Efficacy and safety of fitusiran prophylaxis in people with haemophilia A or haemophilia B with inhibitors (ATLAS-INH): a multicentre, open-label, randomised phase 3 trial by Young, Guy, Srivastava, Alok, Kavakli, Kaan, Ross, Cecil, Sathar, Jameela, You, Chur-Woo, Tran, Huyen, Sun, Jing, Wu, Runhui, Poloskey, Stacey, Qiu, Zhiying, Kichou, Salim, Andersson, Shauna, Mei, Baisong, Rangarajan, Savita

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Real‐world analysis of patients with haemophilia A and haemophilia A carriers in the United States: Demographics, clinical characteristics and costs by Batt, Katharine, Xing, Shan, Kuharic, Maja, Bullano, Michael, Caicedo, Jorge, Chakladar, Sreya, Markan, Riddhi, Farahbakhshian, Sepehr

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The safety of plasma‐derived haemophilia factor concentrates – comments on “Deep viral metagenomics in patients with haemophilia receiving plasma‐derived coagulation factor concentrates” Nunes Valença I et al. (2021). Deep viral metagenomics in patients with haemophilia receiving plasma‐derived coagulation factor concentrates. Haemophilia. https://doi.org/10.1111/hae.14382 by Farrugia, Albert

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Current and future therapies for haemophilia—Beyond factor replacement therapies by Nogami, Keiji, Shima, Midori

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Gene therapy for haemophilia by Sharma, Akshay, Easow Mathew, Manu, Sriganesh, Vasumathi, Reiss, Ulrike M

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Haemophilia early arthropathy detection with ultrasound and haemophilia joint health score in the moderate haemophilia (MoHem) study by Måseide, Ragnhild J., Berntorp, Erik, Astermark, Jan, Hansen, Jessica, Olsson, Anna, Bruzelius, Maria, Frisk, Tony, Aspdahl, Magnus, Nummi, Vuokko, Tjønnfjord, Geir E., Holme, Pål A.

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Activated prothrombin complex concentrate (FEIBA®) in acquired haemophilia A: a large multicentre Italian study – the FAIR Registry by Zanon, Ezio, Pasca, Samantha, Santoro, Cristina, Gamba, Gabriella, Siragusa, Sergio M., Rocino, Angiola, Cantori, Isabella, Federici, Augusto B., Mameli, Luciana, Giuffrida, Gaetano, Falanga, Anna, Lodigiani, Corrado, Santoro, Rita C., Milan, Marta, Ambaglio, Chiara, Napolitano, Mariasanta, Mazzucconi, Maria G.

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haemophilia

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How mild is mild haemophilia? by Daffunchio, Carla, Landro, Maria E., Galatro, Gustavo, Neme, Daniela, Cambiaggi, Guillermo, Moretti, Noemi, Guerrero, Virginia, Negrete, Graciela, Primiani, Laura, Caviglia, Horacio

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Identified unmet needs and proposed solutions in mild‐to‐moderate haemophilia: A summary of opinions from a roundtable of haemophilia experts by Walsh, Christopher, Boggio, Lisa, Brown‐Jones, Lanette, Miller, Rachel, Hawk, Sarah, Savage, Brittany, Hansen, Kerry, Molter, Don, Baumann, Kim, Dunn, Spencer, Skinner, Mark W., Haugstad, Kimberly, Johnson, Stormy, Davenport, Tammy, Bradbury, Margaret, Witkop, Michelle, Saad, Hossam, Cooper, David L.

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Digital haemophilia: Insights into the use of social media for haemophilia care, research and advocacy by Chen, Robert, Muralidharan, Kavitha, Samelson‐Jones, Benjamin J.

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Joint protection in haemophilia by RODRIGUEZ-MERCHAN, E. C., JIMENEZ-YUSTE, V., AZNAR, J. A., HEDNER, U., KNOBE, K., LEE, C. A., LJUNG, R., QUEROL, F., SANTAGOSTINO, E., VALENTINO, L. A., CAFFARINI, A.

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Correction to Batt K, Xing S, KuharicM, et al. Real-world analysis of patients with haemophilia A and haemophilia A carriers in the United States: Demographics, clinical characteristics and costs

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Current status of haemophilia inhibitor management in mainland China: a haemophilia treatment centres survey on treatment preferences and real‐world clinical practices by Liu, Wei, Xue, Feng, Poon, Man‐Chiu, Chen, Lingling, Jin, Zhaona, Zhang, Lei, Yang, Renchi

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Inhibitors in haemophilia A and B: Management of bleeds, inhibitor eradication and strategies for difficult‐to‐treat patients by Ljung, Rolf, Auerswald, Guenter, Benson, Gary, Dolan, Gerry, Duffy, Anne, Hermans, Cedric, Jiménez‐Yuste, Victor, Lambert, Thierry, Morfini, Massimo, Zupančić‐Šalek, Silva, Santagostino, Elena

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Guidelines for the management of acute joint bleeds and chronic synovitis in haemophilia: A United Kingdom Haemophilia Centre Doctors' Organisation (UKHCDO) guideline by Hanley, J, McKernan, A, Creagh, M D, Classey, S, McLaughlin, P, Goddard, N, Briggs, P J, Frostick, S, Giangrande, P, Wilde, J, Thachil, J, Chowdary, P

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Is haemophilia B less severe than haemophilia A? by Mannucci, P. M., Franchini, M.

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COVID‐19 and telemedicine in haemophilia in a patient with severe haemophilia A and orthopaedic surgery by Álvarez‐Román, María Teresa, De la Corte‐Rodríguez, Hortensia, Rodríguez‐Merchán, Emérito Carlos, Martín‐Salces, Mónica, Rivas‐Pollmar, María Isabel, Butta, Nora V., García‐Barcenilla, Sara, Acuña, Paula, Cebanu, Tamara, González, Elena, Monzón‐Manzano, María Elena, Jiménez‐Yuste, Víctor

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Radiosynovectomy in haemophilia by Rodriguez-Merchan, E. Carlos

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Direct data transfer of people with hereditary bleeding disorders from the Thai haemophilia treatment centre registry to the Annual Global Survey of the World Federation of Hemophilia by Chuansumrit, Ampaiwan, Youttananukorn, Worachanok, Sirachainan, Nongnuch, Natesirinilkul, Rungrote, Ruchutrakool, Theera

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