Two independent consecutive lymphoma cases carry an identical MYD88 mutation but differ in their IGVH rearrangement by Prieto‐Torres, Lucía, Trascasa, Álvaro, Manso, Rebeca, Machan, Salma, Cieza‐Diaz, Deisy, Olmedilla, Gabriel, García‐García, Mar, Ara‐Martín, Mariano, Requena, Luis, Piris, Miguel Á., Rodríguez‐Pinilla, Socorro M.

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Histiocytic hyperplasia with hemophagocytosis and acute alveolar damage in COVID-19 infection by Prieto-Pérez, Laura, Fortes, José, Soto, Carlos, Vidal-González, Ánxela, Alonso-Riaño, Marina, Lafarga, Miguel, Cortti, María José, Lazaro-Garcia, Alberto, Pérez-Tanoira, Ramón, Trascasa, Álvaro, Antonio, Anabel, Córdoba, Raúl, Rodríguez-Pinilla, Socorro María, Cedeño, Oderay, Peces-Barba, Germán, Fernández-Ormaechea, Itziar, Díez Medrano, María José, López de Las Heras, Marta, Cabello, Alfonso, Petkova, Elizabet, Álvarez, Beatriz, Carrillo, Irene, Silva, Andrés M., Castellanos, Marina, Calpena, Silvia, Valverde-Monge, Marcela, Fresneda, Diana, Rubio-Martín, Rafael, Cornejo, Ignacio, Astilleros Blanco de Cordova, Laura, de la Fuente, Soraya, Recuero, Sheila, Górgolas, Miguel, Piris, Miguel A.

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Isolated central nervous system Whipple disease by Barbero-Aznarez, Pablo, Perez-Tanoira, Ramon, Aguirre-Mollehuanca, Daniel, Trascasa-Caño, Alvaro, Fortes-Alen, Jose, Manzarbeitia-Arrambari, Felix, Castillo-Alvarez, Jorge, Montoya-Bordon, Julia, Petkova-Saiz, Elizabet, Prieto-Perez, Laura

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Deregulated cellular circuits driving immunoglobulins and complement consumption associate with the severity of COVID‐19 patients by Marcos‐Jiménez, Ana, Sánchez‐Alonso, Santiago, Alcaraz‐Serna, Ana, Esparcia, Laura, López‐Sanz, Celia, Sampedro‐Núñez, Miguel, Mateu‐Albero, Tamara, Sánchez‐Cerrillo, Ildefonso, Martínez‐Fleta, Pedro, Gabrie, Ligia, Campo Guerola, Luciana, Rodríguez‐Frade, José Miguel, Casasnovas, José M., Reyburn, Hugh T., Valés‐Gómez, Mar, López‐Trascasa, Margarita, Martín‐Gayo, Enrique, Calzada, María José, Castañeda, Santos, Fuente, Hortensia, González‐Álvaro, Isidoro, Sánchez‐Madrid, Francisco, Muñoz‐Calleja, Cecilia, Alfranca, Arantzazu

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Hereditary angioedema: The mutation spectrum of SERPING1/C1NH in a large Spanish cohort by Roche, Olga, Blanch, Alvaro, Duponchel, Christiane, Fontán, Gumersindo, Tosi, Mario, López-Trascasa, Margarita

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First case of homozygous C1 inhibitor deficiency by Blanch, Alvaro, Roche, Olga, Urrutia, Ignacio, Gamboa, Pedro, Fontán, Gumersindo, López-Trascasa, Margarita

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Evaluation of Nutritional Practices in the Critical Care patient (The ENPIC study): Does nutrition really affect ICU mortality? by Lopez-Delgado, Juan C., Bordeje-Laguna, M Luisa, Mor-Marco, Esther, Lorencio-Cardenas, Carol, Vera-Artazcoz, Paula, Iglesias-Rodriguez, Rayden, Flordelis-Lasierra, José L., Menor-Fernández, Eva M., Servia-Goixart, Lluís, Trujillano-Cabello, Javier, Escobar-Ortiz, Joan, Montserrat-Ortiz, Neus, Zapata-Rojas, Amalia, Grau-Carmona, Teodoro, Bautista-Redondo, Iris, Diaz-Castellanos, Laura, Bono, Montserrat Plaza, Montejo-Gonzalez, Juan Carlos, Temprano-Vazquez, Susana, Arjona-Diaz, Veronica, Mudarra-Reche, Carolina, Orejana-Martin, Maria, Lopez-Delgado, Juan Carlos, Lores-Obradors, Africa, Anguela-Calvet, Laura, Muñoz-Del Río, Gloria, Revelo-Esquibel, Pamela Alejandra, Luna-Solis, Stephani Maria, Salinas-Canovas, Alvaro, De Frutos-Seminario, Fernando, Rodriguez-Queralto, Oriol, Zamora-Elson, Monica, Fuente-O'Connor, Eugenia de la, Arbeloa, Carlos Seron, Bueno-Vidales, Nestor, Iglesias-Rodriguez, Rayden, Martin-Luengo, Ana, Sanchez-Miralles, Angel, Marmol-Peis, Enrique, Ruiz-Miralles, Miriam, Gonzalez-Sanz, Maria, Server-Martinez, Arantzazu, Vila-Garcia, Belen, Lorencio-Cardenas, Carol, Macaya-Redin, Laura, Aldunate-Calvo, Sara, Flordelis-Lasierra, Jose Luis, Rio, Irene Jimenez-del, Rodriguez-Roldan, Jose Manuel, Gastaldo-Simeon, Rosa, Fernandez-Ortega, Juan Francisco, Martinez-Carmona, Juan F., Lopez-Luque, Esther, Crespo-Gomez, Monica, Lopez-García, Esther, Navarro-Lacalle, Arturo, Martinez-Garcia, Pilar, Dominguez-Fernandez, Maria Inmaculada, Vera-Artazcoz, Paula, Izura-Gomez, Marta, Hernandez-Duran, Susana, Mor-Marco, Esther, Rovira-Valles, Yaiza, Philibert, Viridiana, Alcazar-Espin, Maravillas de las Nieves, Calvo-Herranz, Enrique, Manzano-Moratinos, Diego, Portugal-Rodriguez, Esther, Andaluz-Ojeda, David, Parra-Morais, Laura, Citores-Gonzalez, Rafael, Sanchez-Giron, Gloria Renedo, Navas-Moya, Elisabeth, Ferrer-Pereto, Carles, Lluch-Candal, Cristina, Leon-Cinto, Cristina, Yebenes-Reyes, Juan Carlos, Nieto-Martino, Beatriz, Vaquerizo-Alonso, Clara, Almanza-Lopez, Susana, Anton-Pascual, Jose Luis, Marin-Corral, Judith, Sistachs-Baquedano, Maite, Hacer-Puig, Maria, Picornell-Noguera, Marina, Mateu-Campos, Lidon, Martinez-Valero, Clara, Llorente-Ruiz, Beatriz, Martinez-Diaz, María Cristina, Fernandez-Salvatierra, Leticia, Millan-Taratiel, Paula, Tejada-Artigas, Antonio, Martinez-Arroyo, Ines, Araujo-Aguilar, Pilar, Fuster-Cabre, Maria, Touceda-Bravo, Alberto, Almorin-Gonzalvez, Laura, Gero-Escapa, Maria, Martinez-Barrio, Esther, Monge-Donaire, Diana

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Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations by Blanch, Alvaro, Roche, Olga, López-Granados, Eduardo, Fontán, Gumersindo, López-Trascasa, Margarita

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Erratum: Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations by Blanch, Alvaro, Roche, Olga, López-Granados, Eduardo, Fontán, Gumersindo, López-Trascasa, Margarita

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Erratum: Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations: MUTATIONS IN BRIEF by Blanch, Alvaro, Roche, Olga, López-Granados, Eduardo, Fontán, Gumersindo, López-Trascasa, Margarita

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Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations: MUTATIONS IN BRIEF by Blanch, Alvaro, Roche, Olga, López-Granados, Eduardo, Fontán, Gumersindo, López-Trascasa, Margarita

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