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Profil

Lombet Jacques

Département des sciences cliniques

See author's contact details
Main Referenced Co-authors
Collard, Laure  (4)
Cavalier, Etienne  (3)
Mekahli, Djalila (3)
Schaefer, Franz (3)
Verloes, Alain  (3)
Main Referenced Keywords
Humans (3); alopecia (2); Infant (2); rickets (2); 1 (1);
Main Referenced Disciplines
Pediatrics (10)
Urology & nephrology (6)
Genetics & genetic processes (4)
General & internal medicine (3)
Orthopedics, rehabilitation & sports medicine (2)

Publications (total 19)

The most downloaded
175 downloads
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. https://hdl.handle.net/2268/255417

The most cited

37 citations (OpenCitations)

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 https://hdl.handle.net/2268/231186

Morello, W., Baskin, E., Jankauskiene, A., Yalcinkaya, F., Zurowska, A., Puccio, G., Serafinelli, J., La Manna, A., Krzemień, G., Pennesi, M., La Scola, C., Becherucci, F., Brugnara, M., Yuksel, S., Mekahli, D., Chimenz, R., De Palma, D., Zucchetta, P., Vajauskas, D., ... PREDICT Study, G. (Other coll.). (14 September 2023). Antibiotic Prophylaxis in Infants with Grade III, IV, or V Vesicoureteral Reflux. New England Journal of Medicine, 389 (11), 987-997. doi:10.1056/NEJMoa2300161
Peer Reviewed verified by ORBi

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.
Editorial reviewed

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.
Editorial Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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.
Peer reviewed

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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).
Peer reviewed

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

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.
Peer reviewed

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.
Peer reviewed

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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
Peer Reviewed verified by ORBi

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.
Peer Reviewed verified by ORBi

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