All Publications

Pages

1. • Journal article

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   Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome.

   Riveira-Munoz, Eva[UCL] Chang, Qing Godefroid, Nathalie[UCL] Hoenderop, Joost G. Bindels, René J Dahan, Karin[UCL] Devuyst, Olivier[UCL] (2007) Journal of the American Society of Nephrology : JASN — Vol. 18, no. 4, p. 1271-83 (2007)
2. • Journal article

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   A girl with rickets and nephrocalcinosis

   Godefroid, Nathalie[UCL] Proesmans, W. (2003) Pediatric Nephrology — Vol. 18, no. 6, p. 573-575 (2003)
3. • Speech

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   Syndrome de Gitelman et protéinurie glomérulaire: à propos d'une association atypique

   Demoulin, Nathalie[UCL] Cosyns, Jean-Pierre[UCL] Cornet, C. Godefroid, Nathalie[UCL] Pirson, Yves[UCL] Jadoul, Michel[UCL] Dahan, Karin[UCL] Devuyst, Olivier[UCL] (2010) 12e Réunion commune de la Société de Néphrologie (SN) et de la Société Francophone de Dialyse (SFD) — (Belgium) Brussels
4. • Journal article

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   Les inhibiteurs mTOR : nouvel outil thérapeutique dans la prise en charge de la Sclérose Tubéreuse de Bourneville. Expérience de l’équipe multidisciplinaire des Cliniques universitaires Saint-Luc

   Dekeuleneer, Valérie[UCL] Ho, Thien Anh[UCL] Van Rijckevorsel, Germaine[UCL] Sznajer, Yves[UCL] Nassogne, Marie-Cécile[UCL] Godefroid, Nathalie[UCL] Derouaux, Anne-Sophie[UCL] Pirson, Yves[UCL] (2015) Louvain médical — Vol. 134, no.10, p. 537-546 (2015)
5. • Journal article

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   Genetic investigation of autosomal recessive distal renal tubular acidosis: Evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene

   Vargas-Poussou, R Godefroid, Nathalie[UCL] (2006) Journal of the American Society of Nephrology — Vol. 17, no. 5, p. 1437-1443 (2006)
6. • Speech

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   A new class of mutations involved in Gitelman's syndrome affects the intrinsic activity of the Na-Cl cotransporter NCCT

   Riveira-Munoz, Eva[UCL] Dahan, Karin[UCL] Godefroid, Nathalie[UCL] Devuyst, Olivier[UCL] Chang, Qing Hoenderop, Joost G. Bindels, Rene (2006) 43rd ERA-EDTA Congress — Glasgow (Scotland)
7. • Journal article

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   A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension.

   Godefroid, Nathalie Riveira-Munoz, Eva[UCL] Saint-Martin, Christine Nassogne, Marie-Cécile[UCL] Dahan, Karin[UCL] Devuyst, Olivier[UCL] (2006) American journal of kidney diseases : the official journal of the National Kidney Foundation — Vol. 48, no. 5, p. e73-9 (2006)
8. • Journal article

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   INNOVATIONS EN Néphrologie QUE RETENIR DE 2016 ?

   Demoulin, Nathalie[UCL] Anh Ho[UCL] Godefroid, Nathalie[UCL] Clerckx Caroline[UCL] Annet, Laurence[UCL] Pirson, Yves[UCL] Devuyst, Olivier[UCL] Jadoul, Michel[UCL] Aydin, Selda[UCL] Goletti Sylvie[UCL] Morelle, Johann[UCL] Goffin, Eric[UCL] Mourad, Michel[UCL] (2017) Louvain médical — Vol. 136, no.2, p. 103-109 (2017)
9. • Journal article

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   Révolution thérapeutique en cours dans l’hyperoxalurie primaire de type 1

   Devresse, Arnaud[UCL] Godefroid, Nathalie[UCL] Kanaan, Nada[UCL] (2021) Louvain médical — Vol. mars, no.140, p. 166-171 (2021)
10. • Journal article

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    Liver Transplantation in Primary Hyperoxaluria Type 1: We Have to Find an Alternative!

    Devresse, Arnaud[UCL] Godefroid, Nathalie[UCL] Anthonissen, Blaise[UCL] Labriola, Laura[UCL] De Magnee, Catherine[UCL] Reding, Raymond[UCL] Sokal, Etienne[UCL] Stéphenne, Xavier[UCL] Gillion, Valentine[UCL] Kanaan, Nada[UCL] (2021) Transplantation — Vol. 105, no. 4, p. e46-e47 (2021)
11. • Journal article

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    Low rates of humoral response to BNT162b2 SARS-CoV-2 vaccination in patients with immune-mediated kidney diseases treated with rituximab.

    Demoulin, Nathalie[UCL] Scohy, Anaïs[UCL] Gillion, Valentine[UCL] Godefroid, Nathalie[UCL] Jadoul, Michel[UCL] Morelle, Johann[UCL] (2021) Clinical kidney journal — Vol. 14, no. 9, p. 2132-2133 (2021)
12. • Journal article

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    Characterization, evolution and risk factors of diabetes and prediabetes in a pediatric cohort of renal and liver transplant recipients

    Welsch, Sophie Mailleux, Virginie le Hardy de Beaulieu, Priscilla Ranguelov, Nadejda Godefroid, Nathalie Robert, Annie Stéphenne, Xavier[UCL] Scheers, Isabelle[UCL] Reding, Raymond Sokal, Etienne[UCL] Lysy, Philippe A. (2023) Frontiers in Pediatrics — Vol. 11 (2023)
13. • Journal article

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    Epidemiology, Outcomes, and Complement Gene Variants in Secondary Thrombotic Microangiopathies.

    Wérion, Alexis[UCL] Storms, Pauline Zizi, Ysaline Beguin, Claire[UCL] Bernards, Jelle Cambier, Jean-François Dahan, Karin Dierickx, Daan Godefroid, Nathalie[UCL] Hilbert, Pascale Lambert, Catherine[UCL] Levtchenko, Elena Meyskens, Thomas Poiré, Xavier van den Heuvel, Lambert Claes, Kathleen J Morelle, Johann[UCL] UCLouvain TMA/HUS Network and KU Leuven TMA/HUS Network Aydin, Selda[UCL] Demoulin, Nathalie[UCL] Devresse, Arnaud[UCL] Gillion, Valentine[UCL] Goffin, Eric[UCL] Jadoul, Michel[UCL] Kanaan, Nada[UCL] Labriola, Laura[UCL] Pirson, Yves[UCL] Ranguelov, Nadejda[UCL] Van Regemorter, Elliott[UCL] Wittebole, Xavier[UCL] Hantson, Philippe[UCL] Pochet, Jean-Michel[UCL] (2023) Clinical journal of the American Society of Nephrology : CJASN — Vol. 18, no.7, p. 881-891 (2023)
14. • Journal article

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    mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy

    Schlingmann, Karl P. Jouret, François Shen, Kuang Nigam, Anukrati Arjona, Francisco J. Dafinger, Claudia Houillier, Pascal Jones, Deborah P. Kleinerüschkamp, Felix Oh, Jun Godefroid, Nathalie[UCL] Eltan, Mehmet Güran, Tülay Burtey, Stéphane Parotte, Marie-Christine König, Jens Braun, Alina Bos, Caro Ibars Serra, Maria Rehmann, Holger Zwartkruis, Fried J.T. Renkema, Kirsten Y. Klingel, Karin Schulze-Bahr, Eric Schermer, Bernhard Bergmann, Carsten Altmüller, Janine Thiele, Holger Beck, Bodo B. Dahan, Karin[UCL] Sabatini, David Liebau, Max C. Vargas-Poussou, Rosa Knoers, Nine V.A.M. Konrad, Martin de Baaij, Jeroen H.F. (2021) Journal of the American Society of Nephrology — Vol. 32, no. 11, p. 2885-2899 (2021)
15. • Journal article

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    La néphrologie pédiatrique du rein foetal au rein greffé

    Hall, Michelle Janssen, Fanny De Pauw, Luc[UCL] Hooghe, L. Schurmans, T. Adams, B. Godefroid, Nathalie[UCL] Lolin, K. Ismaili, K. (2008) Revue médicale de Bruxelles — Vol. 29, no. Suppl 1, p. S25-S31 (2008)
16. • Journal article

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    Kidney Versus Combined Kidney and Liver Transplantation in Young People With Autosomal Recessive Polycystic Kidney Disease: Data From the European Society for Pediatric Nephrology/European Renal Association-European Dialysis and Transplant (ESPN/ERA-EDTA) Registry.

    Mekahli, Djalila van Stralen, Karlijn J Bonthuis, Marjolein Jager, Kitty J Balat, Ayşe Benetti, Elisa Godefroid, Nathalie[UCL] Edvardsson, Vidar O Heaf, James G Jankauskiene, Augustina Kerecuk, Larissa Marinova, Svetlana Puteo, Flora Seeman, Tomas Zurowska, Aleksandra Pirenne, Jacques Schaefer, Franz Groothoff, Jaap W ESPN/ERA-EDTA Registry (2016) American Journal of Kidney Diseases — Vol. 68, no. 5, p. 782-788 (2016)
17. • Journal article

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    Belgian consensus statement on the diagnosis and management of patients with atypical hemolytic uremic syndrome

    Claes, Kathleen Massart, Annick Collard, Laure Weekers, Laurent Goffin, Eric[UCL] Pochet, Jean-Michel[UCL] Dahan, Karin[UCL] Morelle, Johann[UCL] Adams, Brigitte Broeders, Nilufer Stordeur, Patrick Abramowicz, Daniel Bosmans, Jean-Louis Van Hoeck, Koen Janssens, Peter Pipeleers, Lissa Peeters, Patrick Van Laecke, Steven Levtchenko, Elena Sprangers, Ben van den Heuvel, Lambertus Godefroid, Nathalie[UCL] Van de Walle, Johan (2018) Acta Clinica Belgica — Vol. 73, no. 1, p. 80-89 (2018)
18. • Journal article

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    Kidney transplantation in infantile myofibromatosis and fibromuscular dysplasia: a case report.

    FREZIN, Julie[UCL] Fusaro, Fabio[UCL] Reding, Raymond[UCL] Godefroid, Nathalie[UCL] (2015) Journal of Medical Case Reports — Vol. 9, no.1, p. 270 (2015)
19. • Journal article

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    46 XX-Females affected by WT1 splice site mutations in intron 9 (Frasier site) have a conserved reproductive function

    Godefroid, Nathalie[UCL] Goffin, Eric[UCL] Aydin, Selda[UCL] Dahan, Karin[UCL] (2015) J Med Genet — Vol. N/D, no.N/D, p. N/D (N/D)
20. • Journal article

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    Accumulation of uraemic toxins is reflected only partially by estimated GFR in paediatric patients with chronic kidney disease.

    Snauwaert, Evelien Van Biesen, Wim Raes, Ann Holvoet, Els Glorieux, Griet Van Hoeck, Koen Van Dyck, Maria Godefroid, Nathalie[UCL] Vanholder, Raymond Roels, Sanne Walle, Johan Vande Eloot, Sunny (2018) Pediatric Nephrology — Vol. 33, no.2, p. 315-323 (2018)
21. • Journal article

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    Autosomal dominant polycystic kidney disease is associated with central and nephrogenic defects in osmoregulation.

    Ho, Thien Anh[UCL] Godefroid, Nathalie[UCL] Gruzon, Damien[UCL] Haymann, Jean-Philippe Maréchal, Céline[UCL] Wang, Xueqi Serra, Andreas Pirson, Yves[UCL] Devuyst, Olivier[UCL] (2012) Kidney International — Vol. 82, no. 10, p. 1121-1129 (2012)
22. • Journal article

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    Fewer pre-emptive renal transplantations and more rejections in immigrant children compared to native Dutch and Belgian children.

    Tromp, Wilma F Cransberg, Karlien van der Lee, Johanna H Bouts, Antonia H Collard, Laure Van Damme-Lombaerts, Rita Godefroid, Nathalie[UCL] Van Hoeck, Koenraad J Koster-Kamphuis, Linda Lilien, Marc R Raes, Ann Ranguelov, Nadejda Groothoff, Jaap W (2012) Nephrology, Dialysis, Transplantation — Vol. 27, no.6, p. 2588-2593 (2012)
23. • Journal article

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    Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies

    Ashton, Emma J. Legrand, Anne Benoit, Valerie Roncelin, Isabelle Venisse, Annabelle Zennaro, Maria-Christina Jeunemaitre, Xavier Iancu, Daniela van’t Hoff, William G. Walsh, Stephen B. Godefroid, Nathalie[UCL] Rotthier, Annelies Del Favero, Jurgen Devuyst, Olivier[UCL] Schaefer, Franz Jenkins, Lucy A. Kleta, Robert Dahan, Karin[UCL] Vargas-Poussou, Rosa Bockenhauer, Detlef (2018) Kidney international — Vol. 93, no. 4, p. 961-967 (2018)
24. • Journal article

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    Transplantation for Primary Hyperoxaluria Type 1: Designing New Strategies in the Era of Promising Therapeutic Perspectives.

    Devresse, Arnaud[UCL] Cochat, Pierre Godefroid, Nathalie[UCL] Kanaan, Nada[UCL] (2020) Kidney international reports — Vol. 5, no. 12, p. 2136-2145 (2020)
25. • Journal article

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    Cinacalcet sustainedly prevents pancreatitis in a child with a compound heterozygous SPINK1/AP2S1 mutation

    Scheers, Isabelle[UCL] Sokal, Etienne[UCL] Limaye, Nisha[UCL] Denoncin, Catherine Stephenne, Xavier[UCL] Pirson, Yves[UCL] Godefroid, Nathalie[UCL] (2019) Pancreatology — Vol. 19, no. 6, p. 801-804 (2019)

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