Initial Integrated Strategic Sustainability Plan for Fort Leonard Wood von Palmer, Kevin J, Nemeth, Sarah B, Stumpf, Annette L, Bevelheimer, Susan J

Volltext bestellen

Army Overseas Water Sustainability Study von Jenicek, Elisabeth M, Myers, Natalie R, Curvey, Laura, Nemeth, Sarah B

Volltext bestellen

Predicting Future Training Opportunities Using the Land-Use Evolution and Impact Assessment Model von Westervelt, James D, Nemeth, Sarah B, White, Michael J, Kemme, Michael R, Morrison, Dawn A, Eastgate, Christa, Ginsberg, Mark

Volltext bestellen

Physiological Changes in Extracellular Calcium Concentration Directly Control Osteoblast Function in the Absence of Calciotropic Hormones von Dvorak, Melita M., Siddiqua, Ashia, Ward, Donald T., Carter, D. Howard, Dallas, Sarah L., Nemeth, Edward F., Riccardi, Daniela, Burg, Maurice B.

Volltext

IL-6 mediates hypoferremia of inflammation by inducing the synthesis of the iron regulatory hormone hepcidin von Nemeth, Elizabeta, Rivera, Seth, Gabayan, Victoria, Keller, Charlotte, Taudorf, Sarah, Pedersen, Bente K, Ganz, Tomas

Volltext

Physical Activity Assessment and Counseling in Pediatric Clinical Settings von Lobelo, Felipe, Muth, Natalie D, Hanson, Sara, Nemeth, Blaise A

Volltext

Organized Sports for Children, Preadolescents, and Adolescents von Logan, Kelsey, Cuff, Steven

Volltext

Altered juvenile fish communities associated with invasive Halophila stipulacea seagrass habitats in the U.S. Virgin Islands von Olinger, Lauren K, Heidmann, Sarah L, Durdall, Allie N, Howe, Colin, Ramseyer, Tanya, Thomas, Sara G, Lasseigne, Danielle N, Brown, Elizabeth J, Cassell, John S, Donihe, Michele M, Duffing Romero, Mareike D, Duke, Mara A, Green, Damon, Hillbrand, Paul, Wilson Grimes, Kristin R, Nemeth, Richard S, Smith, Tyler B, Brandt, Marilyn

Volltext

An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy von Pagnamenta, Alistair T, Kaiyrzhanov, Rauan, Zou, Yaqun, Da'as, Sahar I, Maroofian, Reza, Donkervoort, Sandra, Dominik, Natalia, Lauffer, Marlen, Ferla, Matteo P, Orioli, Andrea, Giess, Adam, Tucci, Arianna, Beetz, Christian, Sedghi, Maryam, Ansari, Behnaz, Barresi, Rita, Basiri, Keivan, Cortese, Andrea, Elgar, Greg, Fernandez-Garcia, Miguel A, Yip, Janice, Foley, A Reghan, Gutowski, Nicholas, Jungbluth, Heinz, Lassche, Saskia, Lavin, Tim, Marcelis, Carlo, Marks, Peter, Marini-Bettolo, Chiara, Medne, Livija, Moslemi, Ali-Reza, Sarkozy, Anna, Reilly, Mary M, Muntoni, Francesco, Millan, Francisca, Muraresku, Colleen C, Need, Anna C, Nemeth, Andrea H, Neuhaus, Sarah B, Norwood, Fiona, O'Donnell, Marie, O'Driscoll, Mary, Rankin, Julia, Yum, Sabrina W, Zolkipli-Cunningham, Zarazuela, Brusius, Isabell, Wunderlich, Gilbert, Karakaya, Mert, Wirth, Brunhilde, Fakhro, Khalid A, Tajsharghi, Homa, Bönnemann, Carsten G, Taylor, Jenny C, Houlden, Henry

Volltext

Safety and efficacy of eculizumab in anti-acetylcholine receptor antibody-positive refractory generalised myasthenia gravis (REGAIN): a phase 3, randomised, double-blind, placebo-c... von Utsugisawa, Kimiaki, Kissel, John T, O'Brien, Fanny, Lamont, Phillipa, Roberts, Leslie, De Mey, Katrien, Tilkin, Petra, Alves de Siqueira Carvalho, Alzira, Paiva, Gabriel, Prando, Natalia, Souza, Iandra, Campbell, Natasha, Blackmore, Derrick, Autzen, Anne Mette, Harrison, Tuula, Moutarde, Julie, Le Masson, Gwendal, Wilson, Amy, Fricke, Karin, Horvath, Melinda, Matolcsi, Judit, Szabadosne, Brigitta, Vecsei, Laszlo, Konyane, Monika, Troili, Fernanda, Di Pasquale, Antonella, Filla, Alessandro, Campanella, Angela, Inghilleri, Maurizio, Fionda, Laura, Gabriele, Maria, Salvatore Caramma, Andrea, Kanzaki, Akiko, Jingu, Maki, Yoshimura, Shunsuke, Kobashikawa, Tomomi, Yamashita, Yumi, Kawamura, Tomohiro, Higuchi, Eriko, Osakada, Kaori, Hisahara, Shin, Suzuki, Shuichiro, Ogasawara, Junichi, Shinozaki, Hirokazu, Gibson, Tamar, Keijzers, Maria Johanna, Kim, Byung-Jo, Ra, HyeJin, Kim, Byoung Joon, Lee, JiEun, Kim, Seung Min, Kim, Yool-hee, Lee, Hyung Seok, Yarmoschuk, Asya, Nesterova, Yulia, Fernandez-Fournier, Mireya, Hietala, Albert, Andersson, Blanka, Boz, Cavit, Erdem-Ozdamar, Sevim, Terzi, Murat, Gollogly, Jakit, Smalley, Nicole, Silvestri, Nicholas, Loor, John, Pascuzzi, Robert, Snook, Riley, Carter, Cynthia, Levine-Weinberg, Mark, Simpson, Ericka, Kaur, Harpreet, Crabtree, Brigid, Taber, Sandra, Gilchrist, James, Darnell, Taylor, Goyal, Neelam, Sakamuri, Sarada, Jones, Floyd, Alsharabati, Mohammad, Butters, Janelle, Goyal, Namita, Garcia, Sonia, Echevarria, Laura, Pulley, Michael, Shabbir, Yasmeen, Gutmann, Laurie, Gutmann, Ludwig, Hafer-Macko, Charlene, Chopra, Manisha, Kaufman, Jacob, McClain, Terry, Harvey, Brittany, Huynh, Kristin, Droker, Brian, Weiss, Michael, Downing, Sharon, Bernitsas, Evanthia, Kumar Sriwastava, Shitiz, Jia, Kelly, Patwa, Huned

Volltext

Germline selection shapes human mitochondrial DNA diversity von Wei, Wei, Tuna, Salih, Keogh, Michael J, Smith, Katherine R, Aitman, Timothy J, Beales, Phil L, Bennett, David L, Gale, Daniel P, Bitner-Glindzicz, Maria A K, Black, Graeme C, Brennan, Paul, Elliott, Perry, Flinter, Frances A, Floto, R Andres, Houlden, Henry, Irving, Melita, Koziell, Ania, Maher, Eamonn R, Markus, Hugh S, Morrell, Nicholas W, Newman, William G, Roberts, Irene, Sayer, John A, Smith, Kenneth G C, Taylor, Jenny C, Watkins, Hugh, Webster, Andrew R, Wilkie, Andrew O M, Williamson, Catherine, Ashford, Sofie, Penkett, Christopher J, Stirrups, Kathleen E, Rendon, Augusto, Ouwehand, Willem H, Bradley, John R, Raymond, F Lucy, Caulfield, Mark, Turro, Ernest, Chinnery, Patrick F

Volltext

Quantitative Oculomotor Assessment in Hereditary Ataxia: Discriminatory Power, Correlation with Severity Measures, and Recommended Parameters for Specific Genotypes von Garces, Pilar, Antoniades, Chrystalina A., Sobanska, Anna, Kovacs, Norbert, Ying, Sarah H., Gupta, Anoopum S., Perlman, Susan, Szmulewicz, David J., Pane, Chiara, Németh, Andrea H., Jardim, Laura B., Coarelli, Giulia, Dankova, Michaela, Traschütz, Andreas, Tarnutzer, Alexander A.

Volltext

Quantitative Oculomotor Assessment in Hereditary Ataxia: Systematic Review and Consensus by the Ataxia Global Initiative Working Group on Digital-motor Biomarkers von Garces, Pilar, Antoniades, Chrystalina A., Sobanska, Anna, Kovacs, Norbert, Ying, Sarah H., Gupta, Anoopum S., Perlman, Susan, Szmulewicz, David J., Pane, Chiara, Németh, Andrea H., Jardim, Laura B., Coarelli, Giulia, Dankova, Michaela, Traschütz, Andreas, Tarnutzer, Alexander A.

Volltext

Quantitative Gait and Balance Outcomes for Ataxia Trials: Consensus Recommendations by the Ataxia Global Initiative Working Group on Digital-Motor Biomarkers von Ilg, Winfried, Milne, Sarah, Schmitz-Hübsch, Tanja, Alcock, Lisa, Beichert, Lukas, Bertini, Enrico, Mohamed Ibrahim, Norlinah, Dawes, Helen, Gomez, Christopher M., Hanagasi, Hasmet, Kinnunen, Kirsi M., Minnerop, Martina, Németh, Andrea H., Newman, Jane, Ng, Yi Shiau, Rentz, Clara, Samanci, Bedia, Shah, Vrutangkumar V., Summa, Susanna, Vasco, Gessica, McNames, James, Horak, Fay B.

Volltext

Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder von Kour, Sukhleen, Rajan, Deepa S., Fortuna, Tyler R., Anderson, Eric N., Ward, Caroline, Lee, Youngha, Lee, Sangmoon, Shin, Yong Beom, Chae, Jong-Hee, Choi, Murim, Siquier, Karine, Cantagrel, Vincent, Amiel, Jeanne, Stolerman, Elliot S., Barnett, Sarah S., Cousin, Margot A., Castro, Diana, McDonald, Kimberly, Kirmse, Brian, Nemeth, Andrea H., Rajasundaram, Dhivyaa, Innes, A. Micheil, Lynch, Danielle, Frosk, Patrick, Collins, Abigail, Gibbons, Melissa, Yang, Michele, Desguerre, Isabelle, Boddaert, Nathalie, Gitiaux, Cyril, Rydning, Siri Lynne, Selmer, Kaja K., Urreizti, Roser, Garcia-Oguiza, Alberto, Osorio, Andrés Nascimento, Verdura, Edgard, Pujol, Aurora, McCurry, Hannah R., Landers, John E., Agnihotri, Sameer, Andriescu, E. Corina, Moody, Shade B., Phornphutkul, Chanika, Sacoto, Maria J. Guillen, Begtrup, Amber, Houlden, Henry, Kirschner, Janbernd, Schorling, David, Rudnik-Schöneborn, Sabine, Strom, Tim M., Leiz, Steffen, Juliette, Kali, Richardson, Randal, Yang, Ying, Zhang, Yuehua, Wang, Minghui, Wang, Jia, Wang, Xiaodong, Platzer, Konrad, Donkervoort, Sandra, Bönnemann, Carsten G., Wagner, Matias, Issa, Mahmoud Y., Elbendary, Hasnaa M., Stanley, Valentina, Maroofian, Reza, Gleeson, Joseph G., Zaki, Maha S., Senderek, Jan, Pandey, Udai Bhan

Volltext

Prevalence, distribution, and diversity of cryptic piroplasm infections in raccoons from selected areas of the United States and Canada von Garrett, Kayla B., Hernandez, Sonia M., Balsamo, Gary, Barron, Heather, Beasley, James C., Brown, Justin D., Cloherty, Erin, Farid, Hossain, Gabriel, Mourad, Groves, Bethany, Hamer, Sarah, Hill, Julia, Lewis, Meghan, McManners, Katie, Nemeth, Nicole, Oesterle, Paul, Ortiz, Sebastian, Peshock, Lea, Schnellbacher, Rodney, Schott, Renee, Straif-Bourgeois, Susanne, Yabsley, Michael J.

Volltext

Neuropathy target esterase activity defines phenotypes among PNPLA6 disorders von Liu, James, He, Yi, Lwin, Cara, Han, Marina, Guan, Bin, Naik, Amelia, Bender, Chelsea, Moore, Nia, Huryn, Laryssa A, Sergeev, Yuri V, Qian, Haohua, Zeng, Yong, Dong, Lijin, Liu, Pinghu, Lei, Jingqi, Haugen, Carl J, Prasov, Lev, Shi, Ruifang, Dollfus, Hélène, Aristodemou, Petros, Laich, Yannik, Németh, Andrea H, Taylor, John, Downes, Susan, Krawczynski, Maciej R, Meunier, Isabelle, Strassberg, Melissa, Tenney, Jessica, Gao, Josephine, Shear, Matthew A, Moore, Anthony T, Duncan, Jacque L, Menendez, Beatriz, Hull, Sarah, Vincent, Andrea L, Siskind, Carly E, Traboulsi, Elias I, Blackstone, Craig, Sisk, Robert A, Miraldi Utz, Virginia, Webster, Andrew R, Michaelides, Michel, Arno, Gavin, Synofzik, Matthis, Hufnagel, Robert B

Volltext

A Phylogeny-aware GWAS Framework to Correct for Heritable Pathogen Effects on Infectious Disease Traits von Nadeau, Sarah, Thorball, Christian W, Kouyos, Roger, Günthard, Huldrych F, Böni, Jürg, Yerly, Sabine, Perreau, Matthieu, Klimkait, Thomas, Rauch, Andri, Hirsch, Hans H, Cavassini, Matthias, Vernazza, Pietro, Bernasconi, Enos, Fellay, Jacques, Mitov, Venelin, Stadler, Tanja

Volltext

Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy von Bott, Laura C, Forouhan, Mitra, Lieto, Maria, Sala, Ambre J, Ellerington, Ruth, Johnson, Janel O, Speciale, Alfina A, Criscuolo, Chiara, Filla, Alessandro, Chitayat, David, Alkhunaizi, Ebba, Shannon, Patrick, Nemeth, Andrea H, Angelucci, Francesco, Lim, Wooi Fang, Striano, Pasquale, Zara, Federico, Helbig, Ingo, Muona, Mikko, Courage, Carolina, Lehesjoki, Anna-Elina, Berkovic, Samuel F, Fischbeck, Kenneth H, Brancati, Francesco, Morimoto, Richard I, Wood, Matthew J A, Rinaldi, Carlo

Volltext

A randomized, double-blind, placebo-controlled study of latrepirdine in patients with mild to moderate Huntington disease von Kieburtz, K, Noonberg, S, Seitz, W, Walker, F, De Souza, J, Di Pietro, A, Ferland, G, Chouinard, S, Nemeth, AH, Merritt, C, St Marie, P, Berila, RA, Kubu, C, Segro, V, Wyne, S, Parida, D, Nowak, M, Dziadkiewicz, A, Suter, G, Tan, J, Seeberger, L, Champion, J, Wojcieszek, J, Squitieri, F, Nichols, P, Hoglund, AV, Kieni, J, Wojcik, M, Megens, J, Jenkins, M, Rosas, D, Schindler, C, McNees, AA, Say, M, Panegyres, P, Lewis, N, Jukich, S, Faull, C, Nielsen, TR, Nielsen, JE, Kostyk, S, Agrawal, P, Lear, J, Steiner, T, Stamm, C, Uhl, I, O'Donovan, K, Nevitt, L, Kipps, C, Hayward, E, Mannaa, B, Cormio, C, Di Maio, L, Russo, CV, Sacca, F, Salvatore, E, Wolz, M, Wolz, A, Spruth, E, Gelderblom, H, Priller, J, Sass, C, Probst, D, Leavitt, BR, Coleman, A, Baynes, K, Haske-Palomino, M, Goldstein, J, Peavy, G, Rodriguez, R, Suelter, M, Smith, MM, Dubinsky, H, Craufurd, D, Quesada, M, Rodriguez-Spengler, K, Hoelzner, EM, Colcher, A, Maccarone, H, Siderowf, A, Lucarelli, N, Ivanco, L, Hickey, C, Trautmann, S, Eschenbach, C, Samii, A, Zielonka, D, Marcinkowski, JT, Sempolowicz, J, Witkowski, G, Antczak, J, Richter, P, Jachinska, K, Deppen, P, Wharton, K, Mahant, N, Loy, C, Fisher, D, White, K, Fischer, W

Volltext