ID: 4120631 Artificial Intelligence Enabled Electrocardiogram Algorithm To Predict Atrial Fibrosis
Gruwez, H., Barthels, M., Haemers, P., Dhont, S., Meekers, E., Ezzat, D., Rivero-Ayerza, M., Nuyens, D., Van Herendael, H., Vandervoort, P., Pison, L.
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Published in Heart rhythm (01.09.2024)
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Predicting atrial fibrillation recurrence after catheter ablation using an artificial intelligence-enabled electrocardiogram algorithm
Gruwez, H, Barthels, M, Dhont, S, Meekers, E, Wouters, F, Pierlet, N, Nuyens, D, Rivero-Ayerza, M, Van Herendael, H, Pison, L, Haemers, P, Vandervoort, P
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GULBA, D. C, BARTHELS, M, WESTHOFF-BLECK, M, JOST, S, RAFFENBEUL, W, DANIEL, W. G, HECKER, H, LICHTLEN, P. R
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Predicting post-operative atrial fibrillation after cardiac surgery using an artificial intelligence-enabled electrocardiogram algorithm
Gruwez, H, Vandenberghe, E, Barthels, M, Vermunicht, P, Ezzat, D, Lamberigts, M, Rodrigus, I, Van Kerrebroeck, C, Pierlet, N, Heidbuchel, H, Pison, L, Rega, F, Vandervoort, P, Haemers, P
Published in Europace (London, England) (24.05.2024)
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Severe autoimmune protein S deficiency in a boy with idiopathic purpura fulminans
Bergmann, F, Hoyer, P F, D'Angelo, S V, Mazzola, G, Oestereich, C, Barthels, M, D'Angelo, A
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The use of high dose aprotinin in liver transplantation: The influence on fibrinolysis and blood loss
Grosse, H., Lobbes, W., Frambach, M., von Broen, O., Ringe, B., Barthels, M.
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Factor VIII Inhibitor–Tests Could Be Less Sensitive Than Supposed
Barthels, M., Kraus, M., Bohn, U., Liese, B., von Depka, M., Eisert, R., Ganser, A.
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Thromboembolic complications in children with nephrotic syndrome. Risk and incidence
Hoyer, P F, Gonda, S, Barthels, M, Krohn, H P, Brodehl, J
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Anticoagulant prophylaxis and therapy in patients with cancer
von Depka Prondzinski, M, Karthaus, M, Ganser, A, Barthels, M
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Clinical phenotypes and factor VII genotype in congenital factor VII deficiency
Mariani, Guglielmo, Herrmann, Falko H, Dolce, Alberto, Batorova, Angelika, Etro, Daniela, Peyvandi, Flora, Wulff, Karin, Schved, Jean F, Auerswald, Günter, Ingerslev, Jorgen, Bernardi, Francesco
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Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene
HERRMANN, F. H., WULFF, K., AUERSWALD, G., SCHULMAN, S., ASTERMARK, J., BATOROVA, A., KREUZ, W., POLLMANN, H., RUIZ-SAEZ, A., DE BOSCH, N., SALAZAR-SANCHEZ, L.
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Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene
HERRMANN, F. H., AUERSWALD, G., RUIZ-SAEZ, A., NAVARRETE, M., POLLMANN, H., LOPACIUK, S., BATOROVA, A., WULFF, K.
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Successful renal transplantation in severe von Willebrand's disease
Kliem, V, Ringe, B, Barthels, M, Frei, U, Neumann, K H
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