Concurrent MEK2 Mutation and BRAF Amplification Confer Resistance to BRAF and MEK Inhibitors in Melanoma
Villanueva, Jessie, Infante, Jeffrey R., Krepler, Clemens, Reyes-Uribe, Patricia, Samanta, Minu, Chen, Hsin-Yi, Li, Bin, Swoboda, Rolf K., Wilson, Melissa, Vultur, Adina, Fukunaba-Kalabis, Mizuho, Wubbenhorst, Bradley, Chen, Thomas Y., Liu, Qin, Sproesser, Katrin, DeMarini, Douglas J., Gilmer, Tona M., Martin, Anne-Marie, Marmorstein, Ronen, Schultz, David C., Speicher, David W., Karakousis, Giorgos C., Xu, Wei, Amaravadi, Ravi K., Xu, Xiaowei, Schuchter, Lynn M., Herlyn, Meenhard, Nathanson, Katherine L.
Published in Cell reports (Cambridge) (26.09.2013)
Published in Cell reports (Cambridge) (26.09.2013)
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The association between electronic health information usage and patient-centered communication: a cross sectional analysis from the Health Information National Trends Survey (HINTS)
Knowles, Heidi, Swoboda, Thomas K, Sandlin, Devin, Huggins, Charles, Takami, Trevor, Johnson, Garrett, Wang, Hao
Published in BMC health services research (12.12.2023)
Published in BMC health services research (12.12.2023)
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Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria
Bruno, M K, Hallett, M, Gwinn-Hardy, K, Sorensen, B, Considine, E, Tucker, S, Lynch, D R, Mathews, K D, Swoboda, K J, Harris, J, Soong, B W, Ashizawa, T, Jankovic, J, Renner, D, Fu, Y H, Ptacek, L J
Published in Neurology (28.12.2004)
Published in Neurology (28.12.2004)
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An integrated expression atlas of miRNAs and their promoters in human and mouse
de Rie, Derek, Abugessaisa, Imad, Alam, Tanvir, Arner, Erik, Arner, Peter, Ashoor, Haitham, Åström, Gaby, Babina, Magda, Bertin, Nicolas, Burroughs, A Maxwell, Carlisle, Ailsa J, Daub, Carsten O, Detmar, Michael, Deviatiiarov, Ruslan, Fort, Alexandre, Gebhard, Claudia, Goldowitz, Daniel, Guhl, Sven, Ha, Thomas J, Harshbarger, Jayson, Hasegawa, Akira, Hashimoto, Kosuke, Herlyn, Meenhard, Heutink, Peter, Hitchens, Kelly J, Hon, Chung Chau, Huang, Edward, Ishizu, Yuri, Kai, Chieko, Kasukawa, Takeya, Klinken, Peter, Lassmann, Timo, Lecellier, Charles-Henri, Lee, Weonju, Lizio, Marina, Makeev, Vsevolod, Mathelier, Anthony, Medvedeva, Yulia A, Mejhert, Niklas, Mungall, Christopher J, Noma, Shohei, Ohshima, Mitsuhiro, Okada-Hatakeyama, Mariko, Persson, Helena, Rizzu, Patrizia, Roudnicky, Filip, Sætrom, Pål, Sato, Hiroki, Severin, Jessica, Shin, Jay W, Swoboda, Rolf K, Tarui, Hiroshi, Toyoda, Hiroo, Vitting-Seerup, Kristoffer, Winteringham, Louise, Yamaguchi, Yoko, Yasuzawa, Kayoko, Yoneda, Misako, Yumoto, Noriko, Zabierowski, Susan, Zhang, Peter G, Wells, Christine A, Summers, Kim M, Kawaji, Hideya, Sandelin, Albin, Rehli, Michael, Hayashizaki, Yoshihide, Carninci, Piero, Forrest, Alistair R R, de Hoon, Michiel J L
Published in Nature biotechnology (01.09.2017)
Published in Nature biotechnology (01.09.2017)
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The Children’s Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND): Test development and reliability
Glanzman, A.M, Mazzone, E, Main, M, Pelliccioni, M, Wood, J, Swoboda, K.J, Scott, C, Pane, M, Messina, S, Bertini, E, Mercuri, E, Finkel, R.S
Published in Neuromuscular disorders : NMD (01.03.2010)
Published in Neuromuscular disorders : NMD (01.03.2010)
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Favorably skewed X-inactivation accounts for neurological sparing in female carriers of Menkes disease
Desai, V, Donsante, A, Swoboda, KJ, Martensen, M, Thompson, J, Kaler, SG
Published in Clinical genetics (01.02.2011)
Published in Clinical genetics (01.02.2011)
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Journal Article
Assessing Interpersonal and Communication Skills in Emergency Medicine
Chan, Teresa M., Wallner, Clare, Swoboda, Thomas K., Leone, Katrina A., Kessler, Chad
Published in Academic emergency medicine (01.12.2012)
Published in Academic emergency medicine (01.12.2012)
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Journal Article
Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy
Wattanasirichaigoon, D, Swoboda, K J, Takada, F, Tong, H-Q, Lip, V, Iannaccone, S T, Wallgren-Pettersson, C, Laing, N G, Beggs, A H
Published in Neurology (27.08.2002)
Published in Neurology (27.08.2002)
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Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy
Lampe, A K, Dunn, D M, von Niederhausern, A C, Hamil, C, Aoyagi, A, Laval, S H, Marie, S K, Chu, M-L, Swoboda, K, Muntoni, F, Bonnemann, C G, Flanigan, K M, Bushby, K M D, Weiss, R B
Published in Journal of medical genetics (01.02.2005)
Published in Journal of medical genetics (01.02.2005)
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Using natural language processing in emergency medicine health service research: A systematic review and meta‐analysis
Wang, Hao, Alanis, Naomi, Haygood, Laura, Swoboda, Thomas K., Hoot, Nathan, Phillips, Daniel, Knowles, Heidi, Stinson, Sara Ann, Mehta, Prachi, Sambamoorthi, Usha
Published in Academic emergency medicine (01.07.2024)
Published in Academic emergency medicine (01.07.2024)
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Journal Article
G.O.18
Darras, B, Chiriboga, C, Swoboda, K, Iannaccone, S, Montes, J, Castro, D, Holuba, N, Raush, N, Visyak, N, Dunaway, S, Trussell, D, Pasternak, A, Neilson, L, Vivo, D. De, McGuire, D, Norris, D, Alexander, K, Bennett, C.F, Bishop, K
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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Preclinical validation of a multiplex real-time assay to quantify SMN mRNA in patients with SMA
Simard, L R, Bélanger, M-C, Morissette, S, Wride, M, Prior, T W, Swoboda, K J
Published in Neurology (06.02.2007)
Published in Neurology (06.02.2007)
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O.9 First-in-human phase I study to assess safety, tolerability and dose for intrathecal injection of ISIS-SMNRx in SMA patients
Swoboda, K, Chiriboga, C, Darras, B, Iannaccone, S, Montes, J, Rausch, N, Parad, R, Johnson, S, Vivo, D. De, Norris, D, Alexander, K, Bennet, F.C, Bishop, K
Published in Neuromuscular disorders : NMD (01.10.2013)
Published in Neuromuscular disorders : NMD (01.10.2013)
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Journal Article
P1.12 Frequency of genomic deletion mutations in collagen VI myopathies
Butterfield, R.J, Swoboda, K, Flanigan, K.M, Bonnemann, C.G, Weiss, R.B
Published in Neuromuscular disorders : NMD (01.10.2010)
Published in Neuromuscular disorders : NMD (01.10.2010)
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134th ENMC International Workshop: Outcome Measures and Treatment of Spinal Muscular Atrophy, 11-13 February 2005, Naarden, The Netherlands
Bertini, E, Burghes, A, Bushby, K, Estournet-Mathiaud, B, Finkel, R S, Hughes, R A C, Iannaccone, S T, Melki, J, Mercuri, E, Muntoni, F, Voit, T, Reitter, B, Swoboda, K J, Tiziano, D, Tizzano, E, Topaloglu, H, Wirth, B, Zerres, K
Published in Neuromuscular disorders : NMD (01.11.2005)
Published in Neuromuscular disorders : NMD (01.11.2005)
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Journal Article
Conference Proceeding
Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies
Swoboda, K J, Soong, B, McKenna, C, Brunt, E R, Litt, M, Bale, Jr, J F, Ashizawa, T, Bennett, L B, Bowcock, A M, Roach, E S, Gerson, D, Matsuura, T, Heydemann, P T, Nespeca, M P, Jankovic, J, Leppert, M, Ptácek, L J
Published in Neurology (25.07.2000)
Published in Neurology (25.07.2000)
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