Kastrissianakis, K., Bouvy, A.-F., Goetghebuer, T., Melice, N., Michel, M., Kadz, E., Pieltain, C., Sonck, T., Lannoo, P., & Lombet, J. (January 2023). Impact of the COVID-19 pandemic on early childhood preventive care activities of Office de la Naissance et de l'Enfance (ONE). Belgian Journal of Paediatrics, 23 (4), 281-286. |
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. R., 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. R., Levtchenko, E., & Vande Walle, J. (May 2021). Corrigendum: Consensus Recommendations for the Diagnosis and Management of X-Linked Hypophosphatemia in Belgium. Frontiers in Endocrinology, 12, 686401. doi:10.3389/fendo.2021.686401 |
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 |
Nicolescu, C. R., Lombet, J., & Cavalier, E. (November 2018). Vitamin D-Resistant Rickets and Cinacalcet-One More Favorable Experience. Frontiers in Pediatrics, 6, 376. doi:10.3389/fped.2018.00376 |
Burgmaier, K., Kunzmann, K., Ariceta, G., Bergmann, C., Buescher, A. K., Burgmaier, M., Dursun, I., Duzova, A., Eid, L., Erger, F., Feldkoetter, M., Galiano, M., Gessner, M., Goebel, H., Gokce, I., Haffner, D., Hooman, N., Hoppe, B., Jankauskiene, A., ... COLLARD, L. (August 2018). Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease. Journal of Pediatrics, 199, 22-28.e6. doi:10.1016/j.jpeds.2018.03.052 |
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 |
Nyamugabo, K., Poirrier, A.-L., Spote, V., Moreau, P., & Lombet, J. (January 2008). L'image du mois. Un accessoire de Noel bien encombrant. Revue Médicale de Liège, 63 (1), 56. |
De Halleux, V., Lombet, J., & Rigo, J. (2007). Prevention de l'infection respiratoire a VRS par immunoglobulines monoclonales specifiques (palivizumab, Synagis). Revue Médicale de Liège, 62 (5-6, May-Jun), 299-302. |
Verloes, A., Raoul, M., Genevieve, D., Sznajer, Y., Demarche, M., Lombet, J., Rigo, V., Misson, J.-P., Collignon, L., Vanwijck, F., & Vanwijck, R. (October 2004). Bony syngnathia, vertebral segmentation defect, coloboma, microcephaly and mental retardation: confirmation of Dobrow syndrome and review of syndromal syngnathias. Clinical Dysmorphology, 13 (4), 205-211. doi:10.1097/00019605-200410000-00002 |
Verloes, A., Hermanns-Le, T., Lesenfants, S., Lombet, J., Lamotte, P. J., Crevecoeur-Liegeois, C., Duchesne, B., & Pierard, G. (29 October 1999). Koraxitrachitic Syndrome: A Syndromic Form of Self-Healing Collodion Baby with Residual Dappled Atrophy of the Derma. American Journal of Medical Genetics, 86 (5), 454-8. doi:10.1002/(SICI)1096-8628(19991029)86:5<454::AID-AJMG11>3.0.CO;2-U |
Herens, C., Jamar, M., Alvarez Gonzalez, M.-L., Lesenfants, S., Lombet, J., Bonnivert, J., Koulischer, L., & Verloes, A. (12 December 1997). Private Multiple Congenital Anomaly Syndromes May Result from Unbalanced Subtle Translocations: T(2q;4p) Explains the Lambotte Syndrome. American Journal of Medical Genetics, 73 (2), 127-31. doi:10.1002/(SICI)1096-8628(19971212)73:2<127::AID-AJMG5>3.0.CO;2-R |
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. |