日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Prognostic Factors of Late-onset Hearing Loss in Infants With Congenital Cytomegalovirus and Normal Audiologic Assessment at Birth

先天性巨细胞病毒感染且出生时听力评估正常的婴儿迟发性听力损失的预后因素

Buonsenso, Danilo; Pedrero-Tomé, Roberto; Raimondi, Francesco; Salomé, Serena; Papaevangelou, Vassiliki; Syridou, Garyfallia; Ríos-Barnés, María; Fortuny, Clàudia; Villaverde, Serena; de Vergas, Joaquín; Baquero-Artigao, Fernando; Rodríguez-Molino, Paula; Frick, Marie Antoinette; Álvarez-Vallejo, Beatriz; Saavedra-Lozano, Jesús; Fougere, Yves; Del Valle, Rut; Ara-Montojo, Fátima; Foulon, Ina; Mignogna, Simona; Muga Zuriarrain, Oihana; Lyall, Hermione; Vives-Oñós, Isabel; Colino, Elena; Tsiatsiou, Olga; Moliner, Elisenda; Garofoli, Francesca; Cuadrado, Irene; Blázquez-Gamero, Daniel

Torque teno virus: a potential marker of immune reconstitution in youths with vertically acquired HIV

扭矩病毒:垂直感染HIV的青少年免疫重建的潜在标志物

Tarancon-Diez, Laura; Carrasco, Itziar; Montes, Laura; Falces-Romero, Iker; Vazquez-Alejo, Elena; Jiménez de Ory, Santiago; Dapena, Marta; Iribarren, Jose Antonio; Díez, Cristina; Ramos-Ruperto, Luis; Colino, Elena; Calvo, Cristina; Muñoz-Fernandez, Mª Ángeles; Navarro, María Luisa; Sainz, Talía

Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

患有遗传性 MyD88 和 IRAK-4 缺陷的人类易患低氧性 COVID-19 肺炎

García-García, Ana; Pérez de Diego, Rebeca; Flores, Carlos; Rinchai, Darawan; Solé-Violán, Jordi; Deyà-Martínez, Àngela; García-Solis, Blanca; Lorenzo-Salazar, José M; Hernández-Brito, Elisa; Lanz, Anna-Lisa; Moens, Leen; Bucciol, Giorgia; Almuqamam, Mohamed; Domachowske, Joseph B; Colino, Elena; Santos-Perez, Juan Luis; Marco, Francisco M; Pignata, Claudio; Bousfiha, Aziz; Turvey, Stuart E; Bauer, Stefanie; Haerynck, Filomeen; Ocejo-Vinyals, Javier Gonzalo; Lendinez, Francisco; Prader, Seraina; Naumann-Bartsch, Nora; Pachlopnik Schmid, Jana; Biggs, Catherine M; Hildebrand, Kyla; Dreesman, Alexandra; Cárdenes, Miguel Ángel; Ailal, Fatima; Benhsaien, Ibtihal; Giardino, Giuliana; Molina-Fuentes, Agueda; Fortuny, Claudia; Madhavarapu, Swetha; Conway, Daniel H; Prando, Carolina; Schidlowski, Laire; Martínez de Saavedra Álvarez, María Teresa; Alfaro, Rafael; Rodríguez de Castro, Felipe; Meyts, Isabelle; Hauck, Fabian; Puel, Anne; Bastard, Paul; Boisson, Bertrand; Jouanguy, Emmanuelle; Abel, Laurent; Cobat, Aurélie; Zhang, Qian; Casanova, Jean-Laurent; Alsina, Laia; Rodríguez-Gallego, Carlos

Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds.

部分隐性 IFN-γR1 缺乏症:来自 11 个家族的 14 名患者的遗传、免疫学和临床特征

Sologuren Ithaisa, Boisson-Dupuis Stéphanie, Pestano Jose, Vincent Quentin Benoit, Fernández-Pérez Leandro, Chapgier Ariane, Cárdenes María, Feinberg Jacqueline, García-Laorden M Isabel, Picard Capucine, Santiago Esther, Kong Xiaofei, Jannière Lucile, Colino Elena, Herrera-Ramos Estefanía, Francés Adela, Navarrete Carmen, Blanche Stéphane, Faria Emilia, Remiszewski Pawel, Cordeiro Ana, Freeman Alexandra, Holland Steven, Abarca Katia, Valerón-Lemaur Mónica, Gonçalo-Marques José, Silveira Luisa, García-Castellano José Manuel, Caminero José, Pérez-Arellano José Luis, Bustamante Jacinta, Abel Laurent, Casanova Jean-Laurent, Rodríguez-Gallego Carlos