Mutations in the Heme Exporter FLVCR1 Cause Sensory Neurodegeneration with Loss of Pain Perception von Chiabrando, Deborah, Castori, Marco, di Rocco, Maja, Ungelenk, Martin, Gießelmann, Sebastian, Di Capua, Matteo, Madeo, Annalisa, Grammatico, Paola, Bartsch, Sophie, Hübner, Christian A, Altruda, Fiorella, Silengo, Lorenzo, Tolosano, Emanuela, Kurth, Ingo

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National prevalence of larval echinococcosis in sheep in slaughtering plants Ovis aries as an indicator in control programmes in Uruguay von Cabrera, P.A, Irabedra, P, Orlando, D, Rista, L, Harán, G, Viñals, G, Blanco, M.T, Alvarez, M, Elola, S, Morosoli, D, Moraña, A, Bondad, M, Sambrán, Y, Heinzen, T, Chans, L, Piñeyro, L, Pérez, D, Pereyra, I

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De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies von Myers, Candace T., McMahon, Jacinta M., Schneider, Amy L., Petrovski, Slavé, Allen, Andrew S., Carvill, Gemma L., Zemel, Matthew, Saykally, Julia E., LaCroix, Amy J., Heinzen, Erin L., Hollingsworth, Georgina, Nikanorova, Marina, Corbett, Mark, Gecz, Jozef, Coman, David, Freeman, Jeremy, Calvert, Sophie, Gill, Deepak, Carney, Patrick, Lerman-Sagie, Tally, Sampaio, Hugo, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E., Epstein, Michael P., Glauser, Tracy, Johnson, Michael R., Kuzniecky, Ruben, Marson, Anthony G., O’Brien, Terence J., Ottman, Ruth, Petrou, Stephen, Poduri, Annapurna, Pickrell, William O., Chung, Seo-Kyung, Rees, Mark I., Sherr, Elliott, Sadleir, Lynette G., Goldstein, David B., Lowenstein, Daniel H., Møller, Rikke S., Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.

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Distinct neurological disorders with ATP1A3 mutations von Heinzen, Erin L, Dr, Arzimanoglou, Alexis, MD, Brashear, Allison, Prof, Clapcote, Steven J, PhD, Gurrieri, Fiorella, Prof, Goldstein, David B, Prof, Jóhannesson, Sigurður H, Mikati, Mohamad A, Prof, Neville, Brian, Prof, Nicole, Sophie, PhD, Ozelius, Laurie J, PhD, Poulsen, Hanne, PhD, Schyns, Tsveta, PhD, Sweadner, Kathleen J, PhD, van den Maagdenberg, Arn, Prof, Vilsen, Bente, Prof

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Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene von Barba, Carmen, Blumcke, Ingmar, Winawer, Melodie R., Hartlieb, Till, Kang, Hoon-Chul, Grisotto, Laura, Chipaux, Mathilde, Bien, Christian G., Heřmanovská, Barbora, Porter, Brenda E., Lidov, Hart G.W., Cetica, Valentina, Woermann, Friedrich G., Lopez-Rivera, Javier A., Canoll, Peter D., Mader, Irina, D'Incerti, Ludovico, Baldassari, Sara, Yang, Edward, Gaballa, Ahmed, Vogel, Hannes, Straka, Barbora, Macconi, Letizia, Polster, Tilman, Grant, Gerald A., Krsková, Lenka, Shin, Hui Jin, Ko, Ara, Crino, Peter B., Krsek, Pavel, Lee, Jeong Ho, Lal, Dennis, Baulac, Stéphanie, Poduri, Annapurna, Guerrini, Renzo

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Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies von Abou-Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J., Bast, Thomas, Baum, Larry, Becker, Albert J., Becker, Felicitas, Berghuis, Bianca, Berkovic, Samuel F., Boysen, Katja E., Bradfield, Jonathan P., Brody, Lawrence C., Buono, Russell J., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Cavalleri, Gianpiero L., Cherny, Stacey S., Chinthapalli, Krishna, Coffey, Alison J., Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, Craig, John J., de Haan, Gerrit-Jan, De Jonghe, Peter, de Kovel, Carolien G. F., Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Dlugos, Dennis J., Doherty, Colin P., Elger, Christian E., Eriksson, Johan G., Ferraro, Thomas N., Feucht, Martha, Francis, Ben, Franke, Andre, French, Jacqueline A., Freytag, Saskia, Gaus, Verena, Geller, Eric B., Gieger, Christian, Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gui, Hongsheng, Guo, Youling, Haas, Kevin F., Hakonarson, Hakon, Hallmann, Kerstin, Haut, Sheryl, Heinzen, Erin L., Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Ingason, Andrés, Jamnadas-Khoda, Jennifer, Johnson, Michael R., Kälviäinen, Reetta, Kantanen, Anne-Mari, Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Krause, Roland, Krenn, Martin, Kunz, Wolfram S., Kuzniecky, Ruben, Kwan, Patrick, Lal, Dennis, Lau, Yu-Lung, Lehesjoki, Anna-Elina, Lerche, Holger, Leu, Costin, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D., Lopes-Cendes, Iscia, Lowenstein, Daniel H., Malovini, Alberto, Marson, Anthony G., Mayer, Thomas, McCormack, Mark, Mills, James L., Mirza, Nasir, Moerzinger, Martina, Møller, Rikke S., Molloy, Anne M., Muhle, Hiltrud, Newton, Mark, Ng, Ping-Wing, Nöthen, Markus M., Nürnberg, Peter, O’Brien, Terence J., Oliver, Karen L.

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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals von 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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Comparison of woman-specific versus breast-specific data for reporting screening mammography performance von Heinzen, Molly T., Yankaskas, Bonnie C., Kwok, Richard K.

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Polygenic burden in focal and generalized epilepsies von Leu, Costin, Stevelink, Remi, Smith, Alexander W, Goleva, Slavina B, Kanai, Masahiro, Ferguson, Lisa, Campbell, Ciaran, Kamatani, Yoichiro, Okada, Yukinori, Sisodiya, Sanjay M, Cavalleri, Gianpiero L, Koeleman, Bobby P C, Lerche, Holger, Jehi, Lara, Davis, Lea K, Najm, Imad M, Palotie, Aarno, Daly, Mark J, Busch, Robyn M, Lal, Dennis

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Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies von Anon

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Ideology or Experience: A Study of Sexual Harassment von Saperstein, Aron

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Deployment of an Interdisciplinary Predictive Analytics Task Force to Inform Hospital Operational Decision-Making During the COVID-19 Pandemic von Amrami, Kimberly, Domnick, Robert, Heinzen, Ethan, Helfinstine, Karen, Jayakumar, Ajay, Johnson, Patrick, Knepper, Camille, Marcelletti, David, Mickelson, Mindy, Rojas, Ricardo, St. George, Mark, Tande, Aaron, Walvatne, Kelli, Wutthisirisart, Phichet, Pollock, Benjamin D., Carter, Rickey E., Dowdy, Sean C., Dunlay, Shannon M., Habermann, Elizabeth B., Kor, Daryl J., Limper, Andrew H., Liu, Hongfang, Franco, Pablo Moreno, Neville, Matthew R., Noe, Katherine H., Poe, John D., Sampathkumar, Priya, Storlie, Curtis B., Ting, Henry H., Shah, Nilay D.

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Early Clinical Variables Associated With Refractory Convulsive Status Epilepticus in Children von Peariso, Katrina, Arya, Ravindra, Glauser, Tracy, Abend, Nicholas S., Barcia Aguilar, Cristina, Amengual-Gual, Marta, Anderson, Anne, Appavu, Brian L., Brenton, J. Nicholas, Carpenter, Jessica, Chapman, Kevin E., Clark, Justice, Gaillard, William D., Gaínza-Lein, Marina, Goldstein, Joshua, Goodkin, Howard, Grinspan, Zachary, Guerriero, Rejean M., Horn, Paul S., Huh, Linda, Kahoud, Robert, Kelley, Sarah A., Kossoff, Eric H., Kapur, Kush, Lai, Yi-Chen, Marquis, B. Oyinkan, McDonough, Tiffani, Mikati, Mohamad A., Morgan, Lindsey, Novotny, Edward, Ostendorf, Adam P., Payne, Eric T., Piantino, Juan, Riviello, James, Sands, Tristan, Stafstrom, Carl E., Tasker, Robert C., Tchapyjnikov, Dmitry, Vasquez, Alejandra, Wainwright, Mark S., Wilfong, Angus, Williams, Korwyn, Loddenkemper, Tobias

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Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals von Montanucci, Ludovica, Lewis-Smith, David, Collins, Ryan L., Niestroj, Lisa-Marie, Parthasarathy, Shridhar, Xian, Julie, Ganesan, Shiva, Macnee, Marie, Brünger, Tobias, Thomas, Rhys H., Talkowski, Michael, Helbig, Ingo, Leu, Costin, Lal, Dennis

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Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals von Povysil, Gundula, Allen, Andrew S., Howrigan, Daniel P., Tashman, Katherine, Cerrato, Felecia, Cusick, Caroline, Heyne, Henrike, Churchhouse, Claire, Watts, Nick, Lal, Dennis, Gupta, Namrata, Cavalleri, Gianpiero L., Hakonarson, Hakon, Marson, Anthony G., Petrovski, Slavé, Sisodiya, Sanjay M., Depondt, Chantal, Scheffer, Ingrid E., Krause, Roland, Regan, Brigid M., Leu, Costin, Leech, Stephanie L., Todaro, Marian, Stamberger, Hannah, Kousiappa, Ioanna, Tanteles, George A., Christou, Yiolanda, Laššuthová, Petra, Knake, Susanne, Kunz, Wolfram S., Zsurka, Gábor, Surges, Rainer, Rademacher, Annika, von Spiczak, Sarah, Kanaan, Moien, Canavati, Christina, Lemke, Johannes R., Krey, Ilona, Weber, Yvonne G., Wolking, Stefan, Kegele, Josua, Borggräfe, Ingo, Mayer, Thomas, Brockmann, Knut, Madeleyn, Rene, Saarela, Anni, Linnankivi, Tarja, Lehesjoki, Anna-Elina, Derambure, Philippe, Hirsch, Edouard, Chassoux, Francine, Chung, Seo-Kyung, Schneider, Natascha, Balestrini, Simona, Zagaglia, Sara, Johnson, Michael R., Auce, Pauls, Barišić, Nina, Canafoglia, Laura, Franceschetti, Silvana, Castellotti, Barbara, Granata, Tiziana, Ragona, Francesca, Iacomino, Michele, Riva, Antonella, Vari, Maria Stella, Salpietro, Vincenzo, Mancardi, Maria Margherita, Nobili, Lino, Bisulli, Francesca, Pippucci, Tommaso, Licchetta, Laura, Tinuper, Paolo, Gambardella, Antonio, Labate, Angelo, Annesi, Grazia, Manna, Lorella, Parrini, Elena, Bianchini, Claudia, Montomoli, Martino, Hirose, Shinichi, Yamakawa, Kazuhiro, Beydoun, Ahmad, Sadleir, Lynette G., Topaloglu, Pınar, Baykan, Betül, Özkara, YeşÇiğdem, Ho, Chen-Jui, Chou, I-Jun, Shain, Catherine, Goldman, Alicia, Busch, Robyn M., Jehi, Lara, Ferguson, Lisa, Clark, Peggy O., Privitera, Michael, Schachter, Steven, Cosico, Mahgenn, Lowenstein, Daniel H., Goldstein, David B.

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First-line medication dosing in pediatric refractory status epilepticus von Vasquez, Alejandra, Gaínza-Lein, Marina, Abend, Nicholas S., Amengual-Gual, Marta, Anderson, Anne, Arya, Ravindra, Brenton, J. Nicholas, Carpenter, Jessica L., Chapman, Kevin, Clark, Justice, Farias-Moeller, Raquel, Gaillard, William D., Glauser, Tracy, Goldstein, Joshua L., Goodkin, Howard P., Guerriero, Rejean M., Kapur, Kush, Lai, Yi-Chen, McDonough, Tiffani L., Mikati, Mohamad A., Morgan, Lindsey A., Novotny, Edward J., Ostendorf, Adam P., Payne, Eric T., Peariso, Katrina, Piantino, Juan, Riviello, James J., Sannagowdara, Kumar, Tasker, Robert C., Tchapyjnikov, Dmitry, Topjian, Alexis, Wainwright, Mark S., Wilfong, Angus, Williams, Korwyn, Loddenkemper, Tobias, Bansal, Seema, Kelley, Sarah, Stafstrom, Carl, Kossoff, Eric, Habela, Christa, Lewis, Dalila, Stanfield, Tony, Sculier, Claudine, Aguilar, Cristina Barcia, Sansevere, Arnold, Sacco, Melissa, Duncan, Abby, McCoy, Jordan, DaSilva-Chiodo, Kathryn, Faist, Robert, Santel, Daniel, LaFay, Victor, Clark, Peggy, Borror, Sarah, Debs, Andrea, Clohessy, Caitlin, Weber, Amanda, Yuliati, Asri, Luat, Aimee, Singh, Azara, Helseth, Ashley, Turner, David, Fernandes, Cecilia, Tran, Linh, McLean, Melissa, Nayak, Anuranjita, Riviello, James J, Hecox, Kurt, Nallamothu, Rupa, Rehborg, Rebecca, Goldstein, David, Heinzen Cox, Erin, Malone, Colin, Thornburg, Olivia, Grinspan, Zachary, Basma, Natasha, Appavu, Brian, Burrows, Brian, Dyar, Beata, Mishler, Laura, Lee-Eng, Jacqueline, Streb, Madison, Hahn, Cecil, Lalgudi Ganesan, Saptharishi (Rishi), Huh, Linda, Martic, Nela

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The Epilepsy Genetics Initiative: Systematic reanalysis of diagnostic exomes increases yield von Berkovic, Samuel F., Goldstein, David B., Heinzen, Erin L., Laughlin, Brandon L., Lowenstein, Daniel H., Lubbers, Laura, Stewart, Randall, Whittemore, Vicky, Angione, Kaitlin, Bazil, Carl W., Bier, Louise, Bluvstein, Judith, Brimble, Elise, Campbell, Colleen, Cavalleri, Gianpiero, Chambers, Chelsea, Choi, Hyunmi, Cilio, Maria Roberta, Ciliberto, Michael, Cornes, Susannah, Delanty, Norman, Demarest, Scott, Devinsky, Orrin, Dlugos, Dennis, Dubbs, Holly, Dugan, Patricia, Ernst, Michelle E., Gibbons, Melissa, Goodkin, Howard P., Helbig, Ingo, Jansen, Laura, Johnson, Kaleas, Joshi, Charuta, Lippa, Natalie C., Marsh, Eric, Martinez, Alejandro, Millichap, John, Mulhern, Maureen S., Numis, Adam, Park, Kristen, Pippucci, Tommaso, Poduri, Annapurna, Porter, Brenda, Regan, Brigid, Sands, Tristan T., Scheffer, Ingrid E., Schreiber, John M., Sheidley, Beth, Singhal, Nilika, Smith, Lacey, Sullivan, Joseph, Taylor, Alan, Tolete, Patricia, Afgani, Tahseen M., Aggarwal, Vimla, Burgess, Rosemary, Dixon‐Salazar, Tracy, Hemati, Parisa, Milder, Julie, Petrovski, Slavé, Revah‐Politi, Anya, Stong, Nicholas

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Epi4K: Gene discovery in 4,000 genomes

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Development and validation of a simple web‐based tool for early prediction of COVID‐19‐associated death in kidney transplant recipients von Modelli de Andrade, Luis Gustavo, Sandes‐Freitas, Tainá Veras, Requião‐Moura, Lúcio R., Viana, Laila Almeida, Cristelli, Marina Pontello, Garcia, Valter Duro, Alcântara, Aline Lima Cunha, Esmeraldo, Ronaldo de Matos, Abbud Filho, Mario, Pacheco‐Silva, Alvaro, Lima Carneiro, Erika Cristina Ribeiro, Manfro, Roberto Ceratti, Costa, Kellen Micheline Alves Henrique, Simão, Denise Rodrigues, Sousa, Marcos Vinicius, Santana, Viviane Brandão Bandeira de Mello, Noronha, Irene L., Romão, Elen Almeida, Zanocco, Juliana Aparecida, Arimatea, Gustavo Guilherme Queiroz, De Boni Monteiro de Carvalho, Deise, Tedesco‐Silva, Helio, Medina‐Pestana, José, Keitel, Elizete, Costa de Oliveira, Claudia Maria, Neri, Beatriz de Oliveira, Fernandes Charpiot, Ida Maria Maximina, Ferreira, Teresa Cristina Alves, Vicari, Alessandra Rosa, Pereira, Tomás, Coelho, Maria Eduarda Heinzen de Almeida, Mazzali, Marilda, Ferreira, Gustavo Fernandes, Campos, Juliana Bastos, Rocha, Nicole Gomes Campos, Saldanha, Anita Leme da Rocha, Martinez, Tania Leme da Rocha, Romão, João Egídio, Teixeira Araújo, Maria Regina, Braga, Sibele Lessa, Deboni, Luciane Mônica, Krüger, Franco Silveira da Mota, Neto, Miguel Moysés, Claudino, Auro Buffani, Cláudio de Oliveira, Lívia, Matuck, Tereza Azevedo, Bignelli, Alexandre Tortoza, Hokazono, Silvia Regina, Suassuna, José Hermógenes Rocco, Rioja, Suzimar da Silveira, Madeira, Rafael Lage, Vilaça, Sandra Simone, Calazans, Carlos Alberto Chalabi, Calazans, Daniel Costa Chalabi, Malafronte, Patrícia, Miorin, Antonio, Aguiar, Filipe Carrilho, Andrade, Larissa Guedes da Fonte, Carvalho, Fabiana Loss, Martins, Karoline Sesiuk, Pinheiro, Hélady Sanders, Sertório, Emiliana Spadarotto, Pereira, André Barreto, Machado, David José Barros, Pozzi, Carolina Maria, Kroth, Leonardo Viliano, Filho, Lauro Monteiro Vasconcellos, Maciel, Rafael Fabio, Silva, Amanda Maíra Damasceno, Baptista, Ana Paula Maia, de Souza, Pedro Augusto Macedo, Lasmar, Marcus Faria, Saber, Luciana Tanajura Santamaria, Palma, Lilian Monteiro Pereira, de Barros Almeida, Ricardo Augusto Monteiro

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Diverse genetic causes of polymicrogyria with epilepsy von Allen, Andrew S, Aggarwal, Vimla, Berkovic, Samuel F, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Guerrini, Renzo, Glauser, Tracy, Heinzen, Erin L, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Poduri, Annapurna, Petrou, Stephen, Petrovski, Slavé, Ruzzo, Elizabeth K, Scheffer, Ingrid E, Sherr, Elliott H, Abou‐Khalil, Bassel, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Berkovic, Samuel F., Bluvstein, Judith, Boro, Alexis, Cascino, Greg, Consalvo, Damian, Crumrine, Pat, Devinsky, Orrin, Dlugos, Dennis, Fountain, Nathan, Freyer, Catharine, Friedman, Dan, Geller, Eric, Glynn, Simon, Haas, Kevin, Haut, Sheryl, Joshi, Sucheta, Kirsch, Heidi, Knowlton, Robert, Kossoff, Eric, Kuzniecky, Ruben, Lowenstein, Daniel H., Motika, Paul V., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack M., Poduri, Annapurna, Scheffer, Ingrid, Shellhaas, Renée A., Sherr, Elliott H., Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K., Sperling, Michael, Smith, Michael C., Sullivan, Joseph, Vining, Eileen P. G., Von Allmen, Gretchen K., Widdess‐Walsh, Peter, Winawer, Melodie R., Bautista, Jocelyn, Fiol, Miguel, Glauser, Tracy, Hayward, Jean, Helmers, Sandra, Park, Kristen, Sirven, Joseph, Lin Thio, Liu, Venkat, Anu, Weisenberg, Judith, Kuperman, Rachel, McGuire, Shannon, Novotny, Edward, Sadleir, Lynette

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