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Andersson, Nadine G; Labarque, Veerle; Kartal-Kaess, Mutlu; Pinto, Fernando; Mikkelsen, Torben Stamm; Ljung, Rolf; Group, PedNet Study (2024). Factor VIII genotype and the risk of developing high-responding or low-responding inhibitors in severe hemophilia A: data from the PedNet Hemophilia Cohort of 1,202 children. Haematologica, 109(4), pp. 1293-1296. Ferrata-Storti Foundation 10.3324/haematol.2023.284095
Labarque, Veerle; Mancuso, Maria Elisa; Kartal-Kaess, Mutlu; Ljung, Rolf; Mikkelsen, Torben S; Andersson, Nadine G (2023). F8/F9 variants in the population-based PedNet Registry cohort compared with locus-specific genetic databases of the European Association for Haemophilia and Allied Disorders and the Centers for Disease Control and Prevention Hemophilia A or Hemophilia B Mutation Project. Research and practice in thrombosis and haemostasis, 7(1), p. 100036. Wiley 10.1016/j.rpth.2023.100036
Connor, Philip; Sánchez van Kammen, Mayte; Lensing, Anthonie W A; Chalmers, Elizabeth; Kállay, Krisztián; Hege, Kerry; Simioni, Paolo; Biss, Tina; Bajolle, Fanny; Bonnet, Damien; Grunt, Sebastian; Kumar, Riten; Lvova, Olga; Bhat, Rukhmi; Van Damme, An; Palumbo, Joseph; Santamaria, Amparo; Saracco, Paola; Payne, Jeanette; Baird, Susan; ... (2020). Safety and efficacy of rivaroxaban in pediatric cerebral venous thrombosis (EINSTEIN-Jr CVT). Blood advances, 4(24), pp. 6250-6258. American Society of Hematology 10.1182/bloodadvances.2020003244
Andersson, Nadine G; Labarque, Veerle; Letelier, Anna; Mancuso, Maria Elisa; Bührlen, Martina; Fischer, Kathelijn; Kartal-Kaess, Mutlu; Koskenvuo, Minna; Mikkelsen, Torben; Ljung, Rolf (2020). Novel F8 and F9 gene variants from the PedNet hemophilia registry classified according to ACMG/AMP guidelines. Human mutation, 41(12), pp. 2058-2072. Wiley 10.1002/humu.24117
