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    المصدر: Proceedings of the AAAI Conference on Artificial Intelligence; Vol. 26 No. 1 (2012): Twenty-Sixth AAAI Conference on Artificial Intelligence; 164-170 ; 2374-3468 ; 2159-5399

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    المؤلفون: Moriera, Frederico, So, Kelvin, Gould, Peter, Kamnasaran, Deepak, Jensen, Randy L., Hussain, Ibrahim, Gutmann, David H., Gorovets, Daniel, Kastenhuber, Edward R., Pentsova, Elena, Nayak, Lakshmi, Huse, Jason T., van den Bent, Martin J., Gravendeel, Lonneke A., Gorlia, Thierry, Kros, Johan M., Wesseling, Pieter, Teepen, Johannes, Idbaih, Ahmed, Sanson, Marc, Smitt, Peter A Sillesvis, French, Pim J., Zhang, Wei, Zhang, Jing, Hoadley, Katherine, Carter, Bob, Li, Shouwei, Kang, Chunsheng, You, Yongping, Jiang, Chuanlu, Song, Sonya, Jiang, Tao, Chen, Clark, Grimm, Christiane, Weiler, Markus, Claus, Rainer, Weichenhan, Dieter, Hartmann, Christian, Plass, Christoph, Weller, Michael, Wick, Wolfgang, Jenkins, Robert B., Sicotte, Hugues, Xiao, Yuanyuan, Fridley, Brooke L., Decker, Paul A., Kosel, Matthew L., Kollmeyer, Thomas M., Fink, Stephanie R., Rynearson, Amanda L., Rice, Terri, McCoy, Lucie S., Smirnov, Ivan, Tehan, Tarik, Hansen, Helen M., Patoka, Joseph S., Prados, Michael D., Chang, Susan M., Berger, Mitchel S., Lachance, Daniel H., Wiencke, John K., Wiemels, Joseph L., Wrensch, Margaret R., Gephart, Melanie Hayden, Lee, Eunice, Kyriazopoulou-Panagiotopoulou, Sofia, Milenkovic, Ljiljana, Xun, Xu, Hou, Yong, Kui, Wu, Edwards, Michael, Batzoglou, Serafim, Jun, Wang, Scott, Matthew, Hobbs, Jennifer E., Tipton, Jeremiah, Zhou, Tom, Kelleher, Neil L., Chandler, James P., Schwarzenberg, Johannes, Czernin, Johannes, Cloughesy, Timothy, Ellingson, Benjamin, Geist, Cheri, Phelps, Mike, Chen, Wei, Nakada, Mitsutoshi, Hayashi, Yutaka, Obuchi, Wataru, Ohtsuki, Sumio, Watanabe, Takuya, Ikeda, Chiemi, Misaki, Kouichi, Kita, Daisuke, Hayashi, Yasuhiko, Uchiyama, Naoyuki, Terasaki, Tetsuya, Hamada, Jun-ichiro, Hiddingh, Lotte, Tops, Bastiaan, Hulleman, Esther, Kaspers, Gert-Jan L., Vandertop, W. Peter, Noske, David P., Wurdinger, Tom, Jeuken, Judith W., See, Alfred Pokmeng, Hwang, Taeyoung, Shin, Dongjin, Shin, Joo Heon, Gao, Yuan, Lim, Michael, Hutterer, Markus, Michael, Medinger, Gerold, Untergasser, Karin, Steinlechner, Ingrid, Gstrein, Florian, Deisenhammer, Armin, Muigg, Eugen, Trinka, Eberhard, Gunsilius, Günther, Stockhammer, Cook, Robert W., Oelschlager, Kristen, Sevim, Hatice, Chung, Liping, Wheeler, Helen T., Baxter, Robert C., McDonald, Kerrie L., Chaturbedi, Abhishek, Yu, Liping, Zhou, Yi-Hong, Wong, Anthony, Fatuyi, Remi, Linskey, Mark E., Lavon, Iris, Shahar, Tal, Zrihan, Daniel, Granit, Avital, Ram, Zvi, Siegal, Tali, Brat, Daniel J., Cooper, Lee A., Gutman, David A., Chisolm, Candace S., Appin, Christina, Kong, Jun, Kurc, Tahsin, Van Meir, Erwin G., Saltz, Joel H., Moreno, Carlos S., Abuhusain, Hazem J., Don, Anthony S., Nagarajan, Raman P., Johnson, Brett E., Olshen, Adam B., Xie, Mingchao, Wang, Jiexun, Sundaram, Vasavi, Paris, Pamela, Wang, Ting, Costello, Joseph F., Sijben, Angelique E., Boots-Sprenger, Sandra H., Boogaarts, Jeroen, Rijntjes, Jos, Geitenbeek, Johanna M., van der Palen, Job, Bernsen, Hans J., Schnell, Oliver, Adam, S.A., Eigenbrod, Sabina, Kretzschmar, Hans A., Tonn, Jörg-Christian, Schüller, Ulrich, Sperduto, Paul W., Kased, Norbert, Roberge, David, Xu, Zhiyuan, Shanley, Ryan, Luo, Xianghua, Sneed, Penny K., Chao, Samuel T., Weil, Robert J., Suh, John, Bhatt, Amit, Jensen, Ashley W., Brown, Paul D., Shih, Helen A., Kirkpatrick, John, Gaspar, Laurie E., Fiveash, John B., Chiang, Veronica, Knisely, Jonathan P., Sperduto, Christina M., Lin, Nancy, Mehta, Minesh P., Kwatra, Madan M., Porter, Tara M., Brown, Kristine E., Herndon, James E., Bigner, Darell D., Dahlrot, Rikke H., Kristensen, Bjarne W., Hansen, Steinbjørn, Sulman, Erik P., Cahill, Daniel P., Wang, Meihau, Won, Minhee, Hegi, Monika E., Aldape, Ken D., Gilbert, Mark R., Sadr, Emad Seyed, Tessier, Alain, Sadr, Mohamed Seyed, Alshami, Jad, Sabau, Carmen, Del Maestro, Rolando, Neal, Maxwell L., Rockne, Russell, Trister, Andrew D., Swanson, Kristin R., Maleki, Sanaz, Back, Michael, Buckland, Michael, Brazier, David, McDonald, Kerrie, Cook, Raymond, Parker, Nicole, Wheeler, Helen, Jalbert, Llewellyn, Elkhaled, Adam, Phillips, Joanna J., Yoshihara, Hikari A., Parvataneni, Rupa, Srinivasan, Radhika, Bourne, Gabriela, Cha, Soonmee, Nelson, Sarah J., Aldape, Kenneth D., Gilbert, Mark, Cahill, Daniel, Wang, Meihua, Hegi, Monika, Colman, Howard, Mehta, Minesh, Sulman, Erik, Constantin, Alexandra, Phillips, Joanna, Yoshihara, Hikari, Nelson, Sarah, Gunn, Shelly, Reveles, Xavier T., Tirtorahardjo, Budi, Strecker, Michelle N., Fichtel, Lisa

    مصطلحات موضوعية: Abstracts

    وصف الملف: text/html

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    المصدر: Proceedings of the 57th Annual Meeting of the Association for Computational Linguistics

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    وصف الملف: application/pdf

    Relation: Bohm, Lauren A.; Zhou, Tom C.; Mingo, Tyler J.; Dugan, Sarah L.; Patterson, Richard J.; Sidman, James D.; Roby, Brianne B. (2017). "Neuroradiographic findings in 22q11.2 deletion syndrome." American Journal of Medical Genetics Part A 173(8): 2158-2165.; https://hdl.handle.net/2027.42/137685; American Journal of Medical Genetics Part A; Osborn, R. E., Mojtahedi, S., Hay, T. C., & Dewitt, J. D. ( 1986 ). Internal carotid artery hypoplasia. Computerized Radiology, 10, 283 – 287.; Jalbrzikowski, M., Jonas, R., Senturk, D., Patel, A., Chow, C., Green, M. F., & Bearden, C. E. ( 2013 ). Structural abnormalities in cortical volume, thickness, and surface area in 22q11.2 microdeletion syndrome: Relationship with psychotic symptoms. NeuroImage: Clinical, 3, 405 – 415.; Kates, W. R., Burnette, C. P., Bessette, B. A., Folley, B. S., Strunge, L., Jabs, E. W., & Pearlson, G. D. ( 2004 ). Frontal and caudate alterations in velocardiofacial syndrome (deletion at chromosome 22q11.2). 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Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation. American Journal of Medical Genetics Part A, 140A, 2063 – 2074.; Robin, N. H., & Shprintzen, R. J. ( 2005 ). Defining the clinical spectrum of deletion 22q11.2. Journal of Pediatrics, 147, 90 – 96.; Robin, N. H., Taylor, C. J., McDonald‐McGinn, D. M., Zackai, E. H., Bingham, P., Collins, K. J., … Dobyns, W. B. ( 2006 ). Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation. American Journal of Medical Genetics Part A, 140A, 2416 – 2425.; Ryan, A. K., Goodship, J. A., Wilson, D. I., Philip, N., Levy, A., Seidel, H., … Scambler, P. J. ( 1997 ). Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: A European collaborative study. Journal of Medical Genetics, 34, 798 – 804.; Schaer, M., Glaser, B., Cuadra, M. B., Debbane, M., Thiran, J.‐P., & Eliez, S. ( 2009 ). Congenital heart disease affects local gyrification in 22q11.2 deletion syndrome. Developmental Medicine & Child Neurology, 51, 746 – 753.; Schmitt, J. E., Yi, J. J., Roalf, D. R., Loevner, L. A., Ruparel, K., Whinna, D., … Gur, R. E. ( 2014 ). Incidental radiologic findings in the 22q11.2 deletion syndrome. American Journal of Neuroradiology, 35 ( 11 ), 2186 – 2191.; Shprintzen, R. J. ( 2008 ). Velo‐cardio‐facial syndrome: 30 years of study. Developmental Disabilities Research Reviews, 14, 3 – 10.; Simon, T. J., Ding, L., Bish, J. P., McDonald‐McGinn, D. M., Zackai, E. H., & Gee, J. ( 2005 ). Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: An integrative study. Neuroimage, 25, 169 – 180.; Sprecher, E., Ishida‐Yamamoto, A., Mizrahi‐Koren, M., Rapaport, D., Goldsher, D., Indelman, M., … Mandel, H. ( 2005 ). A mutation in SNAP29, coding for a SNARE protein involved in intracellular trafficking, causes a novel neurocutaneous syndrome characterized by cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma. American Journal of Human Genetics, 77, 242 – 251.; Swillen, A., & McDonald‐McGinn, D. ( 2015 ). Developmental trajectories in 22q11.2 deletion. American Journal of Medical Genetics Part C, 169C ( 2 ), 172 – 181.; Tezenas Du Montcel, S., Mendizabai, H., Ayme, S., Levy, A., & Philip, N. ( 1996 ). Prevalence of 22q11 microdeletion. Journal of Medical Genetics, 33, 719.; Van Amelsvoort, T., Daly, E., Robertson, D., Suckling, J., Ng, V., Critchley, H., … Murphy, D. G. M. ( 2001 ). Structural brain abnormalities associated with deletion at chromosome 22q11: Quantitative neuroimaging study of adults with velo‐cardio‐facial syndrome. British Journal of Psychiatry, 178, 412 – 419.; Vitelli, F., Viola, A., Morishima, M., Pramparo, T., Baldini, A., & Lindsay, E. ( 2003 ). TBX1 is required for inner ear morphogenesis. Human Molecular Genetics, 12, 2041 – 2048.; Andrade, D. M., Krings, T., Chow, E. W., Kiehl, T. R., & Bassett, A. S. ( 2013 ). Hippocampal malrotation is associated with chromosome 22q11.2 microdeletion. Canadian Journal of Neurological Sciences, 40 ( 5 ), 652 – 656.; Barkovich, A. J. ( 2010 ). Current concepts of polymicrogyria. Neuroradiology, 52, 479 – 487.; Barnea‐Goraly, N., Eliez, S., Menon, V., Bammer, R., & Reiss, A. L. ( 2005 ). Arithmetic ability and parietal alterations: A diffusion tensor imaging study in velocardiofacial syndrome. Brain Research. Cognitive Brain Research, 25, 735 – 740.; Bassett, A. S., Chow, E. W. C., Husted, J., Weksberg, R., Caluseriu, O., Webb, G. D., & Gatzoulis, M. A. ( 2005 ). Clinical features of 78 adults with 22q11 deletion syndrome. American Journal of Medical Genetics Part A, 138A, 307 – 313.; Bassett, A. S., McDonald‐McGinn, D. M., Devriendt, K., Digilio, M. C., Goldenberg, P., Habel, A., … Vorstman, J. ( 2011 ). Practical guidelines for managing patients with 22q11.2 deletion syndrome. Journal of Pediatrics, 159, 332 – 339.; Bingham, P. M., Lynch, D., McDonald‐McGinn, D., & Zackai, E. ( 1998 ). Polymicrogyria in chromosome 22 deletion syndrome. Neurology, 51, 1500 – 1502.; Bird, L. M., & Scambler, P. ( 2000 ). Cortical dysgenesis in 2 patients with chromosome 22q11 deletion. Clinical Genetics, 58, 64 – 68.; Bish, J. P., Pendyal, A., Ding, L., Ferrante, H., Nguyen, V., McDonald‐McGinn, D., … Simon, T. J. ( 2006 ). Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome. Neuroscience Letters, 399, 245 – 248.; Campbell, L. E., Daly, E., Toal, F., Stevens, A., Azuma, R., Catani, M., … Murphy, K. C. ( 2006 ). Brain and behaviour in children with 22q11.2 deletion syndrome: A volumetric and voxel‐based morphometry MRI study. Brain, 129, 1218 – 1228.; Chow, E. W. C., Mikulis, D. J., Zipursky, R. B., Scutt, L. E., Weksberg, R., & Bassett, A. S. ( 1999 ). Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia. Biological Psychiatry, 46, 1436 – 1442.; Cioffi, S., Martucciello, S., Fulcoli, F. G., Bilio, M., Ferrentino, R., Nusco, E., & Illingworth, E. ( 2014 ). Tbx1 regulates brain vascularization. Human Molecular Genetics, 23, 78 – 89.; Cramer, S. C., Schaefer, P. W., & Krishnamoorthy, K. S. ( 1996 ). Microgyria in the distribution of the middle cerebral artery in a patient with DiGeorge syndrome. Journal of Child Neurology, 11, 494 – 497.; DeBoer, T., Wu, Z., Lee, A., & Simon, T. J. ( 2007 ). Hippocampal volume reduction in children with chromosome 22q11.2 deletion syndrome is associated with cognitive impairment. Behavioral and Brain Functions, 3, 54.; De Semdt, B., Devriendt, K., Fryns, J. P., Vogels, A., Gewillig, M., & Swillen, A. ( 2007 ). Intellectual abilities in a large sample of children with velo‐cardio‐facial syndrome: An update. Journal of Intellectual Disability Research, 51 ( Pt 9 ), 666 – 670.; Edelmann, L., Pandita, R. K., & Morrow, B. E. ( 1999 ). Low‐copy repeats mediate the common 3‐Mb deletion in patients with velo‐cardio‐facial Syndrome. American Journal of Human Genetics, 64, 1076 – 1086.; Eliez, S., Barnea‐Goraly, N., Schmitt, J. E., Liu, Y., & Reiss, A. L. ( 2002 ). Increased basal ganglia volumes in velo‐cardio‐facial syndrome (deletion 22q11.2). Biological Psychiatry, 52, 68 – 70.; Eliez, S., Schmitt, J. E., White, C. D., & Reiss, A. L. ( 2000 ). Children and adolescents with velocardiofacial syndrome: A volumetric MRI study. American Journal of Psychiatry, 157, 409 – 415.; Emanuel, B. S. ( 2008 ). Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangements. Developmental Disabilities Research Reviews, 14, 11 – 18.; Fung, W. L., Butcher, N. J., Costain, G., Andrade, D. M., Boot, E., Chow, E. W., … Bassett, A. S. ( 2015 ). Practical guidelines for managing adults with 22q11.2 deletion syndrome. Genetics in Medicine, 17 ( 8 ), 599 – 609.; Ghariani, S., Dahan, K., Saint‐Martin, C., Kadhim, H., Morsomme, F., Moniotte, S., … Sébire, G. ( 2002 ). Polymicrogyria in chromosome 22q11 deletion syndrome. European Journal of Paediatric Neurology, 6, 73 – 77.; Goodship, J., Cross, I., LiLing, J., & Wren, C. ( 1998 ). A population study of chromosome 22q11 deletions in infancy. Archives of Disease in Childhood, 79, 348 – 351.; Guerrini, R., & Carrozzo, R. ( 2001 ). Epileptogenic brain malformations: Clinical presentation, malformative patterns and indications for genetic testing. Seizure, 10 ( 7 ), 532 – 543.; Hayashi, N., Tsutsumi, Y., & Barkovich, A. ( 2002 ). Polymicrogyria without porencephaly/schizencephaly. MRI analysis of the spectrum and the prevalence of macroscopic findings in the clinical population. Neuroradiology, 44, 647 – 655.

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