Publications and communications of Jacques LOMBET

Guffens, A., Lombet, J., & Pirotte, I. (July 2022). Infarctus rénal chez un adolescent porteur d’un trait drépanocytaire. Revue Médicale de Liège, 77 (7-8), 448-451.

Laurent, M., De Schepper, J., Trouet, D., Godefroid, N., Boros, E., Heinrichs, C., Bravenboer, B., Velkeniers, B., Lammens, J., Harvengt, P., Cavalier, E., Kaux, J.-F., LOMBET, J., De Waele, K., Verroken, C., van Hoeck, K., Mortier, G., Levtchenko, E., & Vande Walle, J. (March 2021). Consensus Recommendations for the Diagnosis and Management of X-Linked Hypophosphatemia in Belgium. Frontiers in Endocrinology, 12, 641543. doi:10.3389/fendo.2021.641543

BOEMER, F., Caberg, J.-H., Beckers, P., Dideberg, V., di Fiore, S., Bours, V., Marie, S., Dewulf, J., Marcelis, L., Deconinck, N., Daron, A., Blasco-Perez, L., Tizzano, E., Hiligsmann, M., Lombet, J., Pereira, T., Lopez-Granados, L., Shalchian-Tehran, S., van Assche, V., ... Servais, L. (2021). Three years pilot of spinal muscular atrophy newborn screening turned into official program in Southern Belgium. Scientific Reports, 11 (1), 19922. doi:10.1038/s41598-021-99496-2

Quiros, A., LEFEBVRE, C., COLLARD, L., Rigo, V., & LOMBET, J. (July 2020). Syndrome néphrotique congénital sévère avec mutation NPH S1. Revue Médicale de Liège, 75 (7-8), 544-547.

De Rechter, S., Bockenhauer, D., Guay-Woodford, L. M., Liu, I., Mallett, A. J., Soliman, N. A., Sylvestre, L. C., Schaefer, F., Liebau, M. C., Mekahli, D., Adamczyk, P., Akinci, N., Alpay, H., Ardelean, C., Ayasreh, N., Aydin, Z., Bael, A., Baudouin, V., Bayrakci, U. S., ... Zachwieja, K. (29 May 2019). ADPedKD: A Global Online Platform on the Management of Children With ADPKD. Kidney International Reports, 4 (9), 1271-1284. doi:10.1016/j.ekir.2019.05.015

Boodhoo, F. M., BARREA, C., Lombet, J., & Seghaye, M.-C. (March 2018). Stunted growth and alopecia totalis: A case report. Belgian Journal of Paediatrics, 20 (1).

D'OTREPPE DE BOUVETTE, S., Lombet, J., Tebache, M., CABERG, J.-H., & BULK, S. (16 February 2018). Another case of Galloway-Mowat syndrome associated with a biallelic mutation of the OSGEP gene [Poster presentation]. Meeting of the Belgian Society for Human Genetics (BeSHG) : "The Epigenome in development and disease", Ghent, Belgium.

DACHY, A., EIRAS DA SILVA, S., THELEN, A., COLLARD, L., GHUYSEN, M.-S., LOMBET, J., MAQUET, J., & PHILIPPET, P. (19 May 2016). Oral treatment of febrile urinary tract infection in children: Feasibility and follow-up. Archives de Pédiatrie, 23 (6), 642-643. doi:10.1016/j.arcped.2016.03.046

Davin, J.-C., Dechenne, C., Lombet, J., Rentier, B., Foidart, J. B., & Mahieu, P. R. (1989). Acute experimental glomerulonephritis induced by the glomerular deposition of circulating polymerid IgA-Concanavalin A complexes. Virchows Archiv. A: Pathological Anatomy and Histopathology, 415 (1), 7-20.