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

Dominant negative variants in ITPR3 impair T cell Ca2+ dynamics causing combined immunodeficiency.

ITPR3 中的显性负性变异会损害 T 细胞 Ca2+ 动力学,导致联合免疫缺陷

Blanco Elena, Camps Carme, Bahal Sameer, Kerai Mohit D, Ferla Matteo P, Rochussen Adam M, Handel Adam E, Golwala Zainab M, Spiridou Goncalves Helena, Kricke Susanne, Klein Fabian, Zhang Fang, Zinghirino Federica, Evans Grace, Keane Thomas M, Lizot Sabrina, Kusters Maaike A A, Iro Mildred A, Patel Sanjay V, Morris Emma C, Burns Siobhan O, Radcliffe Ruth, Vasudevan Pradeep, Price Arthur, Gillham Olivia, Valdebenito Gabriel E, Stewart Grant S, Worth Austen, Adams Stuart P, Duchen Michael, André Isabelle, Adams David J, Santili Giorgia, Gilmour Kimberly C, Holländer Georg A, Davies E Graham, Taylor Jenny C, Griffiths Gillian M, Thrasher Adrian J, Dhalla Fatima, Kreins Alexandra Y

Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UK

英国原发性和继发性免疫缺陷患者感染SARS-CoV-2后的预后

Shields, Adrian M; Anantharachagan, Ariharan; Arumugakani, Gururaj; Baker, Kenneth; Bahal, Sameer; Baxendale, Helen; Bermingham, William; Bhole, Malini; Boules, Evon; Bright, Philip; Chopra, Charu; Cliffe, Lucy; Cleave, Betsy; Dempster, John; Devlin, Lisa; Dhalla, Fatima; Diwakar, Lavanya; Drewe, Elizabeth; Duncan, Christopher; Dziadzio, Magdalena; Elcombe, Suzanne; Elkhalifa, Shuayb; Gennery, Andrew; Ghanta, Harichandrana; Goddard, Sarah; Grigoriadou, Sofia; Hackett, Scott; Hayman, Grant; Herriot, Richard; Herwadkar, Archana; Huissoon, Aarnoud; Jain, Rashmi; Jolles, Stephen; Johnston, Sarah; Khan, Sujoy; Laffan, James; Lane, Peter; Leeman, Lucy; Lowe, David M; Mahabir, Shanti; Lochlainn, Dylan James Mac; McDermott, Elizabeth; Misbah, Siraj; Moghaddas, Fiona; Morsi, Hadeil; Murng, Sai; Noorani, Sadia; O'Brien, Rachael; Patel, Smita; Price, Arthur; Rahman, Tasneem; Seneviratne, Suranjith; Shrimpton, Anna; Stroud, Catherine; Thomas, Moira; Townsend, Katie; Vaitla, Prashantha; Verma, Nisha; Williams, Anthony; Burns, Siobhan O; Savic, Sinisa; Richter, Alex G

Inborn errors of thymic stromal cell development and function

胸腺基质细胞发育和功能的先天性缺陷

Kreins, Alexandra Y; Maio, Stefano; Dhalla, Fatima

Histology of Interstitial Lung Disease in Common Variable Immune Deficiency

常见变异型免疫缺陷病间质性肺病的组织学

Dhalla, Fatima; Lochlainn, Dylan J Mac; Chapel, Helen; Patel, Smita Y

Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation

176例接受或未接受造血干细胞移植治疗的X连锁高IgM综合征患者的长期疗效

de la Morena, M Teresa; Leonard, David; Torgerson, Troy R; Cabral-Marques, Otavio; Slatter, Mary; Aghamohammadi, Asghar; Chandra, Sharat; Murguia-Favela, Luis; Bonilla, Francisco A; Kanariou, Maria; Damrongwatanasuk, Rongras; Kuo, Caroline Y; Dvorak, Christopher C; Meyts, Isabelle; Chen, Karin; Kobrynski, Lisa; Kapoor, Neena; Richter, Darko; DiGiovanni, Daniela; Dhalla, Fatima; Farmaki, Evangelia; Speckmann, Carsten; Español, Teresa; Shcherbina, Anna; Hanson, Imelda Celine; Litzman, Jiri; Routes, John M; Wong, Melanie; Fuleihan, Ramsay; Seneviratne, Suranjith L; Small, Trudy N; Janda, Ales; Bezrodnik, Liliana; Seger, Reinhard; Raccio, Andrea Gomez; Edgar, J David M; Chou, Janet; Abbott, Jordan K; van Montfrans, Joris; González-Granado, Luis Ignacio; Bunin, Nancy; Kutukculer, Necil; Gray, Paul; Seminario, Gisela; Pasic, Srdjan; Aquino, Victor; Wysocki, Christian; Abolhassani, Hassan; Dorsey, Morna; Cunningham-Rundles, Charlotte; Knutsen, Alan P; Sleasman, John; Costa Carvalho, Beatriz Tavares; Condino-Neto, Antonio; Grunebaum, Eyal; Chapel, Helen; Ochs, Hans D; Filipovich, Alexandra; Cowan, Mort; Gennery, Andrew; Cant, Andrew; Notarangelo, Luigi D; Roifman, Chaim M

FOXN1 deficient nude severe combined immunodeficiency

FOXN1缺陷型裸重症联合免疫缺陷

Rota, Ioanna A; Dhalla, Fatima

Challenges in the Role of Gammaglobulin Replacement Therapy and Vaccination Strategies for Hematological Malignancy

血液系统恶性肿瘤中丙种球蛋白替代疗法和疫苗接种策略面临的挑战

Sánchez-Ramón, Silvia; Dhalla, Fatima; Chapel, Helen

Identification of a novel mutation in MAGT1 and progressive multifocal leucoencephalopathy in a 58-year-old man with XMEN disease

在一名患有XMEN病的58岁男性患者中,鉴定出MAGT1基因的新突变和进行性多灶性白质脑病。

Dhalla, Fatima; Murray, Sarah; Sadler, Ross; Chaigne-Delalande, Benjamin; Sadaoka, Tomohiko; Soilleux, Elizabeth; Uzel, Gulbu; Miller, Joanne; Collins, Graham Peter; Hatton, Christian Simon Ross; Bhole, Malini; Ferry, Berne; Chapel, Helen M; Cohen, Jeffrey I; Patel, Smita Y