Výsledky vyhledávání - Vega, Hugo

Association of Allelic Variants of the Reelin Gene with Autistic Spectrum Disorder: A Systematic Review and Meta-Analysis of Candidate Gene Association Studies Autor Hernández-García, Ignacio, Chamorro, Antonio-Javier, Ternavasio-de la Vega, Hugo Guillermo, Carbonell, Cristina, Marcos, Miguel, Mirón-Canelo, José-Antonio

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Therapeutic and Preventive Efficacy of an Intervention on Workers in a Back School Autor Rodríguez, Alberto Benito, Ternavasio-de la Vega, Hugo Guillermo, Santos Sánchez, José Ángel, Iglesias de Sena, Helena, Marcos, Miguel, Chamorro, Antonio Javier, Mirón-Canelo, José Antonio

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Skin and Soft Tissue Infections (Patera Foot) in Immigrants, Spain Autor Ternavasio-de la Vega, Hugo-Guillermo, Ángel-Moreno, Alfonso, Hernández-Cabrera, Michele, Pisos-Álamo, Elena, Bolaños-Rivero, Margarita, Carranza-Rodriguez, Cristina, Calderín-Ortega, Antonio, Pérez-Arellano, José-Luis

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A Propensity Score Analysis Shows that Empirical Treatment with Linezolid Does Not Increase the Thirty-Day Mortality Rate in Patients with Gram-Negative Bacteremia Autor Ternavasio-de la Vega, Hugo-Guillermo, Mateos-Díaz, Ana-María, Martinez, Jose-Antonio, Almela, Manel, Cobos-Trigueros, Nazaret, Morata, Laura, De-la-Calle, Cristina, Sala, Marta, Mensa, Josep, Marcos, Miguel, Soriano, Alex

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Transcriptional Dysregulation in NIPBL and Cohesin Mutant Human Cells Autor Liu, Jinglan, Zhang, Zhe, Bando, Masashige, Itoh, Takehiko, Deardorff, Matthew A., Clark, Dinah, Kaur, Maninder, Tandy, Stephany, Kondoh, Tatsuro, Rappaport, Eric, Spinner, Nancy B., Vega, Hugo, Jackson, Laird G., Shirahige, Katsuhiko, Krantz, Ian D.

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Genome-wide DNA methylation analysis in cohesin mutant human cell lines Autor Liu, Jinglan, Zhang, Zhe, Bando, Masashige, Itoh, Takehiko, Deardorff, Matthew A., Li, Jennifer R., Clark, Dinah, Kaur, Maninder, Tatsuro, Kondo, Kline, Antonie D., Chang, Celia, Vega, Hugo, Jackson, Laird G., Spinner, Nancy B., Shirahige, Katsuhiko, Krantz, Ian D.

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ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13 Autor Zhang, Yihan, Huang, Haigen, Zhao, Gexin, Yokoyama, Tadafumi, Vega, Hugo, Huang, Yan, Sood, Raman, Bishop, Kevin, Maduro, Valerie, Accardi, John, Toro, Camilo, Boerkoel, Cornelius F., Lyons, Karen, Gahl, William A., Duan, Xiaohong, Malicdan, May Christine V., Lin, Shuo

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Correction: ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13 Autor Zhang, Yihan, Huang, Haigen, Zhao, Gexin, Yokoyama, Tadafumi, Vega, Hugo, Huang, Yan, Sood, Raman, Bishop, Kevin, Maduro, Valerie, Accardi, John, Toro, Camilo, Boerkoel, Cornelius F., Lyons, Karen, Gahl, William A., Duan, Xiaohong, Malicdan, May Christine V., Lin, Shuo

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Three Rare Diseases in One Sib Pair: RAI1, PCK1, GRIN2B Mutations Associated with Smith-Magenis Syndrome, Cytosolic PEPCK Deficiency and NMDA Receptor Glutamate Insensitivity Autor Adams, David R, Yuan, Hongjie, Holyoak, Todd, Arajs, Katrina H., Hakimi, Parvin, Markello, Thomas C, Wolfe, Lynne A, Vilboux, Thierry, Burton, Barbara K, Fajardo, Karin Fuentes, Grahame, George, Holloman, Conisha, Sincan, Murat, Smith, Ann C M, Wells, Gordon A, Huang, Yan, Vega, Hugo, Snyder, James P, Golas, Gretchen A, Tifft, Cynthia J, Boerkoel, Cornelius F, Hanson, Richard W, Traynelis, Stephen F, Kerr, Douglas S, Gahl, William A

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Glycosylation, Hypogammaglobulinemia, and Resistance to Viral Infections Autor Sadat, Mohammed A., Moir, Susan, Chun, Tae-Wook, Lusso, Paolo, Kaplan, Gerardo, Wolfe, Lynne, Memoli, Matthew J., He, Miao, Vega, Hugo, Kim, Leo J.Y., Huang, Yan, Hussein, Nadia, Nievas, Elma, Mitchell, Raquel, Garofalo, Mary, Louie, Aaron, Ireland, Derek C., Grunes, Claire, Cimbro, Raffaello, Patel, Vyomesh, Holzapfel, Genevieve, Salahuddin, Daniel, Bristol, Tyler, Adams, David, Marciano, Beatriz E., Hegde, Madhuri, Li, Yuxing, Calvo, Katherine R., Stoddard, Jennifer, Justement, J. Shawn, Jacques, Jerome, Priel, Debra A. Long, Murray, Danielle, Sun, Peter, Kuhns, Douglas B., Boerkoel, Cornelius F., Chiorini, John A., Di Pasquale, Giovanni, Verthelyi, Daniela, Rosenzweig, Sergio D.

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