Articles dans des revues avec comité de lecture (17)

  1. 1. Jacobs, L., Taghavi, M., Fallas, J., Geers, C., Libertalis, M., Smet, J., Nortier, J., & Mesquita, M. (2024). Multisystemic Beryllium Disease: An Exceptional Case Revealed by a Urinary Tract Granulomatosis. International Journal of Molecular Sciences (CD-ROM), 25(15), 8166. doi:10.3390/ijms25158166
  2. 2. Akiki, P., Dedeken, L., Ferster, A., Doyen, V., Dupire, G., Nagant, C., Smet, J., Ghorra, N., Ruth, I., Lauwers, M., Daubie, V., Corazza, F., & El Kenz, H. (2023). Pilot study on the use of basophil activation tests and skin tests for the prevention of allergic transfusion reactions. Frontiers in Allergy, 4, 1328227. doi:10.3389/falgy.2023.1328227
  3. 3. Ponthieux, F., Dauby, N., Maillart, E., Fils, J.-F., Smet, J., Claus, M., Besse-Hammer, T., De Bels, D., Corazza, F., & Nagant, C. (2022). Tocilizumab-Induced Unexpected Increase of Several Inflammatory Cytokines in Critically Ill COVID-19 Patients: The Anti-Inflammatory Side of IL-6. Viral immunology. doi:10.1089/vim.2021.0111
  4. 4. Naesens, L., Smet, J., Tavernier, S. S., Schelstraete, P., Hoste, L., Lambrecht, S., Verhelst, H., van der Werff Ten Bosch, J., Ferster, A., Blumental, S., Hilbert, P., Kerre, T., Schurmans, T., Licht, C., Roumenina, L. L., Stordeur, P., & Haerynck, F. (2020). Plasma C3d levels as a diagnostic marker for complete complement factor I deficiency. Journal of allergy and clinical immunology. doi:10.1016/j.jaci.2020.08.014
  5. 5. Nagant, C., Ponthieux, F., Smet, J., Dauby, N., Doyen, V., Besse-Hammer, T., De Bels, D., Maillart, E., & Corazza, F. (2020). A score combining early detection of cytokines accurately predicts COVID-19 severity and intensive care unit transfer. International journal of infectious diseases. doi:10.1016/j.ijid.2020.10.003
  6. 6. Cremer, A., Ku, J., Amininejad, L., Bouvry, M. R., Brohet, F., Liefferinckx, C., Devière, J., Van Gossum, A., Smet, J., Stordeur, P., & Franchimont, D. (2019). Variability of faecal calprotectin in inflammatory bowel disease patients: An observational case-control study. Journal of Crohn's and Colitis, 13(11), 1372-1379. doi:10.1093/ecco-jcc/jjz069
  7. 7. La, C., Stordeur, P., Smet, J., Franchimont, D., Lauwerys, B. B., Lê, P. Q., Goffin, L., Boulanger, C., Ferster, A., Brasseur, J. P., Brasseur, B., Tuerlinckx, D., Spruyt, D., Rasschaert, J., De Maertelaer, V., Kleimberg, S., Sokolova, T., Durez, P., & Badot, V. (2016). Place du dosage de la calprotectine sérique comme biomarqueur d'intérêt dans l'arthrite juvénile idiopathique. Revue du rhumatisme, 83, A60-A61. doi:10.1016/S1169-8330(16)30246-0
  8. 8. Arget, M., Smet, J., & Soyfoo, M. S. (2016). Facteurs anti-nucléaires " non-identifiés " dans la sclérodermie systémique. Revue médicale de Bruxelles, 37(5), 401-407.
  9. 9. De Schutter, I., Vergison, A., Tuerlinckx, D., Raes, M., Smet, J., Smeesters, P., Verhaegen, J., Mascart, F., Surmont, F., & Malfroot, A. (2014). Pneumococcal aetiology and serotype distribution in paediatric community-acquired pneumonia. PloS one, 9(2), e89013. doi:10.1371/journal.pone.0089013
  10. 10. Smits, K., Pottier, G., Smet, J., Dirix, V., Vermeulen, F., De Schutter, I., Carollo, M., Locht, C., Ausiello, C. M., & Mascart, F. (2013). Different T cell memory in preadolescents after whole-cell or acellular pertussis vaccination. Vaccine, 32(1), 111-118. doi:10.1016/j.vaccine.2013.10.056
  11. 11. Tuerlinckx, D., Smet, J., De Schutter, I., Jamart, J., Vergison, A., Raes, M., Smeesters, P., Verhaegen, J., Surmont, F., Malfroot, A., & Mascart, F. (2013). Evaluation of a WHO-Validated Serotype-Specific Serological Assay for the Diagnosis of Pneumococcal Etiology in Children with Community-Acquired Pneumonia. The Pediatric infectious disease journal, 32(7), 277-84. doi:10.1097/INF.0b013e31828c363f
  12. 12. Vilain, C., Rens, C., Aeby, A., Balériaux, D., Van Bogaert, P., Remiche, G., Smet, J., Van Coster, R., Abramowicz, M., & Pirson, I. (2011). A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome. Clinical genetics, 82(3), 264-270. doi:10.1111/j.1399-0004.2011.01743.x

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