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

Indications for haematopoietic cell transplantation and CAR-T for haematological diseases, solid tumours and immune disorders: 2025 EBMT practice recommendations

造血干细胞移植和CAR-T疗法在血液系统疾病、实体瘤和免疫系统疾病中的适应症:2025年欧洲骨髓移植协会(EBMT)实践指南

Greco, R; Ruggeri, A; McLornan, D P; Snowden, J A; Alexander, T; Angelucci, E; Averbuch, D; Bazarbachi, A; Hazenberg, M D; Kalwak, K; Kenyon, M; Mekelenkamp, H; Neven, B; Pedrazzoli, P; Peric, Z; Risitano, A M; Sánchez-Ortega, I; Ciceri, F; Sureda, A

Hypomorphic RAG deficiency: impact of disease burden on survival and thymic recovery argues for early diagnosis and HSCT

RAG 功能减退缺陷:疾病负担对生存和胸腺恢复的影响提示早期诊断和造血干细胞移植的必要性。

Schuetz, C; Gerke, J; Ege, M; Walter, J; Kusters, M; Worth, A; Kanakry, J A; Dimitrova, D; Wolska-Kuśnierz, B; Chen, K; Unal, E; Karakukcu, M; Pashchenko, O; Leiding, J; Kawai, T; Amrolia, P J; Berghuis, D; Buechner, J; Buchbinder, D; Cowan, M J; Gennery, A R; Güngör, T; Heimall, J; Miano, M; Meyts, I; Morris, E C; Rivière, J; Sharapova, S O; Shaw, P J; Slatter, M; Honig, M; Veys, P; Fischer, A; Cavazzana, M; Moshous, D; Schulz, A; Albert, M H; Puck, J M; Lankester, A C; Notarangelo, L D; Neven, B

The first steps towards a diverse and inclusive EBMT: a position paper

迈向多元化和包容性EBMT的第一步:一份立场文件

Montoto, S; Snowden, J A; Chabannon, C; Corbacioglu, S; de la Camara, R; Dolstra, H; Greco, R; Gusi, A; Hamad, N; Kenyon, M; Kröger, N; Mohty, M; Murray, J; Mueller, A; Neven, B; Peffault de Latour, R; Peric, Z; Sánchez-Ortega, I; Sureda, A; Verhoeven, B; Villar, A; Yakoub-Agha, I

EBMT/ESID inborn errors working party guidelines for hematopoietic stem cell transplantation for inborn errors of immunity

欧洲骨髓移植协会/欧洲传染病学会先天性免疫缺陷工作组关于造血干细胞移植治疗先天性免疫缺陷的指南

Lankester, A C; Albert, M H; Booth, C; Gennery, A R; Güngör, T; Hönig, M; Morris, E C; Moshous, D; Neven, B; Schulz, A; Slatter, M; Veys, P

Clinical Heterogeneity of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome: A French Multicenter Retrospective Study

免疫失调、多内分泌病、肠病、X连锁综合征的临床异质性:一项法国多中心回顾性研究

Duclaux-Loras, R; Charbit-Henrion, F; Neven, B; Nowak, J; Collardeau-Frachon, S; Malcus, C; Ray, P F; Moshous, D; Beltrand, J; Goulet, O; Cerf-Bensussan, N; Lachaux, A; Rieux-Laucat, F; Ruemmele, F M

PW02-022 - Recurrent fever syndromes: multiple gene mutations

PW02-022 - 复发性发热综合征:多基因突变

Sanner, Helga; Schwartz, Thomas; Flatø, Berit; Vistnes, Maria; Christensen, Geir; Sjaastad, Ivar; Piram, M; Koné-Paut, I; Gattorno, M; Ruperto, N; Kawai, T; Nishikomori, R; Awaya, M; Nakagawa, K; Izawa, K; Yasumi, T; Ohara, O; Heike, T; Alberighi, O Della Casa; Accame, L; Frenkel, J; Gattorno, M; Martini, A; Neven, B; Quartier, P; Pierotti, F; Turchetti, G; Caorsi, R; Insalaco, A; Marotto, D; Frenkel, J; Martini, A; De Benedetti, F; Gattorno, M; Bohm, M; Dolezalova, P; Lachmann, H; Modesto, C; Touitou, I; Woo, P; Finetti, M; Hentgen, V; Cantarini, L; De Benedetti, F; Gallizzi, R; Obici, L; Manna, R; Gallo, E; Ruperto, N; Gattorno, M

Morphometry and epidermal fas expression of unexposed aged versus young skin

未暴露于外界环境的老年皮肤与年轻皮肤的形态测量和表皮Fas表达

El-Aal, Nagwa H Abd; El-Wadood, Faten A Abd; Moftah, Nayera H; El-Hakeem, Mohamed S; El-Shaal, Abdalla Y; Hassan, Neven B

Therapeutic approaches for the treatment of new onset and flared juvenile systemic lupus erythematosus with active renal disease: an international multicenter PRINTO study

针对伴有活动性肾脏疾病的新发和复发性幼年系统性红斑狼疮的治疗方法:一项国际多中心PRINTO研究

Ruperto, Nicolino; Martini, Alberto; Toplak, N; Frenkel, J; Ozen, S; De Benedetti, F; Hofer, M; Kone-Paut, I; Girschick, H; Neven, B; Ozdogan, H; Kummerle-Deschner, J; Arostegui, J; Simon, A; Stojanov, S; Vesely, R; Wouters, C; Hentgen, V; Rose, C; Dolezalova, P; Lachmann, H; Woo, P; Touitou, I; Martini, A; Ruperto, N; Gattorno, M; Miettunen, P; Pistorio, A; Ravelli, A; Oliveira, S; Alessio, M; Cuttica, R; Mihaylova, D; Espada, G; Pasic, S; Cortis, E; Ozen, S; Porras, O; Sztajnbok, F; Palmisani, E; Martini, A; Ruperto, N

Mevalonate kinase deficiency (MKD): long-term follow-up of clinical and biological features in 40 patients

甲羟戊酸激酶缺乏症(MKD):40例患者的临床和生物学特征长期随访

Kim, Jin-Min; Song, Beom-Seok; Hong, Sung-Gil; Sohn, Hee-Jung; Baik, Hyunwook; Sung, Mi-Kyung; Florkin, B; Cuisset, L; Acquaviva-Bourdain, C; Rabier, D; Neven, B; Quartier, P; Prieur, AM