Influence of HLADQA105 Genotype in Adults With Inflammatory Bowel Disease and Anti-TNF Treatment With Proactive Therapeutic Drug Monitoring: A Retrospective Cohort Study von Fuentes-Valenzuela, Esteban, García-Alonso, Francisco Javier, Maroto-Martín, Carlos, Juan Casamayor, Laura, Garrote, José Antonio, Almendros Muñoz, Rosendo, De Prado, Ángel, Vara Castrodeza, Alejando, Marinero, María Ángeles, Calleja Carbajosa, Raquel, Barrio, Jesús

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Esophageal necrosis secondary to thoracic aortic aneurysm von Juan Casamayor, Laura, Martínez Cuevas, Cristina, Fuentes-Valenzuela, Esteban, Alonso-Martín, Carmen

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Esophageal hyperkeratosis as uncommon manifestation of gastroesophageal reflux disease von Sánchez-Delgado, Laura, Fuentes-Valenzuela, Esteban, Burgueño-Gómez, Beatriz, Oyarzún Bahamonde, Elda Paola, Maroto-Martín, Carlos, Fernández-Prada, Samuel, Juan Casamayor, Laura, Moreta-Rodríguez, Miryam

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Esophageal necrosis secondary to thoracic aortic aneurysm: a rare case of dysphagia aortica von Juan Casamayor, Laura, Martínez Cuevas, Cristina, Fuentes-Valenzuela, Esteban, Alonso-Martín, Carmen

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Postreperfusion Biopsy as a Predictor of Biliary Complication After Deceased Donor Liver Transplantation. A Retrospective Cohort Study von Fuentes-Valenzuela, Esteban, Sánchez-Delgado, Laura, Maroto-Martín, Carlos, Juan-Casamayor, Laura, Fernández-Prada, Samuel, Rodríguez, Miryam Moreta, Tejedor-Tejada, Javier, Rubiales, Beatriz Madrigal, Alonso-Martín, Carmen, Peñas-Herrero, Irene, Álvarez, Carolina Almohalla, García-Pajares, Félix

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XI factor deficiency as cause of recurrent gastrointestinal bleeding von Juan-Casamayor, Laura, Fuentes-Valenzuela, Esteban, Alonso-Martín, Carmen, Fernández-Fontecha, Elena, García-Pajares, Félix

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XI factor deficiency as cause of recurrent gastrointestinal bleeding von Juan-Casamayor, Laura, Fernandez-Fontecha, Elena, Fuentes-Valenzuela, Esteban, Garcia-Pajares, Felix, Alonso-Martin, Carmen

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Esophageal hyperkeratosis as an uncommon manifestation of gastroesophageal reflux disease von Moreta-Rodriguez, Miryam, Maroto-Martin, Carlos, Fuentes-Valenzuela, Esteban, Burgueno-Gomez, Beatriz, Bahamonde, Elda Oyarzun, Fernandez-Prada, Samuel, Sanchez-Delgado, Laura, Casamayor, Laura Juan

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Esophageal necrosis secondary to thoracic aortic aneurysm von Juan Casamayor, Laura, Martínez Cuevas, Cristina, Fuentes-Valenzuela, Esteban, Alonso-Martín, Carmen

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XI factor deficiency as cause of recurrent gastrointestinal bleeding von Juan-Casamayor, Laura, Fuentes-Valenzuela, Esteban, Alonso-Martín, Carmen, Fernández-Fontecha, Elena, García-Pajares, Félix

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Esophageal hyperkeratosis as an uncommon manifestation of gastroesophageal reflux disease von Sánchez-Delgado, Laura, Fuentes-Valenzuela, Esteban, Burgueño-Gómez, Beatriz, Oyarzún Bahamonde, Elda Paola, Maroto-Martín, Carlos, Fernández-Prada, Samuel, Juan Casamayor, Laura, Moreta-Rodríguez, Miryam

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New human combined immunodeficiency caused by interferon regulatory factor 4 (IRF4) deficiency inherited by uniparental isodisomy von Bravo García-Morato, María, Aracil Santos, Francisco Javier, Briones, Alejandro Contreras, Blázquez Moreno, Alfonso, del Pozo Maté, Ángela, Domínguez-Soto, Ángeles, Beato Merino, María José, del Pino Molina, Lucía, Torres Canizales, Juan, Marin, Ana Victoria, Vallespín García, Elena, Feito Rodríguez, Marta, Plaza López Sabando, Diego, Jiménez-Reinoso, Anaïs, Mozo del Castillo, Yasmina, Sanz Santaeufemia, Francisco José, de Lucas-Laguna, Raúl, Cárdenas, Paula P., Casamayor Polo, Laura, Coronel Díaz, María, Valés-Gómez, Mar, Roldán Santiago, Ernesto, Ferreira Cerdán, Antonio, Nevado Blanco, Julián, Corbí, Ángel L., Reyburn, Hugh T., Regueiro, José Ramón, López-Granados, Eduardo, Rodríguez Pena, Rebeca

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Conceptual Modeling of Human Genome: Integration Challenges von Pastor, Oscar, Casamayor, Juan Carlos, Celma, Matilde, Mota, Laura, Pastor, M. Ángeles, Levin, Ana M.

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Design and Development of an Information System to Manage Clinical Data about Usher Syndrome Based on Conceptual Modeling von Burriel Coll, Verónica, Pastor Cubillo, Mª Ángeles, Celma Giménez, Matilde, Casamayor Rodenas, Juan Carlos, Mota Herranz, Laura

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New human combined immunodeficiency caused by interferon regulatory factor 4 (IRF4) deficiency inherited by uniparental isodisomy von Bravo García-Morato, María, Aracil Santos, Francisco Javier, Briones, Alejandro Contreras, Blázquez Moreno, Alfonso, Del Pozo Maté, Ángela, Domínguez-Soto, Ángeles, Beato Merino, María José, Del Pino Molina, Lucía, Torres Canizales, Juan, Marin, Ana Victoria, Vallespín García, Elena, Feito Rodríguez, Marta, Plaza López Sabando, Diego, Jiménez-Reinoso, Anaïs, Mozo Del Castillo, Yasmina, Sanz Santaeufemia, Francisco José, de Lucas-Laguna, Raúl, Cárdenas, Paula P, Casamayor Polo, Laura, Coronel Díaz, María, Valés-Gómez, Mar, Roldán Santiago, Ernesto, Ferreira Cerdán, Antonio, Nevado Blanco, Julián, Corbí, Ángel L, Reyburn, Hugh T, Regueiro, José Ramón, López-Granados, Eduardo, Rodríguez Pena, Rebeca

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