Linear Electromechanical Model of Ionic Polymer Transducers -Part I: Model Development von Newbury, Kenneth M., Leo, Donald J.

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Electromechanical Modeling and Characterization of Ionic Polymer Benders von Newbury, Kenneth M., Leo, Donald J.

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Linear Electromechanical Model of Ionic Polymer Transducers -Part II: Experimental Validation von Newbury, Kenneth M., Leo, Donald J.

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Structural Dynamics of Stiffened Plates with Piezoceramic Sensors and Actuators von Newbury, Kenneth M, Leo, Donald J

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Structural dynamics of stiffened plates with piezoceramic sensors and actuators von Newbury, Kenneth M., Leo, Donald J.

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METHODS AND APPARATAE FOR CONTROLLING AND PROVIDING A VOLTAGE CONVERTER WITH A PULSE-WIDTH-MODULATED SWITCH von NEWBURY, KENNETH M, WILLERS, MICHAEL J, KOWALEWSKI, THOMAS R, WANG, ERYU L

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Method and apparatae for controlling and providing a voltage converter with a pulse-modulated switch von Wang, Eryu L, Newbury, Kenneth M, Willers, Michael J, Kowalewski, Thomas R

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Method and Apparatae for Controlling and Providing a Voltage Converter with a Pulse-Modulated Switch von KOWALEWSKI THOMAS R, WILLERS MICHAEL J, WANG ERYU L, NEWBURY KENNETH M

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METHOD AND APPARATAE FOR CONTROLLING AND PROVIDING A VOLTAGE CONVERTER WITH A PULSE-WIDTH-MODULATED SWITCH von NEWBURY, KENNETH, M, WILLERS, MICHAEL, J, WANG, ERYU, L, KOWALEWSKI, THOMAS, R

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METHODS AND APPARATAE FOR CONTROLLING AND PROVIDING A VOLTAGE CONVERTER WITH A PULSE-WIDTH-MODULATED SWITCH von NEWBURY, KENNETH M, WILLERS, MICHAEL J, KOWALEWSKI, THOMAS R, WANG, ERYU L

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METHOD AND APPARATAE FOR CONTROLLING AND PROVIDING A VOLTAGE CONVERTER WITH A PULSE-WIDTH-MODULATED SWITCH von NEWBURY, KENNETH, M, WILLERS, MICHAEL, J, WANG, ERYU, L, KOWALEWSKI, THOMAS, R

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Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome von Albers, Cornelis A, Paul, Dirk S, Schulze, Harald, Freson, Kathleen, Stephens, Jonathan C, Smethurst, Peter A, Jolley, Jennifer D, Cvejic, Ana, Kostadima, Myrto, Bertone, Paul, Breuning, Martijn H, Debili, Najet, Deloukas, Panos, Favier, Rémi, Fiedler, Janine, Hobbs, Catherine M, Huang, Ni, Hurles, Matthew E, Kiddle, Graham, Krapels, Ingrid, Nurden, Paquita, Ruivenkamp, Claudia A L, Sambrook, Jennifer G, Smith, Kenneth, Stemple, Derek L, Strauss, Gabriele, Thys, Chantal, van Geet, Chris, Newbury-Ecob, Ruth, Ouwehand, Willem H, Ghevaert, Cedric

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Optimizing Making Every Contact Count (MECC) Interventions: A Strategic Behavioral Analysis von Haighton, Catherine, Newbury-Birch, Dorothy, Durlik, Caroline, Sallis, Anna, Chadborn, Tim, Porter, Lucy, Harling, Mandy, Rodrigues, Angela

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GEGEN GEFRIEREN SCHÜTZENDE VERSANDEINHEITEN von SCHEA, III, HENRY, E. 12685 CAMINO MIRA DEL MAR, SAN DIEGO, CA 92130, US, CLEARY, KENNETH, M., JR., NEWBURY PARK, CA 91320, US

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Ultra Low Contact Resistivities for CMOS Beyond 10-nm Node von Zhen Zhang, Koswatta, S. O., Bedell, S. W., Baraskar, A., Guillorn, M., Engelmann, S. U., Yu Zhu, Gonsalves, J., Pyzyna, A., Hopstaken, M., Witt, C., Li Yang, Fei Liu, Newbury, J., Wei Song, Cabral, C., Lofaro, M., Ozcan, A. S., Raymond, M., Lavoie, C., Sleight, J. W., Rodbell, K. P., Solomon, P. M.

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Symptoms Have Modest Accuracy in Detecting Endoscopic and Histologic Remission in Adults With Eosinophilic Esophagitis von Safroneeva, Ekaterina, Straumann, Alex, Coslovsky, Michael, Zwahlen, Marcel, Kuehni, Claudia E, Panczak, Radoslaw, Haas, Nadine A, Alexander, Jeffrey A, Dellon, Evan S, Gonsalves, Nirmala, Hirano, Ikuo, Leung, John, Bussmann, Christian, Collins, Margaret H, Newbury, Robert O, De Petris, Giovanni, Smyrk, Thomas C, Woosley, John T, Yan, Pu, Yang, Guang-Yu, Romero, Yvonne, Katzka, David A, Furuta, Glenn T, Gupta, Sandeep K, Aceves, Seema S, Chehade, Mirna, Spergel, Jonathan M, Schoepfer, Alain M

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Eosinophilic oesophagitis: relationship of quality of life with clinical, endoscopic and histological activity von Safroneeva, E., Coslovsky, M., Kuehni, C. E., Zwahlen, M., Haas, N. A., Panczak, R., Taft, T. H., Hirano, I., Dellon, E. S., Gonsalves, N., Leung, J., Bussmann, C., Woosley, J. T., Yan, P., Romero, Y., Furuta, G. T., Gupta, S. K., Aceves, S. S., Chehade, M., Straumann, A., Schoepfer, A. M., Achem, Sami R., Arora, Amindra S., Alpan, Oral, Alexander, Jeffrey A., Armstrong, David, Attwood, Stephen E., Butterfield, Joseph H., Crowell, Michael D., Petris, Giovanni, DeVault, Kenneth R., Drouin, Eric, Enav, Benjamin, Enders, Felicity T., Fleischer, David E., Foxx‐Orenstein, Amy, Francis, Dawn L., Guyatt, H., Harris, Lucinda A., Kagalwalla, Amir F., Katzka, David A., Kern, Emily, Kita, Hirohito, Krishna, Murli, Lee, James J., Lewis, John C., Lim, Kaiser, Richard Locke, G., Moawad, Fouad J., Murray, oseph A., Nguyen, Cuong C., Newbury, Robert O., Orbelo, Diana M., Pasha, Shabana F., Ramirez, Francisco C., Sheikh, Javed, Smyrk, Thomas C., Spergel, Jonathan M., Umar, Sarah B., Weiler, Catherine R., Wo, John M., Wu, Tsung‐Teh, Yang, Guang‐Yu, Yost, Kathleen J.

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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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Variation in Endoscopic Activity Assessment and Endoscopy Score Validation in Adults With Eosinophilic Esophagitis von Schoepfer, Alain M., Hirano, Ikuo, Coslovsky, Michael, Roumet, Marie C., Zwahlen, Marcel, Kuehni, Claudia E., Hafner, David, Alexander, Jeffrey A., Dellon, Evan S., Gonsalves, Nirmala, Leung, John, Bussmann, Christian, Collins, Margaret H., Newbury, Robert O., Smyrk, Thomas C., Woosley, John T., Yang, Guang-Yu, Romero, Yvonne, Katzka, David A., Furuta, Glenn T., Gupta, Sandeep K., Aceves, Seema S., Chehade, Mirna, Spergel, Jonathan M., Falk, Gary W., Meltzer, Brian A., Comer, Gail M., Straumann, Alex, Safroneeva, Ekaterina, Achem, Sami R., Arora, Amindra S., Alpan, Oral, Armstrong, David, Attwood, Stephen E., Butterfield, Joseph H., Crowell, Michael D., DeVault, Kenneth R., Drouin, Eric, Enav, Benjamin, Enders, Felicity T., Fleischer, David E., Foxx-Orenstein, Amy, Francis, Dawn L., Guyatt, Gordon H., Harris, Lucinda A., Kagalwalla, Amir F., Kita, Hirohito, Krishna, Murli, Lee, James J., Lewis, John C., Lim, Kaiser, Locke, G. Richard, Murray, Joseph A., Nguyen, Cuong C., Orbelo, Diana M., Pasha, Shabana F., Ramirez, Francisco C., Sheikh, Javed, Umar, Sarah B., Weiler, Catherine R., Wo, John M., Wu, Tsung-Teh, Yost, Kathleen J.

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Inheritance of low-frequency regulatory SNPs and a rare null mutation in exon-junction complex subunit RBM8A causes TAR von Albers, Cornelis A, Paul, Dirk S, Schulze, Harald, Freson, Kathleen, Stephens, Jonathan C, Smethurst, Peter A, Jolley, Jennifer D, Cvejic, Ana, Kostadima, Myrto, Bertone, Paul, Breuning, Martijn H, Debili, Najet, Deloukas, Panos, Favier, Rémi, Fiedler, Janine, Hobbs, Catherine M, Huang, Ni, Hurles, Matthew E, Kiddle, Graham, Krapels, Ingrid, Nurden, Paquita, Ruivenkamp, Claudia A L, Sambrook, Jennifer G, Smith, Kenneth, Stemple, Derek L, Strauss, Gabriele, Thys, Chantal, van Geet, Christel, Newbury-Ecob, Ruth, Ouwehand, Willem H, Ghevaert, Cedric

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