorarù, Gianni, Williams, Kelly L., Morrison, Karen E., Veldink, Jan H., Brown, Robert H., Ambrose, John C., Brittain, H., Elgar, Greg, Halai, Dina, Holman, James E., Jackson, Rob, Leong, Ivonne U.S., Maleady-Crowe, Fiona, Mason, Joanne, Riesgo-Ferreiro, Pablo, Rogers, Tim, Watters, Sarah A., Arepalli, Sampath, Chiò, Adriano, Dunckley, Travis L., Faghri, Faraz, Feldman, Eva, Floeter, Mary Kay, Gerhard, Glenn, Jansson, Lilja, Kirby, Janine, Mora, Gabriele, Nalls, Mike A., Pulst, Stefan M., Ravits, John M., Renton, Alan E., Robberecht, Wim, Robey, Ian, Dols-Icardo, Oriol, Illán-Gala, Ignacio, Lleó, Alberto, Khoshnood, Behzad, Sorbi, Sandro, Pastor, Pau, Bigio, Eileen H., Black, Sandra E., Brunetti, Maura, Canosa, Antonio, Gan-Or, Ziv, Goate, Alison, Hupalo, Daniel, Infante, Jon, Kaufmann, Horacio, Kim, Ronald C., Krüger, Rejko, Logroscino, Giancarlo, Love, Seth, Mao, Qinwen, Masliah, Eliezer, Pletnikova, Olga, Reynolds, Regina H., Scherzer, Clemens R., Serrano, Geidy E., Xiromerisiou, Georgia, Phatnani, Hemali, Kwan, Justin, Broach, James R., Arcila-Londono, Ximena, Malaspina, Andrea, Thompson, Leslie M., Dardiotis, Efthimios, Chandran, Siddharthan, Butovsky, Oleg, Dubnau, Joshua, Harms, Matt, Poss, Mary, Phillips-Cremins, Jennifer, Altschuler, Steven, Hu, Michele T.M., Leigh, P. Nigel, Massey, Luke A., Pavese, Nicola, Vaughan, Jenny, Rowe, James B., Ghidoni, Roberta, Ryten, Mina, Tanaka, Toshiko, Ferrucci, Luigi, Vonsattel, Jean Paul, Landers, John E.

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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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Short-term risk prediction after major lower limb amputation: PERCEIVE study von Gwilym, Brenig L, Pallmann, Philip, Waldron, Cherry-Ann, Thomas-Jones, Emma, Milosevic, Sarah, Brookes-Howell, Lucy, Harris, Debbie, Massey, Ian, Burton, Jo, Stewart, Phillippa, Samuel, Katie, Jones, Sian, Cox, David, Clothier, Annie, Edwards, Adrian, Twine, Christopher P, Bosanquet, David C

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Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth von Loveday, Chey, Tatton-Brown, Katrina, Clarke, Matthew, Westwood, Isaac, Renwick, Anthony, Ramsay, Emma, Nemeth, Andrea, Campbell, Jennifer, Joss, Shelagh, Gardner, McKinlay, Zachariou, Anna, Elliott, Anna, Ruark, Elise, van Montfort, Rob, Rahman, Nazneen

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Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections von Mis, Emily K., Brodsky, Nina N., Ionita, Cristian, Darbinyan, Armine, Drummond-Borg, Margaret, McGee, Elisabeth, Nugent, Kimberly, Ortega, Lucy, Goodkin, Howard P., Sapp, Katie, McKee, Shane, Rea, Gillian, Cooper, Nicola, O’Driscoll, Mary, Scurr, Ingrid, Abbs, Steve, Armstrong, Ruth, Raymond, Lucy, Green, Andrew, Cleary, Elaine, Lampe, Anne, Castle, Bruce, Loughlin, Sam, Izatt, Louise, Roworth, Wendy, Yau, Shu, Jewell, Rosalyn, Sarkar, Ajoy, Canham, Natalie, Burkitt-Wright, Emma, Jones, Elizabeth, Smith, Audrey, Wright, Ronnie, Henderson, Alex, Allen, Zoe, Bernhard, Birgitta, Busby, Louise, Clowes, Virginia, Blair, Edward, Stewart, Alison, Kamath, Arveen, Halai, D., Holman, J.E., Jackson, R., Lopez, F.J., Rogers, T., Savage, K., Sieghart, A., Thomas, E.R.A., Thompson, S.R., Tucci, A., Alejandro, Mercedes E., Amendola, Laura, Andrews, Ashley, Bademci, Guney, Baker, Eva, Baldridge, Dustin, Bamshad, Michael, Bayrak-Toydemir, Pinar, Botto, Lorenzo, Coakley, Terra R., Coggins, Matthew, Cooper, Cynthia M., Cunningham, Michael, Dai, Hongzheng, Duncan, Laura, Fieg, Elizabeth L., Forghani, Irman, Hahn, Sihoun, Hanchard, Neil A., Hayes, Nichole, High, Frances, Hisama, Fuki M., Holm, Ingrid A., Jamal, Fariha, Kennedy, Jennifer, LeBlanc, Kimberly, Macnamara, Ellen F., Maduro, Valerie V., Mak, Bryan, McCauley, Jacob, McGee, Elisabeth, Nickerson, Deborah, Nieves-Rodriguez, Shirley, Novacic, Donna, Pace, Laura, Potocki, Lorraine, Quinlan, Aaron, Raja, Archana N., Robertson, Amy K., Rodan, Lance H., Saporta, Mario, Schaechter, Judy, Signer, Rebecca, Solem, Emily, Solnica-Krezel, Lilianna, Sutton, Shirley, Velinder, Matt, Wheeler, Matthew T., Khokha, Mustafa K.

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Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases von Katz, Olivia L., Wild, K. Taylor, McEldrew, Deborah, Kaur, Maninder, Raible, Sarah, Skraban, Cara M., Zackai, Elaine H., Medne, Livija, Izumi, Kosuke, Fortunato, Sierra, Weatherly, Jamila, Hartman, Tiffiney, Deppen, Paul, Blair, Justin, Devkota, Batsal, Schindler, Emma, Hedrick, Holly L., Peranteau, William, Krantz, Ian D.

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Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height von Tatton-Brown, Katrina, Hanks, Sandra, Ruark, Elise, Zachariou, Anna, Duarte, Silvana Del Vecchio, Ramsay, Emma, Snape, Katie, Murray, Anne, Perdeaux, Elizabeth R, Seal, Sheila, Loveday, Chey, Banka, Siddharth, Clericuzio, Carol, Flinter, Frances, Magee, Alex, McConnell, Vivienne, Patton, Michael, Raith, Wolfgang, Rankin, Julia, Splitt, Miranda, Strenger, Volker, Taylor, Clare, Wheeler, Patricia, Temple, Karen I, Cole, Trevor, Douglas, Jenny, Rahman, Nazneen

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Search for long-lived neutral particles decaying into lepton jets in proton-proton collisions at √s= 8TeV with the ATLAS detector von Aad, Georges, Abbott, Brad, Abdallah, Jalal, Abdel Khalek, Samah, Abdinov, Ovsat Bahram oglu, Aben, Rosemarie, Abi, Babak, Abolins, Maris, AbouZeid, Hass, Abramowicz, Halina, Buanes, Trygve, Dale, Ørjan, Eigen, Gerald, Kastanas, Alex, Liebig, Wolfgang, Lipniacka, Anna, Martin dit Latour, Bertrand, Rosendahl, Peter Lundgaard, Sandaker, Heidi, Sjursen, Therese B, Smestad, Lillian, Stugu, Bjarne, Ugland, Maren, Bugge, Lars, Bugge, Magnar Kopangen, Cameron, David Gordon, Catmore, James Richard, Czyczula, Zofia, Franconi, Laura, Gjelsten, Børge Kile, Gramstad, Eirik, Ould-Saada, Farid, Pajchel, Katarina, Pedersen, Maiken, Read, Alexander Lincoln, Røhne, Ole Myren, Stapnes, Steinar, Strandlie, Are, Abreu, Henso, Abreu, Rômulo F, Adamczyk, Leszek, Adams, David, Adelman, Jareed, Adomeit, Stefanie, Adye, Tim, Agatonovic-Jovin, Tatjana, Aguilar Saavedra, Juan Antonio, Åkerstedt, Henrik, Åkesson, Torsten P.A, Åsman, Barbro, ATLAS, Collaboration

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Clinical testing panels for ALS: global distribution, consistency, and challenges von Dilliott, Allison A., Al Nasser, Ahmad, Elnagheeb, Marwa, Fifita, Jennifer, Henden, Lyndal, Keseler, Ingrid M., Lenz, Steven, Marriott, Heather, Mccann, Emily, Mesaros, Maysen, Opie-Martin, Sarah, Owens, Emma, Palus, Brooke, Ross, Justyne, Wang, Zhanjun, White, Hannah, Al-Chalabi, Ammar, Andersen, Peter M., Benatar, Michael, Blair, Ian, Cooper-Knock, Johnathan, Harrington, Elizabeth A., Heckmann, Jeannine, Landers, John, Moreno, Cristiane, Nel, Melissa, Rampersaud, Evadnie, Roggenbuck, Jennifer, Rouleau, Guy, Traynor, Bryan, Van Blitterswijk, Marka, Van Rheenen, Wouter, Veldink, Jan, Weishaupt, Jochen, Drury, Luke, Harms, Matthew B., Farhan, Sali M. K.

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12/15-Lipoxygenase-Dependent Myeloid Production of Interleukin-12 Is Essential for Resistance to Chronic Toxoplasmosis von Middleton, Melissa K, Zukas, Alicia M, Rubinstein, Tanya, Kinder, Michelle, Wilson, Emma H, Zhu, Peijuan, Blair, Ian A, Hunter, Christopher A, Puré, Ellen

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Phosphorodiamidates as a Promising New Phosphate Prodrug Motif for Antiviral Drug Discovery: Application to Anti-HCV Agents von McGuigan, Christopher, Madela, Karolina, Aljarah, Mohamed, Bourdin, Claire, Arrica, Maria, Barrett, Emma, Jones, Sarah, Kolykhalov, Alexander, Bleiman, Blair, Bryant, K. Dawn, Ganguly, Babita, Gorovits, Elena, Henson, Geoffrey, Hunley, Damound, Hutchins, Jeff, Muhammad, Jerry, Obikhod, Aleksandr, Patti, Joseph, Walters, C. Robin, Wang, Jin, Vernachio, John, Ramamurty, Changalvala V. S, Battina, Srinivas K, Chamberlain, Stanley

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