Progressive Disordered Movements in an Infant Leads to Rare Diagnosis by Pasquale, Sarah, Dam, Aaron, Kelly, Christopher, Schubert, Romaine, Melville, Laura

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12th WINFOCUS world congress on ultrasound in emergency and critical care by Acar, Yahya, Salman, Necati, Cevik, Erdem, Algaba-Montes, Margarita, Patricio-Bordomás, Mayra, Mahmoud, Mustafa Z., Sulieman, Abdelmoneim, Mustafa, Alrayah, Abdelrahman, Ihab, Bahar, Mustafa, Ali, Osama, Lester Kirchner, H., Prosen, Gregor, Anzic, Ajda, Leeson, Paul, Bahreini, Maryam, Hosseinnejad, Houman, Blecher, Gabriel, Meek, Robert, Belina, Stanko, Vančina, Tihomir, Kovačević, Idriz, Rustemović, Nadan, Lee, Jin Hee, Kwak, Young Ho, Kim, Do Kyun, Cheng, Chi-Yung, Pan, Hsiu-Yung, Kung, Chia-Te, Ćurčić, Ela, Pritišanac, Ena, Planinc, Ivo, Medić, Marijana Grgić, Radonić, Radovan, Fasina, Abiola, Fochi, Oliviero, Favarato, Moreno, Bonanomi, Ezio, Ha, Youngrock, Toh, Hongchuen, Harmon, Elizabeth, Chan, Wilma, Baston, Cameron, Morrison, Gail, Shofer, Frances, Hua, Angela, Tsung, James, Gunaydin, Isa, Ay, Mehmet Oguzhan, Kim, Jinjoo, Kim, Jinhyun, Choi, Gyoosung, Shim, Dowon, Lee, Ji-Han, Ambrozic, Jana, Prokselj, Katja, Lucovnik, Miha, Simenc, Gabrijela Brzan, Maleckas, Almantas, Kriščiukaitis, Algimantas, Mačiulis, Vytautas, Macas, Andrius, Mohite, Sharad, Narancsik, Zoltan, Možina, Hugon, Nikolić, Sara, Petrovčič, Rok, Orlob, Simon, Lerchbaumer, Markus, Schönegger, Niklas, Kaufmann, Reinhard, Pan, Chun-I, Pasquale, Sarah, Doniger, Stephanie J., Yellin, Sharon, Chiricolo, Gerardo, Drnovšek, Borut, Leskovar, Boštjan, Robinson, Kristine, Kraft, Clara, Moser, Benjamin, Davis, Stephen, Layman, Shelley, Sayeed, Yusef, Minardi, Joseph, Dzananovic, Amra, Zubovic, Sandra Vegar, Hauptman, Ana Godan, Brajkovic, Ana Vujaklija, Peklic, Marina, Radonic, Vedran, Bielen, Luka, Ming, Peh Wee, Yezid, Nur hafiza, Mohammed, Fatahul Laham, Huda, Zainal Abidin, Ismail, Wan Nasarudin Wan, Isa, W. Yus Haniff W., Fauzi, Hashairi, Mazlan, Mohd Zulfakar

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Progressive Disordered Movements in an Infant Leads to Rare Diagnosis by Pasquale, Sarah, Dam, Aaron, Kelly, Christopher, Schubert, Romaine, Melville, Laura

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Social, economic, and environmental factors influencing the basic reproduction number of COVID-19 across countries by Kong, Jude Dzevela, Tekwa, Edward W, Gignoux-Wolfsohn, Sarah A

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Diagnostic sensitivity and cost per diagnosis of ambulatory cardiac monitoring strategies in unexplained syncope patients by Rogers, John D, Higuera, Lucas, Rosemas, Sarah C, Cheng, Ya-Jian, Ziegler, Paul D

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Single-Cell Genomics Reveals a Novel Cell State During Smooth Muscle Cell Phenotypic Switching and Potential Therapeutic Targets for Atherosclerosis in Mouse and Human by Pan, Huize, Xue, Chenyi, Auerbach, Benjamin J., Fan, Jiaxin, Bashore, Alexander C., Cui, Jian, Yang, Dina Y., Trignano, Sarah B., Liu, Wen, Shi, Jianting, Ihuegbu, Chinyere O., Bush, Erin C., Worley, Jeremy, Vlahos, Lukas, Laise, Pasquale, Solomon, Robert A., Connolly, Edward S., Califano, Andrea, Sims, Peter A., Zhang, Hanrui, Li, Mingyao, Reilly, Muredach P.

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The Use of Antimalarial Drugs against Viral Infection by D'Alessandro, Sarah, Scaccabarozzi, Diletta, Signorini, Lucia, Perego, Federica, Ilboudo, Denise P, Ferrante, Pasquale, Delbue, Serena

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An Artificial Intelligence Approach to Detect Visual Field Progression in Glaucoma Based on Spatial Pattern Analysis by Wang, Mengyu, Shen, Lucy Q, Pasquale, Louis R, Petrakos, Paul, Formica, Sydney, Boland, Michael V, Wellik, Sarah R, De Moraes, Carlos Gustavo, Myers, Jonathan S, Saeedi, Osamah, Wang, Hui, Baniasadi, Neda, Li, Dian, Tichelaar, Jorryt, Bex, Peter J, Elze, Tobias

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A Tripartite Knowledge Translation Program: Innovative Patient-Centered Approach to Clinical Research Participation for Individuals with Multiple Sclerosis by Saini, Aman, Cochran, Colleen, Zucker-Levin, Audrey, Donkers, Sarah J., Kumar, Pawan, Knox, Katherine B., MacPherson, Jessica, Salapa, Hannah, Levin, Michael C.

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Detection of anti-correlation of hot and cold baryons in galaxy clusters by Farahi, Arya, Mulroy, Sarah L., Evrard, August E., Smith, Graham P., Finoguenov, Alexis, Bourdin, Hervé, Carlstrom, John E., Haines, Chris P., Marrone, Daniel P., Martino, Rossella, Mazzotta, Pasquale, O’Donnell, Christine, Okabe, Nobuhiro

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Circulating tumour DNA reflects treatment response and clonal evolution in chronic lymphocytic leukaemia by Yeh, Paul, Hunter, Tane, Sinha, Devbarna, Ftouni, Sarah, Wallach, Elise, Jiang, Damian, Chan, Yih-Chih, Wong, Stephen Q., Silva, Maria Joao, Vedururu, Ravikiran, Doig, Kenneth, Lam, Enid, Arnau, Gisela Mir, Semple, Timothy, Wall, Meaghan, Zivanovic, Andjelija, Agarwal, Rishu, Petrone, Pasquale, Jones, Kate, Westerman, David, Blombery, Piers, Seymour, John F., Papenfuss, Anthony T., Dawson, Mark A., Tam, Constantine S., Dawson, Sarah-Jane

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Determination of the UV Inactivation Constant Under 280 nm UV LED Irradiation for SARS‐CoV‐2 by Biffi, Silvia, Signorini, Lucia, Cattaneo, Luciano, Della Corna, Lorenzo, Guercilena, Andrea, D’Alessandro, Sarah, Ferrante, Pasquale, Delbue, Serena

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LoCuSS: scaling relations between galaxy cluster mass, gas, and stellar content by Mulroy, Sarah L, Farahi, Arya, Evrard, August E, Smith, Graham P, Finoguenov, Alexis, O’Donnell, Christine, Marrone, Daniel P, Abdulla, Zubair, Bourdin, Hervé, Carlstrom, John E, Démoclès, Jessica, Haines, Chris P, Martino, Rossella, Mazzotta, Pasquale, McGee, Sean L, Okabe, Nobuhiro

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Museum anchors and social media: possible nexus and future development by Ruggiero, Pasquale, Lombardi, Rosa, Russo, Sarah

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IRF4 Activity Is Required in Established Plasma Cells to Regulate Gene Transcription and Mitochondrial Homeostasis by Low, Michael Sze Yuan, Brodie, Erica J., Fedele, Pasquale L., Liao, Yang, Grigoriadis, George, Strasser, Andreas, Kallies, Axel, Willis, Simon N., Tellier, Julie, Shi, Wei, Gabriel, Sarah, O’Donnell, Kristy, Pitt, Catherine, Nutt, Stephen L., Tarlinton, David

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Aircraft observations since the 1990s reveal increases of tropospheric ozone at multiple locations across the Northern Hemisphere by Gaudel, Audrey, Cooper, Owen R, Chang, Kai-Lan, Bourgeois, Ilann, Ziemke, Jerry R, Strode, Sarah A, Oman, Luke D, Sellitto, Pasquale, Nédélec, Philippe, Blot, Romain, Thouret, Valérie, Granier, Claire

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The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome by Larsen, Jan, Johannesen, Katrine Marie, Ek, Jakob, Tang, Shan, Marini, Carla, Blichfeldt, Susanne, Kibæk, Maria, Spiczak, Sarah, Weckhuysen, Sarah, Frangu, Mimoza, Neubauer, Bernd Axel, Uldall, Peter, Striano, Pasquale, Zara, Federico, Kleiss, Rebecca, Simpson, Michael, Muhle, Hiltrud, Nikanorova, Marina, Jepsen, Birgit, Tommerup, Niels, Stephani, Ulrich, Guerrini, Renzo, Duno, Morten, Hjalgrim, Helle, Pal, Deb, Helbig, Ingo, Møller, Rikke Steensbjerre, Craiu, DC, Caglayan, HS, Talvik, T, Weber, YG, Barisic, N

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Unveiling the paradox of public administrations' risk and crisis communication during Covid-19 by Russo, Sarah, Ruggiero, Pasquale, Mussari, Riccardo

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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals by Howrigan, Daniel P., Abbott, Liam E., Tashman, Katherine, Singh, Tarjinder, Watts, Nick, Lal, Dennis, Hakonarson, Hakon, Weckhuysen, Sarah, Petrovski, Slavé, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Guerrini, Renzo, Marson, Anthony G., Depondt, Chantal, Striano, Pasquale, Freyer, Catharine, Regan, Brigid M., Leu, Costin, Johns, Esther M.C., Macdonald, Alexandra, Bahlo, Melanie, Todaro, Marian, Stamberger, Hannah, Sadoway, Tara R., Kousiappa, Ioanna, Tanteles, George A., Štěrbová, Katalin, Kunz, Wolfram S., Zsurka, Gábor, Elger, Christian E., Rademacher, Michael, van Baalen, Andreas, von Spiczak, Sarah, Afawi, Zaid, Canavati, Christina, Kluger, Gerhard, Blatt, Ilan, Weber, Yvonne G., Wolking, Stefan, Rau, Sarah, Steinhoff, Bernhard J., Schulze-Bonhage, Andreas, Borggräfe, Ingo, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Chung, Seo-Kyung, Balestrini, Simona, Braatz, Vera, Johnson, Michael R., Auce, Pauls, Sham, Pak C., Lui, Colin H.T., Doherty, Colin P., Shukralla, Arif, El-Naggar, Hany, Vari, Maria Stella, Salpietro, Vincenzo, Tinuper, Paolo, Gagliardi, Monica, Montomoli, Martino, Doccini, Viola, Inoue, Yushi, Yamakawa, Kazuhiro, Tumiene, Birute, Sadleir, Lynette G., Caglayan, S. Hande, Arslan, Mutluay, Yis, Uluc, Topaloglu, Pınar, Baykan, Betül, Salman, Barış, Haryanyan, Garen, Özkara, Çiğdem, Poduri, Annapurna, Shiedley, Beth R., Shain, Catherine, French, Jacqueline A., Kuzniecky, Ruben I., Hegde, Manu, Helbig, Katherine L., Piras, Federica, Reif, Andreas, McQuillin, Andrew, Johnstone, Mandy, Palotie, Aarno, Carvalho, Celia Barreto, Achtyes, Eric D., Azevedo, Maria Helena, Kotov, Roman, Lehrer, Douglas S., Marder, Stephen R., Medeiros, Helena, Morley, Christopher P., Rapaport, Mark H., Knowles, James A., McCarroll, Steven A., Lowenstein, Daniel H., Goldstein, David B.

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Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies by Carvill, Gemma L., Engel, Krysta L., Ramamurthy, Aishwarya, Cochran, J. Nicholas, Roovers, Jolien, Stamberger, Hannah, Lim, Nicholas, Schneider, Amy L., Hollingsworth, Georgie, Holder, Dylan H., Regan, Brigid M., Lawlor, James, Lagae, Lieven, Ceulemans, Berten, Bebin, E. Martina, Nguyen, John, Striano, Pasquale, Zara, Federico, Helbig, Ingo, Møller, Rikke S., von Spiczak, Sarah, Muhle, Hiltrud, Caglayan, Hande, Sterbova, Katalin, Craiu, Dana, Hoffman, Dorota, Lehesjoki, Anna-Elina, Selmer, Kaja, Depienne, Christel, Lemke, Johannes, Marini, Carla, Guerrini, Renzo, Neubauer, Bernd, Talvik, Tiina, Leguern, Eric, de Jonghe, Peter, Weckhuysen, Sarah, Barsh, Gregory S., Weckhuysen, Sarah, Meisler, Miriam, Berkovic, Samuel F., De Jonghe, Peter, Scheffer, Ingrid E., Myers, Richard M., Cooper, Gregory M., Mefford, Heather C.

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