COMPUTER-IMPLEMENTED, AUTOMATED MEDIA PLANNING METHOD AND SYSTEM von CURMI NANCY E, PARVAR ALIREZA JAHAN, O'LOUGHLIN ERIN E, WESTFALL EMILY A, STRNAD KAREN, WORONA STEVE, KULA KAREN F, SHERR DANIEL D, DONOHUE DEBRA L, MULVEY THERESE, CLARK LUCY MILLER, STEWART MARY RAINER, KAUL CHRIS

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COMPUTER-IMPLEMENTED, AUTOMATED MEDIA PLANNING METHOD AND SYSTEM von CURMI NANCY E, PARVAR ALIREZA JAHAN, O'LOUGHLIN ERIN E, WESTFALL EMILY A, STRNAD KAREN, WORONA STEVE, KULA KAREN F, SHERR DANIEL D, DONOHUE DEBRA L, MULVEY THERESE, CLARK LUCY MILLER, STEWART MARY RAINER, KAUL CHRIS

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COMPUTER-IMPLEMENTED, AUTOMATED MEDIA PLANNING METHOD AND SYSTEM von CURMI NANCY E, PARVAR ALIREZA JAHAN, O'LOUGHLIN ERIN E, WESTFALL EMILY A, STRNAD KAREN, WORONA STEVE, KULA KAREN F, SHERR DANIEL D, DONOHUE DEBRA L, MULVEY THERESE, CLARK LUCY MILLER, STEWART MARY RAINER, KAUL CHRIS

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COMPUTER-IMPLEMENTED, AUTOMATED MEDIA PLANNING METHOD AND SYSTEM von CURMI, NANCY E, CLARK, LUCY MILLER, KAUL, CHRIS, SHERR, DANIEL D, WESTFALL, EMILY A, MULVEY, THERESE, KULA, KAREN F, PARVAR, ALIREZA JAHAN, DONOHUE, DEBRA L, WORONA, STEVE, STRNAD, KAREN, STEWART, MARY RAINER, O'LOUGHLIN, ERIN E

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COMPUTER-IMPLEMENTED, AUTOMATED MEDIA PLANNING METHOD AND SYSTEM von CURMI, NANCY E, CLARK, LUCY MILLER, KAUL, CHRIS, SHERR, DANIEL D, WESTFALL, EMILY A, MULVEY, THERESE, KULA, KAREN F, PARVAR, ALIREZA JAHAN, DONOHUE, DEBRA L, WORONA, STEVE, STRNAD, KAREN, STEWART, MARY RAINER, O'LOUGHLIN, ERIN E

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COMPUTER-IMPLEMENTED, AUTOMATED MEDIA PLANNING METHOD AND SYSTEM von CURMI, NANCY E, CLARK, LUCY MILLER, KAUL, CHRIS, SHERR, DANIEL D, WESTFALL, EMILY A, MULVEY, THERESE, KULA, KAREN F, PARVAR, ALIREZA JAHAN, DONOHUE, DEBRA L, WORONA, STEVE, STRNAD, KAREN, STEWART, MARY RAINER, O'LOUGHLIN, ERIN E

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Ultra-rare genetic variation in common epilepsies: a case-control sequencing study von Allen, Andrew S, Bellows, Susannah T, Berkovic, Samuel F, Bridgers, Joshua, Burgess, Rosemary, Cavalleri, Gianpiero, Chung, Seo-Kyung, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Heinzen, Erin L, Hildebrand, Michael S, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mayeux, Richard, Mebane, Caroline, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Petrou, Steven, Petrovski, Slavgé, Pickrell, William O, Poduri, Annapurna, Radtke, Rodney A, Rees, Mark I, Regan, Brigid M, Ren, Zhong, Scheffer, Ingrid E, Sills, Graeme J, Thomas, Rhys H, Wang, Quanli, Abou-Khalil, Bassel, Alldredge, Brian K, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Bautista, Jocelyn F., Bluvstein, Judith, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Geller, Eric B, Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R, Hayward, Jean, Helmers, Sandra L, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Sadleir, Lynette G, Shellhaas, Renée A., Sherr, Elliott H, Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Thio, Liu Lin, Venkat, Anu, Vining, Eileen P.G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

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De novo mutations in epileptic encephalopathies von Allen, Andrew S, Berkovic, Samuel F, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E, Epstein, Michael P, Glauser, Tracy, Goldstein, David B, Han, Yujun, Heinzen, Erin L, Hitomi, Yuki, Howell, Katherine B, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Lu, Yi-Fan, Madou, Maura R Z, Marson, Anthony G, Mefford, Heather C, Esmaeeli Nieh, Sahar, O'Brien, Terence J, Ottman, Ruth, Petrovski, Slavé, Poduri, Annapurna, Ruzzo, Elizabeth K, Scheffer, Ingrid E, Sherr, Elliott H, Yuskaitis, Christopher J, Abou-Khalil, Bassel, Alldredge, Brian K, Bautista, Jocelyn F, Boro, Alex, Cascino, Gregory D, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Fiol, Miguel, Fountain, Nathan B, French, Jacqueline, Friedman, Daniel, Geller, Eric B, Glynn, Simon, Haut, Sheryl R, Hayward, Jean, Helmers, Sandra L, Joshi, Sucheta, Kanner, Andres, Kirsch, Heidi E, Knowlton, Robert C, Kossoff, Eric H, Kuperman, Rachel, McGuire, Shannon M, Motika, Paul V, Novotny, Edward J, Paolicchi, Juliann M, Parent, Jack M, Park, Kristen, Shellhaas, Renée A, Shih, Jerry J, Singh, Rani, Sirven, Joseph, Smith, Michael C, Sullivan, Joseph, Lin Thio, Liu, Venkat, Anu, Vining, Eileen P G, Von Allmen, Gretchen K, Weisenberg, Judith L, Widdess-Walsh, Peter, Winawer, Melodie R

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Consensus Recommendations for the Use of Automated Insulin Delivery Technologies in Clinical Practice von Phillip, Moshe, Nimri, Revital, Bergenstal, Richard M, Barnard-Kelly, Katharine, Danne, Thomas, Hovorka, Roman, Kovatchev, Boris P, Messer, Laurel H, Parkin, Christopher G, Ambler-Osborn, Louise, Amiel, Stephanie A, Bally, Lia, Beck, Roy W, Biester, Sarah, Biester, Torben, Blanchette, Julia E, Bosi, Emanuele, Boughton, Charlotte K, Breton, Marc D, Brown, Sue A, Buckingham, Bruce A, Cai, Albert, Carlson, Anders L, Castle, Jessica R, Choudhary, Pratik, Close, Kelly L, Cobelli, Claudio, Criego, Amy B, Davis, Elizabeth, de Beaufort, Carine, de Bock, Martin I, DeSalvo, Daniel J, DeVries, J Hans, Dovc, Klemen, Doyle, Francis J, Ekhlaspour, Laya, Shvalb, Naama Fisch, Forlenza, Gregory P, Gallen, Geraldine, Garg, Satish K, Gershenoff, Dana C, Gonder-Frederick, Linda A, Haidar, Ahmad, Hartnell, Sara, Heinemann, Lutz, Heller, Simon, Hirsch, Irl B, Hood, Korey K, Isaacs, Diana, Klonoff, David C, Kordonouri, Olga, Kowalski, Aaron, Laffel, Lori, Lawton, Julia, Lal, Rayhan A, Leelarathna, Lalantha, Maahs, David M, Murphy, Helen R, Nørgaard, Kirsten, O’Neal, David, Oser, Sean, Oser, Tamara, Renard, Eric, Riddell, Michael C, Rodbard, David, Russell, Steven J, Schatz, Desmond A, Shah, Viral N, Sherr, Jennifer L, Simonson, Gregg D, Wadwa, R Paul, Ward, Candice, Weinzimer, Stuart A, Wilmot, Emma G, Battelino, Tadej

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Oceanic Protists von SHERR, BARRY F., SHERR, EVELYN B., CARON, DAVID A., VAULOT, DANIEL, WORDEN, ALEXANDRA Z.

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De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects von Accogli, Andrea, Calabretta, Sara, St-Onge, Judith, Boudrahem-Addour, Nassima, Dionne-Laporte, Alexandre, Joset, Pascal, Azzarello-Burri, Silvia, Rauch, Anita, Krier, Joel, Fieg, Elizabeth, Pallais, Juan C, McConkie-Rosell, Allyn, McDonald, Marie, Freedman, Sharon F, Rivière, Jean-Baptiste, Lafond-Lapalme, Joël, Simpson, Brittany N, Hopkin, Robert J, Trimouille, Aurélien, Van-Gils, Julien, Begtrup, Amber, McWalter, Kirsty, Delphine, Heron, Keren, Boris, Genevieve, David, Argilli, Emanuela, Sherr, Elliott H, Severino, Mariasavina, Rouleau, Guy A, Yam, Patricia T, Charron, Frédéric, Srour, Myriam

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Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis von Qian, Xuyu, DeGennaro, Ellen M, Talukdar, Maya, Akula, Shyam K, Lai, Abbe, Shao, Diane D, Gonzalez, Dilenny, Marciano, Jack H, Smith, Richard S, Hylton, Norma K, Yang, Edward, Bazan, J Fernando, Barrett, Lee, Yeh, Rebecca C, Hill, R Sean, Beck, Samantha G, Otani, Aoi, Angad, Jolly, Mitani, Tadahiro, Posey, Jennifer E, Pehlivan, Davut, Calame, Daniel, Aydin, Hatip, Yesilbas, Osman, Parks, Kendall C, Argilli, Emanuela, England, Eleina, Im, Kiho, Taranath, Ajay, Scott, Hamish S, Barnett, Christopher P, Arts, Peer, Sherr, Elliott H, Lupski, James R, Walsh, Christopher A

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The role of copy number variants in the genetic architecture of common familial epilepsies von Almanza Fuerte, Edith P., Nguyen, John, Mehaffey, Michelle, Sulovari, Arvis, Wang, Tianyun, Galey, Miranda, Miller, Danny E., Eichler, Evan E., Mefford, Heather C., Abou‐Khalil, Bassel, Afawi, Zaid Afawi, Allen, Andrew S., Amrom, Dina, Andermann, Eva, Bautista, Jocelyn F., Bellows, Susannah T., Berkovic, Samuel F., Bluvstein, Judith, Boro, Alexis, Burgess, Rosemary, Cascino, Gregory D., Chung, Seo‐Kyung, Consalvo, Damian, Cossette, Patrick, Crompton, Douglas E., Crumrine, Patricia, Curtis, Sarah W., Delanty, Norman, Devinsky, Orrin, Dlugos, Dennis, Ellis, Colin A., Epstein, Michael P., Fiol, Miguel, Fountain, Nathan B., Freyer, Catharine, Friedman, Dan, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gravel, Micheline, Haas, Kevin, Harris, Rebekah V., Haut, Sheryl, Heinzen, Erin L., Helmers, Sandra, Henry, Olivia J., Joshi, Sucheta, Kirsch, Heidi E., Kivity, Sara, Knowlton, Robert C., Kossoff, Eric, Kuzniecky, Ruben, Loeb, Rebecca, Lowenstein, Daniel H., Marson, Anthony G., McCormack, Mark, McGuire, Shannon M., McKenna, Kevin, Motika, Paul V., Mullen, Saul A., Novotny, Edward J., O’Brien, Terence J., Oliver, Karen L., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack M., Park, Kristen L., Paterson, Sarah J., Petrovski, Slave, Pickrell, William O., Poduri, Annapurna, Rees, Mark I., Sadleir, Lynette G., Scheffer, Ingrid E., Shellhaas, Renee A., Sherr, Elliott H., Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K., Sirven, Joseph, Smith, Michael C., Smith, Philip E. M., Sperling, Michael R., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Vining, Eileen P. G., Von Allmen, Gretchen K., Weisenberg, Judith, Widdess‐Walsh, Peter, Winawer, Melodie R.

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Investigating Conceptual Models for the Relationship Between Depression and Condomless Sex Among Gay, Bisexual, and Other Men Who have Sex with Men: Using Structural Equation Model... von Miltz, A. R., Rodger, A. J., Lepri, A. Cozzi, Sewell, J., Nwokolo, N. C., Allan, S., Scott, C., Ivens, D., Lascar, M., Speakman, A., Phillips, A. N., Sherr, L., Collins, S., Elford, J., Lampe, F. C.

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Bayesian Analysis and Design for Joint Modeling of Two Binary Responses With Misclassification von Stamey, James D., Beavers, Daniel P., Sherr, Michael E.

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Effectiveness of Sensor-Augmented Insulin-Pump Therapy in Type 1 Diabetes von Bergenstal, Richard M, Tamborlane, William V, Ahmann, Andrew, Buse, John B, Dailey, George, Davis, Stephen N, Joyce, Carol, Peoples, Tim, Perkins, Bruce A, Welsh, John B, Willi, Steven M, Wood, Michael A

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Assessment, Diagnosis, and Treatment of HIV-Associated Neurocognitive Disorder: A Consensus Report of the Mind Exchange Program von Antinori, A., Arendt, G., Grant, I., Letendre, S., Chair, Munoz-Moreno, J. A., Eggers, C., Brew, B., Brouillette, M.-J., Bernal-Cano, F., Carvalhal, A., Christo, P. P., Cinque, P., Cysique, L., Ellis, R., Everall, I., Gasnault, J., Husstedt, I., Korten, V., Machala, L., Obermann, M., Ouakinin, S., Podzamczer, D., Portegies, P., Rackstraw, S., Rourke, S., Sherr, L., Streinu-Cercel, A., Winston, A., Wojna, V., Yazdanpannah, Y., Arbess, G., Baril, J.-G., Begovac, J., Bergin, C., Bonfanti, P., Bonora, S., Brinkman, K., Canestri, A., Cholewinska-Szymanska, G., Chowers, M., Cooney, J., Corti, M., Doherty, C., Elbirt, D., Esser, S., Florence, E., Force, G., Gill, J., Goffard, J.-C., Harrer, T., Li, P., de Kerckhove, L. V., Knecht, G., Matsushita, S., Matulionyte, R., McConkey, S., Mouglignier, A., Oka, S., Penalva, A., Riesenberg, K., Sambatakou, H., Tozzi, V., Vassallo, M., Wetterberg, P., Drapato, A. W.

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Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study von Stanley, Kate E., Bobbili, Dheeraj R., Dhindsa, Ryan S., May, Patrick, Alldredge, Brian K., Allen, Andrew S., Altmüller, Janine, Amrom, Dina, Andermann, Eva, Auce, Pauls, Avbersek, Andreja, Bautista, Jocelyn F., Becker, Felicitas, Bellows, Susannah T., Berghuis, Bianca, Bluvstein, Judith, Boro, Alex, Burgess, Rosemary, Caglayan, Hande, Cascino, Gregory D., Chung, Seo‐Kyung, Cieuta‐Walti, Cécile, Consalvo, Damian, Cossette, Patrick, Crumrine, Patricia, Delanty, Norman, Depondt, Chantal, Desbiens, Richard, Dlugos, Dennis, Epstein, Michael P., Everett, Kate, Fountain, Nathan B., Francis, Ben, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Girard, Simon, Glauser, Tracy, Glynn, Simon, Gravel, Micheline, Haas, Kevin, Haut, Sheryl R., Heinzen, Erin L., Helbig, Ingo, Hildebrand, Michael S., Jorgensen, Andrea, Joshi, Sucheta, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Kossoff, Eric H., Krause, Roland, Kunz, Wolfram S., Langley, Sarah R., LeGuern, Eric, Lerche, Holger, Leu, Costin, Lortie, Anne, Marson, Anthony G., Mebane, Caroline, Mefford, Heather C., Meloche, Caroline, Motika, Paul V., Muhle, Hiltrud, Nabbout, Rima, Nguyen, Dang K., Nikanorova, Marina, Novotny, Edward J., Ottman, Ruth, O’Brien, Terence J., Paolicchi, Juliann M., Parent, Jack M., Peter, Sarah, Petrou, Steven, Pickrell, William O., Poduri, Annapurna, Radtke, Rodney A., Rees, Mark I., Regan, Brigid M., Sadleir, Lynette G., Sander, Josemir W., Sander, Thomas, Scheffer, Ingrid E., Singh, Rani K., Sirven, Joseph, Sisodiya, Sanjay M., Smith, Michael C., Sonsma, Anja C. M., Sullivan, Joseph, Thio, Liu Lin, Thomas, Rhys H., Venkat, Anu, Von Allmen, Gretchen K., Wang, Quanli, Weber, Yvonne G., Weckhuysen, Sarah, Widdess‐Walsh, Peter, Winawer, Melodie R., Wolking, Stefan, Zimprich, Fritz

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Monoallelic de novo AJAP1 loss-of-function variants disrupt trans-synaptic control of neurotransmitter release von Früh, Simon, Boudkkazi, Sami, Koppensteiner, Peter, Sereikaite, Vita, Chen, Li-Yuan, Fernandez-Fernandez, Diego, Rem, Pascal D, Ulrich, Daniel, Schwenk, Jochen, Chen, Ziyang, Le Monnier, Elodie, Fritzius, Thorsten, Innocenti, Sabrina M, Besseyrias, Valérie, Trovò, Luca, Stawarski, Michal, Argilli, Emanuela, Sherr, Elliott H, van Bon, Bregje, Kamsteeg, Erik-Jan, Iascone, Maria, Pilotta, Alba, Cutrì, Maria R, Azamian, Mahshid S, Hernández-García, Andrés, Lalani, Seema R, Rosenfeld, Jill A, Zhao, Xiaonan, Vogel, Tiphanie P, Ona, Herda, Scott, Daryl A, Scheiffele, Peter, Strømgaard, Kristian, Tafti, Mehdi, Gassmann, Martin, Fakler, Bernd, Shigemoto, Ryuichi, Bettler, Bernhard

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Familial aggregation of status epilepticus in generalized and focal epilepsies von Weisenberg, Judith L.Z., Fitzgerald, Robert T., Constantino, John N., Winawer, Melodie R., Thio, Liu Lin

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