The use of intracardiac echocardiography catheters in endocardial ablation of cardiac arrhythmia: Meta‐analysis of efficiency, effectiveness, and safety outcomes von Goya, Masahiko, Frame, Diana, Gache, Larry, Ichishima, Yoko, Tayar, Daiane Oliveira, Goldstein, Laura, Lee, Stephanie Hsiao Yu

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Intracardiac echocardiography use and outcomes after catheter ablation of ventricular tachycardia von Field, Michael E, Goldstein, Laura, Yu Lee, Stephanie Hsiao, Kalsekar, Iftekhar, Coplan, Paul, Wong, Charlene, Khanna, Rahul, Gold, Michael R, Reynolds, Matthew R, Winterfield, Jeffrey R

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Real‐world outcomes of ventricular tachycardia catheter ablation with versus without intracardiac echocardiography von Field, Michael E., Gold, Michael R., Reynolds, Matthew R., Goldstein, Laura, Lee, Stephanie Hsiao Yu, Kalsekar, Iftekhar, Coplan, Paul, Wong, Charlene, Khanna, Rahul, Winterfield, Jeffrey R.

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A real-world analysis of the effectiveness, resource use, and costs associated with ventricular tachycardia catheter ablation in Japanese patients aged ≤75 years von Soejima, Kyoko, Ueda, Akiko, Ogiri, Mami, Ichishima, Yoko, Park, HyeJin, Yu Lee, Stephanie Hsiao

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Health Economic Impact of First Pass Success: An Asia-Pacific Cost Analysis of the ARISE II Study von Yeo, Leonard, Zaidat, Osama O, Saver, Jeffrey L, Mattle, Heinrich P, Lee, Stephanie Hsiao Yu, Kottenmeier, Emilie, Cameron, Heather L, Qadeer, Rana A, Andersson, Tommy

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SYSTEMS AND METHODS FOR TREATMENT OF DEFECTS IN THE VASCULATURE von LEE, Stephanie Hsiao Yu, KOTTENMEIER, Emilie, KHANNA, Rahul

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SYSTEMS AND METHODS FOR TREATMENT OF DEFECTS IN THE VASCULATURE von LEE, Stephanie Hsiao Yu, KOTTENMEIER, Emilie, KHANNA, Rahul

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SYSTEMS AND METHODS FOR TREATMENT OF DEFECTS IN THE VASCULATURE von KOTTENMEIER EMILIE, KHANNA RAHUL, LEE STEPHANIE HSIAO YU

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SYSTEMS AND METHODS FOR TREATMENT OF DEFECTS IN VASCULATURE von RAHUL KHANNA, STEPHANIE HSIAO YU LEE, EMILIE KOTTENMEIER

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DECOMPENSATED HEART FAILURE DUE TO NEW DIAGNOSIS OF WPW IN AN ELDERLY WOMAN von Moser, Hannah, Hsiao, Stephanie, Tsai, Stacy, Yee, Rupsa, Lee, Chun-Yu, Hongo, Richard

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De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia von Kanca, Oguz, Andrews, Jonathan C., Patel, Chirag, Slavotinek, Anne M., Williams, Judy, Indaram, Maanasa, Lau, C. Christopher, Adams, David R., Agrawal, Pankaj, Bademci, Guney, Baker, Eva, Baldridge, Dustin, Bale, Jim, Batzli, Gabriel F., Bayrak-Toydemir, Pinar, Bernstein, Jonathan A., Bick, David P., Bohnsack, John, Briere, Lauren C., Carey, John, Cogan, Joy D., Cole, F. Sessions, D'Souza, Precilla, Dayal, Jyoti G., Dorset, Daniel C., Douine, Emilie D., Draper, David D., Duncan, Laura, Fieg, Elizabeth L., Forghani, Irman, Fresard, Laure, Godfrey, Rena A., Goldman, Alica M., Groden, Catherine A., Haendel, Melissa, Hayes, Nichole, Huang, Alden, Huang, Yong, Jones, Angela L., Krasnewich, Donna M., Kyle, Jennifer E., Lalani, Seema R., Lau, C. Christopher, Levy, Shawn E., Liu, Xue Zhong, Loo, Sandra K., Loscalzo, Joseph, Markello, Thomas C., Marth, Gabor, McConkie-Rosell, Allyn, Might, Matthew, Morimoto, Marie, Nelson, Stan F., Newberry, J. Scott, Newman, John H., Orengo, James P., Pak, Stephen, Pallais, J. Carl, Palmer, Christina G.S., Papp, Jeanette C., Parker, Neil H., Pusey, Barbara N., Quinlan, Aaron, Raja, Archana N., Rosenfeld, Jill A., Ruzhnikov, Maura, Samson, Susan L., Schaechter, Judy, Schedl, Timothy, Schoch, Kelly, Shakachite, Lisa, Sharma, Prashant, Shashi, Vandana, Shields, Kathleen, Sillari, Catherine H., Sinsheimer, Janet S., Smith, Kevin S., Solnica-Krezel, Lilianna, Spillmann, Rebecca C., Stong, Nicholas, Sweetser, David A., Tekin, Mustafa, Telischi, Fred, Tran, Alyssa A., Urv, Tiina K., Vogel, Tiphanie P., Wahl, Colleen E., Walley, Nicole M., Wang, Lee-kai, Wangler, Michael F., Wegner, Daniel, Wolfe, Lynne A., Worthey, Elizabeth A., Yu, Guoyun, Zhao, Chunli, Chung, Wendy K., Dobyns, William B., Adams, David R., Gahl, William A., Malicdan, May Christine V.

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Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder von Schneeberger, Pauline E, Kortüm, Fanny, Korenke, Georg Christoph, Alawi, Malik, Santer, René, Woidy, Mathias, Buhas, Daniela, Fox, Stephanie, Juusola, Jane, Alfadhel, Majid, Webb, Bryn D, Coci, Emanuele G, Abou Jamra, Rami, Siekmeyer, Manuela, Biskup, Saskia, Heller, Corina, Maier, Esther M, Javaher-Haghighi, Poupak, Bedeschi, Maria F, Ajmone, Paola F, Iascone, Maria, Peeters, Hilde, Ballon, Katleen, Jaeken, Jaak, Rodríguez Alonso, Aroa, Palomares-Bralo, María, Santos-Simarro, Fernando, Meuwissen, Marije E C, Beysen, Diane, Kooy, R Frank, Houlden, Henry, Murphy, David, Doosti, Mohammad, Karimiani, Ehsan G, Mojarrad, Majid, Maroofian, Reza, Noskova, Lenka, Kmoch, Stanislav, Honzik, Tomas, Cope, Heidi, Sanchez-Valle, Amarilis, Gelb, Bruce D, Kurth, Ingo, Hempel, Maja, Kutsche, Kerstin

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Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain von Erger, Florian, Settas, Nikolaos, London, Edra, Torti, Erin, Nelson, Stanley F., Acosta, Maria T., Adams, David R., Balasubramanyam, Ashok, Baldridge, Dustin, Bale, Jim, Bamshad, Michael, Bayrak-Toydemir, Pinar, Beck, Anita, Bennett, Jimmy, Bernstein, Jonathan A., Blue, Elizabeth, Bohnsack, John, Bonnenmann, Carsten, Boyd, Brenna, Brokamp, Elly, Burke, Elizabeth A., Byrd, William E., Carrasquillo, Olveen, Chanprasert, Sirisak, Chao, Hsiao-Tuan, Coggins, Matthew, Cole, F. Sessions, Crouse, Andrew B., Cunningham, Michael, D’Souza, Precilla, Dai, Hongzheng, Dipple, Katrina, Doherty, Daniel, Earl, Dawn, Eckstein, David J., Eng, Christine M., Ferreira, Carlos, Glass, Ian, Gochuico, Bernadette, Goldman, Alica M., Goldstein, David B., Hassey, Kelly, Hom, Jason, Huang, Yong, Jarvik, Gail P., Jarvik, Jeffrey, Krasnewich, Donna M., LaMoure, Grace L., Lalani, Seema R., Lanpher, Brendan C., Latham, Lea, Liu, Pengfei, Liu, Xue Zhong, Macnamara, Ellen F., Malicdan, May Christine V., Manolio, Teri A., Maravilla, Kenneth, Marom, Ronit, Martin, Beth A., Marwaha, Shruti, McCormack, Colleen E., McGee, Elisabeth, Might, Matthew, Nakano-Okuno, Mariko, Nath, Avi, Nicholas, Sarah K., Novacic, Donna, Orengo, James P., Pallais, J. Carl, Palmer, Christina G.S., Parker, Neil H., Posey, Jennifer E., Quinlan, Aaron, Reuter, Chloe M., Robertson, Amy K., Ruzhnikov, Maura, Samson, Susan L., Saporta, Mario, Schaechter, Judy, Signer, Rebecca H., Smith, Kevin S., Ben Solomon, Stoler, Joan M., Sullivan, Jennifer A., Sullivan, Kathleen, Sun, Angela, Tabor, Holly K., Tucker, Brianna M., Vanderver, Adeline, Wallace, Stephanie, Wangler, Michael F., Ward, Patricia A., Whitlock, Jordan, Wolfe, Lynne A., Woods, Jeremy D., Zastrow, Diane B., Grange, Dorothy K., Willaert, Rebecca, Theiß, Susanne, Stocco, Amber

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De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia von Patel, Chirag, Cohen, Julie S., Gubbels, Cynthia S., Aldinger, Kimberly A., Crawford, Joanna, Adams, David R., Agrawal, Pankaj, Bademci, Guney, Baker, Eva, Baldridge, Dustin, Bale, Jim, Batzli, Gabriel F., Bayrak-Toydemir, Pinar, Bernstein, Jonathan A., Bick, David P., Bohnsack, John, Briere, Lauren C., Carey, John, Cogan, Joy D., Cole, F. Sessions, Cooper, Cynthia M., D'Souza, Precilla, Dayal, Jyoti G., Dell'Angelica, Esteban C., Dorset, Daniel C., Douine, Emilie D., Draper, David D., Duncan, Laura, Fieg, Elizabeth L., Forghani, Irman, Fresard, Laure, Godfrey, Rena A., Goldman, Alica M., Groden, Catherine A., Haendel, Melissa, Hayes, Nichole, Huang, Alden, Huang, Yong, Jones, Angela L., Krasnewich, Donna M., Kyle, Jennifer E., Lalani, Seema R., Lazar, Jozef, Lee, Hane, Levy, Shawn E., Lincoln, Sharyn A., Liu, Xue Zhong, Loo, Sandra K., Loscalzo, Joseph, Markello, Thomas C., Marth, Gabor, Marwaha, Shruti, McConkie-Rosell, Allyn, Might, Matthew, Morimoto, Marie, Murdock, David R., Nelson, Stan F., Newberry, J. Scott, Newman, John H., Orengo, James P., Pak, Stephen, Pallais, J. Carl, Palmer, Christina G.S., Papp, Jeanette C., Parker, Neil H., Pusey, Barbara N., Quinlan, Aaron, Raja, Archana N., Rosenfeld, Jill A., Ruzhnikov, Maura, Samson, Susan L., Schaechter, Judy, Schedl, Timothy, Schoch, Kelly, Shakachite, Lisa, Sharma, Prashant, Shashi, Vandana, Shields, Kathleen, Sillari, Catherine H., Sinsheimer, Janet S., Smith, Kevin S., Solnica-Krezel, Lilianna, Spillmann, Rebecca C., Stong, Nicholas, Sweetser, David A., Tekin, Mustafa, Telischi, Fred, Tran, Alyssa A., Urv, Tiina K., Vogel, Tiphanie P., Wahl, Colleen E., Walley, Nicole M., Wang, Lee-kai, Wangler, Michael F., Wegner, Daniel, Wolfe, Lynne A., Worthey, Elizabeth A., Yu, Guoyun, Zhao, Chunli, Malicdan, May Christine V.

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Progenitor Cells Derived from Drain Waste Product of Open-Heart Surgery in Children von Wong, Tak-Wah, Kan, Chung-Dann, Chiu, Wen-Tai, Fok, Kin Lam, Ruan, Ye Chun, Jiang, Xiaohua, Chen, Junjiang, Kao, Chiu-Ching, Chen, I-Yu, Lin, Hui-Chun, Chou, Chia-Hsuan, Lin, Chou-Wen, Yu, Chun-Keung, Tsao, Stephanie, Lee, Yi-Ping, Chan, Hsiao Chang, Wang, Jieh-Neng

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Abstract 798: SeroNet Pooling Project of immunocompromised populations von Kazemain, Elham, Figueiredo, Jane, Skarbinski, Jacek, McBride, Russell, Simon, Viviana, Karger, Amy B., Lee, F. Eun-Hyung, Hirsch, Fred R., Cox, Andrea, Klein, Sabra, Fan, Rong, Halene, Stephanie, Zidar, David A., Crawford, James M., Thyagarajan, Bharat, Gleason, Charles, Mathson, Alex, Srivastava, Komal, Moshele, Puleng, Amoss, Toby, Runnstrom, Martin, Linderman, Susanne, Rodilla, Ananda M., Mack, Philip C., Shyr, Yu, Yin, Anna, Shea, Patrick, VanOudenhove, Jennifer, Siddiqui, Hinnah, Wilson, Brigid M., Elkin, Eric P., Hsiao, Crystal A., Ziemba, Yonah, Schleicher, Cheryl B., Fox, Sharon, Kushi, Lawrence H., Reckamp, Karen, Merchant, Akil, Merin, Noah

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Analysis of Heritability and Shared Heritability Based on Genome-Wide Association Studies for Thirteen Cancer Types von Sampson, Joshua N, Panagiotou, Orestis, Wang, Zhaoming, Albanes, Demetrius, An, She-Juan, Armstrong, Bruce K, Barkauskas, Donald A, Benhamou, Simone, Berg, Christine, Birmann, Brenda M, Burdett, Laurie, Carreon, Tania, Chen, Chu, Chen, Kun-Chieh, Choi, Jin Eun, Clavel-Chapelon, Françoise, Cocco, Pierluigi, Cortessis, Victoria K, Cozen, Wendy, Feychting, Maria, Flanagan, Adrienne M, Foretova, Lenka, Fuchs, Charles, Gapstur, Susan M, Garcia-Closas, Montserrat, Gaziano, J Michael, Glimelius, Bengt, Goldstein, Alisa M, Gunter, Marc, Guo, Huan, He, Xingzhou, Henderson, Brian, Hosain, G M Monawar, Huerta, Jose-Maria, Johansen, Christoffer, Karagas, Margaret R, Kim, Christopher, Kim, Yeul Hong, Kim, Young Tae, Klein, Robert J, Krogh, Vittorio, Kunitoh, Hideo, LaCroix, Andrea, Lawrence, Charles, Lecanda, Fernando, Li, Donghui, Li, Jihua, Li, Yuqing, Liao, Linda M, Liebow, Mark, Lin, Chien-Chung, Lu, Daru, Lund, Eiluv, Michaud, Dominique S, Monnereau, Alain, Mortensen, Lotte Maxild, Nieters, Alexandra, North, Kari E, Peeters, Petra H M, Peters, Ulrike, Petersen, Gloria M, Qiao, You-Lin, Riby, Jacques, Seow, Adeline, Serra, Consol, Serra, Massimo, Shen, Hongbing, Sihoe, Alan Dart Loon, Smith, Alex, Sund, Malin, Sung, Sook Whan, Tang, Wei, Trichopoulos, Dimitrios, Tucker, Margaret, Turner, Jenny, Vineis, Paolo, Virtamo, Jarmo, Wactawski-Wende, Jean, Wang, Chaoyu, Weiderpass, Elisabete, Wentzensen, Nicolas, Witzig, Thomas E, Wu, Chen, Wu, Junjie, Wu, Yi-Long, Xiang, Yong-Bing, Yoon, Ho-Il, Yu, Chong-Jen, Zhang, Xu-Chao, Zheng, Tongzhang, Zheng, Wei, Cerhan, James R, Magnani, Corrado, Vijai, Joseph, Wang, Sophia S, Hunter, David J, Silverman, Debra T, Slager, Susan L, Chanock, Stephen J, Chatterjee, Nilanjan

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