Publications and communications of Jacques LOMBET

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 session presented at 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.