The genetics of celiac disease: A comprehensive review of clinical implications von Dieli-Crimi, Romina, Cénit, M. Carmen, Núñez, Concepción

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Inflammatory bowel disease and celiac disease:Overlaps and differences von Pascual, Virginia, Dieli-Crimi, Romina, López-Palacios, Natalia, Bodas, Andrés, Medrano, Luz María, Núñez, Concepción

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Primary and Secondary Immunodeficiency Diseases in Oncohaematology: Warning Signs, Diagnosis, and Management von Sánchez-Ramón, Silvia, Bermúdez, Arancha, González-Granado, Luis Ignacio, Rodríguez-Gallego, Carlos, Sastre, Ana, Soler-Palacín, Pere

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Coordinated Response to Imported Vaccine-Derived Poliovirus Infection, Barcelona, Spain, 2019-2020 von Álamo-Junquera, Dolores, Politi, Julieta, Simón, Pere, Dieli-Crimi, Romina, Borrell, Ricardo Pujol, Colobran, Roger, Martínez-Gallo, Monica, Campins, Magda, Antón, Andrés, Esperalba, Juliana, Andrés, Cristina, Codina, María Gema, Polverino, Eva, Narciso, M Rosa, Molinero, Emilia, Rius, Cristina

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Common Variable Immunodeficiency and Neurodevelopmental Delay Due to a 13Mb Deletion on Chromosome 4 Including the NFKB1 Gene: A Case Report von Franco-Jarava, Clara, Valenzuela, Irene, Riviere, Jacques G., Garcia-Prat, Marina, Martínez-Gallo, Mónica, Dieli-Crimi, Romina, Castells, Neus, Batlle-Masó, Laura, Soler-Palacin, Pere, Colobran, Roger

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A Polymorphism Within the MBP Gene Is Associated With a Higher Relapse Number in Male Patients of Multiple Sclerosis von Espino-Paisán, Laura, Agudo-Jiménez, Teresa, Rosales-Martínez, Isabel, López-Cotarelo, Pilar, García-Martínez, María Ángel, Domínguez-Mozo, María Inmaculada, Pérez-Pérez, Silvia, Dieli-Crimi, Romina, Comabella, Manuel, Urcelay, Elena, Álvarez-Lafuente, Roberto

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An autoimmune polyglandular syndrome complicated with celiac disease and autoimmune hepatitis von Dieli-Crimi, Romina, Núñez, Concepción, Estrada, Lourdes, López-Palacios, Natalia

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OTULIN Haploinsufficiency Causes Hyperinflammatory Responses to Infectious and Non-Infectious Triggers von Batlle-Masó, Laura, Antolin, Maria, Marques-Soares, Joana, Dieli-Crimi, Romina, Colobran, Roger

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The kappa free light chain index and oligoclonal bands have a similar role in the McDonald criteria von Arrambide, Georgina, Espejo, Carmen, Carbonell-Mirabent, Pere, Dieli-Crimi, Romina, Rodríguez-Barranco, Marta, Castillo, Mireia, Auger, Cristina, Cárdenas-Robledo, Simón, Castilló, Joaquín, Cobo-Calvo, Álvaro, Galán, Ingrid, Midaglia, Luciana, Nos, Carlos, Otero-Romero, Susana, Río, Jordi, Rodríguez-Acevedo, Breogán, Ruiz-Ortiz, Mariano, Salerno, Annalaura, Tagliani, Paula, Tur, Carmen, Vidal-Jordana, Angela, Zabalza, Ana, Sastre-Garriga, Jaume, Rovira, Alex, Comabella, Manuel, Hernández-González, Manuel, Montalban, Xavier, Tintore, Mar

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Development of an Expert-Based Scoring System for Early Identification of Patients with Inborn Errors of Immunity in Primary Care Settings – the PIDCAP Project von Rivière, Jacques G., Carot-Sans, Gerard, Piera-Jiménez, Jordi, de la Torre, Sergi, Cos, Xavier, Serra-Picamal, Xavier, Soler-Palacin, Pere

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Heterozygous Predicted Loss-of-function Variants of TRAF3 in Patients with Common Variable Immunodeficiency von Urban, Blanca, Batlle-Masó, Laura, Perurena-Prieto, Janire, Garcia-Prat, Marina, Parra-Martínez, Alba, Aguiló-Cucurull, Aina, Martinez-Gallo, Mónica, Moushib, Laith, Antolín, María, Rivière, Jacques G., Soler-Palacin, Pere, Dieli-Crimi, Romina, Franco-Jarava, Clara, Colobran, Roger

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Role of Skewed X-Chromosome Inactivation in Common Variable Immunodeficiency von Garcia-Prat, Marina, Batlle-Masó, Laura, Parra-Martínez, Alba, Franco-Jarava, Clara, Martinez-Gallo, Mónica, Aguiló-Cucurull, Aina, Perurena-Prieto, Janire, Castells, Neus, Urban, Blanca, Dieli-Crimi, Romina, Soler-Palacín, Pere, Colobran, Roger

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Serum protein electrophoresis and complement deficiencies: a veteran but very versatile test in clinical laboratories von Franco-Jarava, Clara, Dieli-Crimi, Romina, Vila-Pijoan, Gemma, Colobran, Roger, Pujol-Borrell, Ricardo, Hernández-González, Manuel

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Th1-skewed profile and excessive production of proinflammatory cytokines in a NFKB1-deficient patient with CVID and severe gastrointestinal manifestations von Dieli-Crimi, Romina, Martínez-Gallo, Mónica, Franco-Jarava, Clara, Antolin, Maria, Blasco, Laura, Paramonov, Ida, Semidey, Maria E., Álvarez Fernández, Antoni, Molero, Xavier, Velásquez, Julio, Martín-Nalda, Andrea, Pujol-Borrell, Ricardo, Colobran, Roger

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Systematic Review and Meta-analysis Show 3% of Patients With Celiac Disease in Spain to be Negative for HLA-DQ2.5 and HLA-DQ8 von Fernández-Bañares, Fernando, Arau, Beatriz, Dieli-Crimi, Romina, Rosinach, Mercè, Nuñez, Concepción, Esteve, Maria

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Activation-induced deaminase is critical for the establishment of DNA methylation patterns prior to the germinal center reaction von Català-Moll, Francesc, Ferreté-Bonastre, Anna G, Li, Tianlu, Weichenhan, Dieter, Lutsik, Pavlo, Ciudad, Laura, Álvarez-Prado, Ángel F, Rodríguez-Ubreva, Javier, Klemann, Christian, Speckmann, Carsten, Vilas-Zornoza, Amaya, Abolhassani, Hassan, Martínez-Gallo, Mónica, Dieli-Crimi, Romina, Rivière, Jacques G, Martín-Nalda, Andrea, Colobran, Roger, Soler-Palacín, Pere, Kracker, Sven, Hammarström, Lennart, Prosper, Felipe, Durandy, Anne, Grimbacher, Bodo, Plass, Christoph, Ballestar, Esteban

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Evaluation of T cells in blood after a short gluten challenge for coeliac disease diagnosis von López-Palacios, Natalia, Pascual, Virginia, Castaño, Mercedes, Bodas, Andrés, Fernández-Prieto, Marta, Espino-Paisán, Laura, Martínez-Ojinaga, Eva, Salazar, Isabel, Martínez-Curiel, Raquel, Rey, Enrique, Estrada, Lourdes, Molero-Abraham, Magdalena, Reche, Pedro A., Dieli-Crimi, Romina, Núñez, Concepción

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An autoimmune polyglandular syndrome complicated with celiac disease and autoimmune hepatitis von Dieli-Crimi, Romina, Núñez, Concepción, Estrada, Lourdes, López-Palacios, Natalia

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Development of an Expert-Based Scoring System for Early Identification of Patients with Inborn Errors of Immunity in Primary Care Settings – the PIDCAP Project von Rivière, Jacques G, Carot-sans, Gerard, Piera-jiménez, Jordi, De La Torre, Sergi, Pidcap Expert Group, Alsina, Laia, Bielsa Masdeu, Ana Mª, Bosom Diumenjó, Maria, Carbone, Javier, Carreras, Carmen, Deya-martínez, Angela, Dieli-crimi, Romina, Espiau, María, Fernández Pereira, Luis, González, I, Juan, Manel, Llobet, Pilar, Martín-nalda, Andrea, Mendez, Maria, Neth, Olaf, Ocejo-vinyals, J. Gonzalo, Olbrich, Peter, Rodríguez, J. C, Rodríguez-vigil Iturrate, Carmen, Rodrigo, Carlos, Santos Pérez, Juan Luis, Cos, Xavier, Serra-picamal, Xavier, Soler-palacin, Pere

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Common Variable Immunodeficiency and Neurodevelopmental Delay Due to a 13Mb Deletion on Chromosome 4 Including the NFKB1 Gene : A Case Report von Franco-Jarava, Clara, Valenzuela, Irene, Riviere, Jacques G, Garcia-Prat, Marina, Martínez Gallo, Mónica, Dieli-Crimi, Romina, Castells Sarret, Neus, Batlle-Masó, Laura, Soler-Palacín, Pere, Colobrán Oriol, Roger, Universitat Autònoma de Barcelona

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