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

Innate Lymphoid Cell Phenotypic and Functional Alterations in Patients With Systemic Juvenile Idiopathic Arthritis

系统性幼年特发性关节炎患者的先天性淋巴细胞表型和功能改变

Quatrini, Linda; Ciancaglini, Cecilia; Caiello, Ivan; Santopolo, Silvia; Pardeo, Manuela; Matteo, Valentina; Loricchio, Elena; Amodio, Donato; Morrocchi, Elena; Olivieri, Giulio; Palma, Paolo; Insalaco, Antonella; Natale, Marco Francesco; De Matteis, Arianna; Tumino, Nicola; Bracaglia, Claudia; Vacca, Paola; Moretta, Lorenzo; De Benedetti, Fabrizio; Prencipe, Giusi

Correction to: Anifrolumab in Monogenic Lupus caused by TREX1 Mutation

更正:阿尼弗鲁单抗治疗由TREX1突变引起的单基因狼疮

Moran-Alvarez, Patricia; Messia, Virginia; Matteo, Valentina; Soscia, Francesca; Prencipe, Giusi; Benedetti, Fabrizio De; Insalaco, Antonella

Nlrp2 deletion ameliorates kidney damage in a mouse model of cystinosis

Nlrp2 缺失可减轻胱氨酸病小鼠模型中的肾脏损伤

Rossi, Marianna Nicoletta; Matteo, Valentina; Diomedi-Camassei, Francesca; De Leo, Ester; Devuyst, Olivier; Lamkanfi, Mohamed; Caiello, Ivan; Loricchio, Elena; Bellomo, Francesco; Taranta, Anna; Emma, Francesco; De Benedetti, Fabrizio; Prencipe, Giusi

Common bone marrow signature in COVID-19-associated multisystem inflammatory syndrome in children: A first-wave small case series experience

儿童 COVID-19 相关多系统炎症综合征的常见骨髓特征:第一波小病例系列经验

De Ioris, Maria Antonietta; Scarselli, Alessia; Bracaglia, Claudia; Perrotta, Daniela; Bernardi, Stefania; Santilli, Veronica; Ceglie, Giulia; Fabozzi, Francesco; Agrati, Chiara; Prencipe, Giusi; Alaggio, Rita; Mastronuzzi, Angela; De Vito, Rita

Monocytes From Patients With Macrophage Activation Syndrome and Secondary Hemophagocytic Lymphohistiocytosis Are Hyperresponsive to Interferon Gamma.

巨噬细胞活化综合征和继发性噬血细胞性淋巴组织细胞增生症患者的单核细胞对γ干扰素反应过度

Pascarella Antonia, Bracaglia Claudia, Caiello Ivan, Arduini Alessia, Moneta Gian Marco, Rossi Marianna Nicoletta, Matteo Valentina, Pardeo Manuela, De Benedetti Fabrizio, Prencipe Giusi

Blood-based test for diagnosis and functional subtyping of familial Mediterranean fever

用于诊断和功能分型家族性地中海热的血液检测

Van Gorp, Hanne; Huang, Linyan; Saavedra, Pedro; Vuylsteke, Marnik; Asaoka, Tomoko; Prencipe, Giusi; Insalaco, Antonella; Ogunjimi, Benson; Jeyaratnam, Jerold; Cataldo, Ilaria; Jacques, Peggy; Vermaelen, Karim; Dullaers, Melissa; Joos, Rik; Sabato, Vito; Stella, Alessandro; Frenkel, Joost; De Benedetti, Fabrizio; Dehoorne, Joke; Haerynck, Filomeen; Calamita, Giuseppe; Portincasa, Piero; Lamkanfi, Mohamed

Chitotriosidase as a Novel Biomarker for Therapeutic Monitoring of Nephropathic Cystinosis

几丁质酶作为肾病性胱氨酸病治疗监测的新型生物标志物

Veys, Koenraad R P; Elmonem, Mohamed A; Van Dyck, Maria; Janssen, Mirian C; Cornelissen, Elisabeth A M; Hohenfellner, Katharina; Prencipe, Giusi; van den Heuvel, Lambertus P; Levtchenko, Elena

Mannose Binding Lectin, S100 B Protein, and Brain Injuries in Neonates With Perinatal Asphyxia

甘露糖结合凝集素、S100 B 蛋白和围产期窒息新生儿脑损伤

Auriti, Cinzia; Prencipe, Giusi; Inglese, Rita; Moriondo, Maria; Nieddu, Francesco; Mondì, Vito; Longo, Daniela; Bucci, Silvia; Del Pinto, Tamara; Timelli, Laura; Di Ciommo, Vincenzo Maria

Is fibrodysplasia ossificans progressiva an interleukin-1 driven auto-inflammatory syndrome?

进行性骨化性纤维发育不良是一种由白细胞介素-1驱动的自身炎症综合征吗?

Haviv, Ruby; Moshe, Veronica; De Benedetti, Fabrizio; Prencipe, Giusi; Rabinowicz, Noa; Uziel, Yosef

An unusual presentation of purine nucleoside phosphorylase deficiency mimicking systemic juvenile idiopathic arthritis complicated by macrophage activation syndrome.

嘌呤核苷磷酸化酶缺乏症的一种不寻常表现,类似于全身性幼年特发性关节炎,并伴有巨噬细胞活化综合征

Arduini Alessia, Marasco Emiliano, Marucci Giulia, Pardeo Manuela, Insalaco Antonella, Caiello Ivan, Moneta Gian Marco, Prencipe Giusi, De Benedetti Fabrizio, Bracaglia Claudia