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

A Complex Neurodevelopmental Phenotype Resembling a Chromatinopathy With Concurrent 7p Duplication and 10p Deletion Involving ZMYND11 : A Case Report and Literature Review

一种复杂的神经发育表型,类似于染色质病变,伴有7p重复和10p缺失,涉及ZMYND11基因:病例报告及文献综述

Tolosana, Jose M; Berne, Paola; Mont, Lluis; Heras, Magda; Berruezo, Antonio; Monteagudo, Joan; Tamborero, David; Benito, Begoña; Brugada, Josep; Minale, Elia Marco Paolo; Martone, Stefania; Criscuolo, Chiara; Marra, Roberta; Lasorsa, Vito Alessandro; Ruggiero, Raffaella; Suero, Teresa; Capasso, Mario; Andolfo, Immacolata; Iolascon, Achille; Russo, Roberta; Pinelli, Michele

Additive effect of multiple genetic variants in SEC23B and PIEZO1 on iron metabolism dyshomeostasis in hereditary anemias

SEC23B 和 PIEZO1 中多个遗传变异对遗传性贫血中铁代谢失衡的累加效应

Nostroso, Antonella; Marra, Roberta; Rosato, Barbara Eleni; Iscaro, Anthony; Esposito, Federica Maria; D'Onofrio, Vanessa; Dionisi, Manuela; Ribersani, Michela; Giordano, Francesca; Bulla, Anna; Del Vecchio, Giovanni Carlo; Scianguetta, Saverio; Mandrile, Giorgia; Ceglie, Teresa; Scudiero, Olga; Ferrero, Giovanni Battista; Perrotta, Silverio; Iolascon, Achille; Andolfo, Immacolata; Russo, Roberta

Targeted Therapy for a Rare PDGFRB-Rearranged Myeloproliferative Neoplasm: A Case Report

针对罕见PDGFRB重排骨髓增生性肿瘤的靶向治疗:病例报告

Barbato, Cosimo; Lasorsa, Vito A; Grimaldi, Francesco; Errichiello, Santa; Pisano, Ida; Capuozzo, Maurizio; Capone, Mariangela; Izzo, Viviana; Quarantelli, Fabrizio; Potenza, Alessandra; Visconti, Roberta; Galdiero, Alessandra; Zanniti, Angelo; Prete, Ciro Del; Femiano, Teresa; Esposito, Giuseppina; Pugliese, Novella; Russo, Roberta; Capasso, Mario; Izzo, Barbara

HIF-1α as a Central Regulator of Monocyte Responses to Hypoxia

HIF-1α作为单核细胞对缺氧反应的核心调节因子

Lampiasi, Nadia; Russo, Roberta

A Complex Neurodevelopmental Phenotype Resembling a Chromatinopathy With Concurrent 7p Duplication and 10p Deletion Involving ZMYND11: A Case Report and Literature Review

一种复杂的神经发育表型,类似于染色质病变,伴有7p重复和10p缺失,涉及ZMYND11基因:病例报告及文献综述

Minale, Elia Marco Paolo; Martone, Stefania; Criscuolo, Chiara; Marra, Roberta; Lasorsa, Vito Alessandro; Ruggiero, Raffaella; Suero, Teresa; Capasso, Mario; Andolfo, Immacolata; Iolascon, Achille; Russo, Roberta; Pinelli, Michele

Mitapivat metabolically reprograms human β-thalassemic erythroblasts, increasing their responsiveness to oxidation

Mitapivat 可代谢性地重编程人类β-地中海贫血红细胞,增强其对氧化反应的敏感性。

Siciliano, Angela; D'Alessandro, Angelo; Matte, Alessandro; Bisello, Giovanni; Bertoldi, Mariarita; Dzieciatkowska, Monika; Argabright, Amy; Pozzetto, Richard Huot; Riccardi, Veronica; Mattarei, Andrea; Ongaro, Alberto; Ceolan, Jacopo; Russo, Roberta; Rivadeneyra, Leonardo; Wind-Rotolo, Megan; Iolascon, Achille; Brugnara, Carlo; De Franceschi, Lucia

Temocillin: A Narrative Review of Its Clinical Reappraisal

替莫西林:临床重新评价的叙述性综述

Cosimi, Lavinia; Zerbato, Verena; Grasselli Kmet, Nina; Oliva, Alessandra; Cogliati Dezza, Francesco; Geremia, Nicholas; Cattaneo, Dario; Nadrah, Kristina; Pirs, Mateja; Saletinger, Rajko; Nunnari, Alessio; Mearelli, Filippo; Di Girolamo, Filippo Giorgio; Avena, Graziana; Russo, Roberta; Fabiani, Carolina; Venturini, Sergio; Principe, Luigi; Nicolò, Giovanna Maria; Di Bella, Stefano

COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNet

欧洲注册登记处ERN-EuroBloodNet的研究结果显示,患有红细胞疾病的患者感染COVID-19的情况较为严重。

Velasco Puyo, Pablo; Christou, Soteroula; Campisi, Saveria; Rodríguez-Sánchez, Maria A; Reidel, Sara; Perez-Hoyo, Santiago; Mota, Miriam; Savvidou, Irene; Rekleiti, Anna; Salvo, Alessandra; Voi, Vincenzo; Ferrero, Giovanni Battista; Mandrile, Giorgia; Gaglioti, Carmen Maria; Cela, Elena; Ponce-Salas, Beatriz; Bardón-Cancho, Eduardo J; Flevari, Pagona; Voskaridou-Dimoula, Ersi; Nur, Erfan; Biemond, Bart J; Delaporta, Polynexi; Beneitez-Pastor, David; Collado Gimbert, Anna; Spasiano, Anna; Besse-Hammer, Tatiana; Lafiatis, Ioannis G; Dedeken, Laurence; Raso, Simona; Ruiz-Llobet, Anna; Bagnato, Sabrina; Labarque, Veerle; Glenthøj, Andreas; Ruffo, Giovan Battista; Guerzoni, Maria Elena; Hafraoui, Kaoutar; Pistoia, Laura; Rosso, Rosamaria; Tagliaferri, Laura; Gonzalez-Urdiales, Paula; Benghiat, Fleur Samantha; de Montalembert, Mariane; Teles, Maria Jose; Vanderfaeillie, Anna; Bertoni, Elisa; Cuzzubbo, Daniela; Ferreira, Teresa; Saunders, Christopher J; Stiakaki, Eftichia; Van de Velde, Ann L; Diamantidis, Michael D; Kerkhoffs, Jean-Louis H; Oliveira, Marisa I; Quota, Alessandra; Russo, Roberta; Van Damme, An; Argüello Marina, María; Lorite Reggiori, Mikael; Rijneveld, Anita W; Rodríguez Gallego, Alexis; Colombatti, Raffaella; Iolascon, Achille; Taher, Ali; Gulbis, Béatrice; Roy, Noémi B A; Mañú-Pereira, María Del Mar

Molecular analysis of T-cell Acute Lymphoblastic Leukemia arising after Essential Thrombocythemia foreshadows a distinct clonal route for lymphoid blast crisis in Philadelphia-negative chronic myeloproliferative neoplasm: a case report with literary review

原发性血小板增多症后发生的T细胞急性淋巴细胞白血病的分子分析预示着费城染色体阴性慢性骨髓增殖性肿瘤淋巴母细胞危象的独特克隆途径:病例报告及文献综述

Grimaldi, Francesco; Memoli, Mara; Avilia, Simona; Russo, Roberta; Scalia, Giulia; Visconti, Roberta; Errichiello, Santa; Izzo, Barbara; Pane, Fabrizio

Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemia

关于缺铁和缺铁性贫血的诊断、治疗和预防的建议

Iolascon, Achille; Andolfo, Immacolata; Russo, Roberta; Sanchez, Mayka; Busti, Fabiana; Swinkels, Dorine; Aguilar Martinez, Patricia; Bou-Fakhredin, Rayan; Muckenthaler, Martina U; Unal, Sule; Porto, Graça; Ganz, Tomas; Kattamis, Antonis; De Franceschi, Lucia; Cappellini, Maria Domenica; Munro, Malcolm G; Taher, Ali