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1. • 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)
2. • 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)
3. • 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)
4. • Journal article

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   Clinical characteristics and outcomes of children with stage 3-5 chronic kidney disease.

   Tran, Thi Mong Hiep Ismaili, Khalid Collart, Frederic Van Damme-Lombaerts, Rita Godefroid, Nathalie[UCL] Ghuysen, Marie-Sophie Van Hoeck, Koen Raes, Ann Janssen, Françoise Robert, Annie[UCL] (2010) Pediatric Nephrology — Vol. 25, no. 5, p. 935-940 (2010)
5. • 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)
6. • Journal article

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   Typical or Atypical Hemolytic Uremic Syndrome and the Use of Eculizumab: 4 Illustrative Cases.

   de Ville de Goyet, Maëlle[UCL] Detaille, Thierry[UCL] Godefroid, Nathalie[UCL] (2019) Journal of pediatric hematology/oncology — Vol. 41, no. 7, p. e459-e462 (2019)
7. • Journal article

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   Sclérose tubéreuse de Bourneville: poser le diagnostic et traiter à bon escient

   Pirson, Yves[UCL] Ho, Thien Anh[UCL] Demoulin, Nathalie[UCL] Godefroid, Nathalie[UCL] Dekeuleneer, Valérie[UCL] Van Rijckevorsel, Germaine[UCL] Nassogne, Marie-Cécile[UCL] El Tahry, Riëm[UCL] Sznajer, Yves[UCL] (2017) Louvain médical — Vol. janvier, p. 10-15 (2017)
8. • Speech

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   The many faces of atypical Hemolytic Uremic Syndrome (aHUS) in Belgium

   Massart, Annick Claes, Kathleen Weekers, Laurent Broeders, Nilufer Goffin, Eric[UCL] Adams, Brigitte Bosmans, Jean-Louis Collard, Laure Levtchencko, Elena Pipeleers, Lissa Van Hoeck, Koen Abramowicz, Daniel Nortier, Joëlle Nikolaou, Vasilis Hilbert, Pascale Dahan, Karin Stordeur, Patrick Godefroid, Nathalie[UCL] Vande Walle, Johann (2018) 23rd Annual Congress of the Belgian Society of Internal Medicine — La Hulpe, Belgium
9. • 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)
10. • Journal article

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    Risk Factors for Early Dialysis Dependency in Autosomal Recessive Polycystic Kidney Disease.

    Burgmaier, Kathrin Kunzmann, Kevin Ariceta, Gema Bergmann, Carsten Buescher, Anja Katrin Burgmaier, Mathias Dursun, Ismail Duzova, Ali Eid, Loai Erger, Florian Feldkoetter, Markus Galiano, Matthias Geßner, Michaela Goebel, Heike Gokce, Ibrahim Haffner, Dieter Hooman, Nakysa Hoppe, Bernd Jankauskiene, Augustina Klaus, Guenter König, Jens Litwin, Mieczyslaw Massella, Laura Mekahli, Djalila Melek, Engin Mir, Sevgi Pape, Lars Prikhodina, Larisa Ranchin, Bruno Schild, Raphael Seeman, Tomas Sever, Lale Shroff, Rukshana Soliman, Neveen A Stabouli, Stella Stanczyk, Malgorzata Tabel, Yilmaz Taranta-Janusz, Katarzyna Testa, Sara Thumfart, Julia Topaloglu, Rezan Weber, Lutz Thorsten Wicher, Dorota Wühl, Elke Wygoda, Simone Yilmaz, Alev Zachwieja, Katarzyna Zagozdzon, Ilona Zerres, Klaus ESCAPE Study Group GPN Study Group Dötsch, Jörg Schaefer, Franz Liebau, Max Christoph ARegPKD consortium Ranguelov, Nadejda[UCL] Godefroid, Nathalie[UCL] (2018) The Journal of pediatrics — Vol. 199, p. 22-28.e6 (2018)
11. • Journal article

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    HNF1ß: A gene, several phenotypes

    Ho, Thien Anh[UCL] Godefroid, Nathalie[UCL] Devuyst, Olivier[UCL] Pirson, Yves[UCL] Demaret, Tanguy[UCL] Dahan, Karin[UCL] (2014) Louvain médical — Vol. 133, no. 4, p. 197-200 (2014)
12. • Journal article

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    Consensus Recommendations for the Diagnosis and Management of X-Linked Hypophosphatemia in Belgium

    Laurent, Michaël R. De Schepper, Jean Trouet, Dominique Godefroid, Nathalie[UCL] Boros, Emese Heinrichs, Claudine Bravenboer, Bert Velkeniers, Brigitte Lammens, Johan Harvengt, Pol Cavalier, Etienne Kaux, Jean-François Lombet, Jacques De Waele, Kathleen Verroken, Charlotte van Hoeck, Koenraad Mortier, Geert R. Levtchenko, Elena Vande Walle, Johan (2021) Frontiers in endocrinology — Vol. 12, p. 641543 [1-20] (2021)
13. • Journal article

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    ADPedKD: A Global Online Platform on the Management of Children With ADPKD.

    De Rechter, Stéphanie Bockenhauer, Detlef Guay-Woodford, Lisa M Liu, Isaac Mallett, Andrew J Soliman, Neveen A Sylvestre, Lucimary C Schaefer, Franz Liebau, Max C Mekahli, Djalila ADPedKD Consortium Godefroid, Nathalie[UCL] Ranguelov, Nadejda[UCL] (2019) Kidney international reports — Vol. 4, no.9, p. 1271-1284 (2019)
14. • Journal article

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    Two-step transplantation for primary hyperoxaluria: Cadaveric liver followed by living donor related kidney transplantation

    Malla, Ivone Lysy, Philippe[UCL] Godefroid, Nathalie[UCL] Smets, Françoise[UCL] Malaise, Jacques Reding, Raymond[UCL] Sokal, Etienne[UCL] (2008) Pediatric Transplantation — Vol. 13, no. 6, p. 782-784 (2009)
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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    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)
17. • Journal article

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    Genotype and Outcome After Kidney Transplantation in Alport Syndrome.

    Gillion, Valentine[UCL] Dahan, Karin[UCL] Cosyns, Jean-Pierre[UCL] Hilbert, Pascale Jadoul, Michel[UCL] Goffin, Eric[UCL] Godefroid, Nathalie[UCL] De Meyer, Martine[UCL] Mourad, Michel[UCL] Pirson, Yves[UCL] Kanaan, Nada[UCL] (2018) Kidney International Reports — Vol. 3, no. 3, p. 652-660 (2018)
18. • Journal article

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    Development of renal and iliac anevrysms in a child with generalized infantile myofibromatosis

    Brasseur, Benoît[UCL] Chantrain, Christophe[UCL] Godefroid, Nathalie[UCL] Sluysmans, Thierry[UCL] Anslot, Christine[UCL] Menten, Renaud[UCL] Clapuyt, Philippe[UCL] Dupont, Sophie[UCL] Vermylen, Christiane[UCL] Brichard, Bénédicte[UCL] (2010) Pediatric Nephrology — Vol. 25, no. 5, p. 983-986 (2009)
19. • Journal article

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    vWFpp/ADAMTS13 ratio is a useful marker of postliver transplantation thrombotic microangiopathy: A pediatric case report

    Duquenne, Lisa[UCL] Balbeur, Samuel[UCL] Everard, Emilie[UCL] Reding, Raymond[UCL] Eeckhoudt, Stéphane[UCL] Brichard, Bénédicte[UCL] Godefroid, Nathalie[UCL] Derycke, Emilien[UCL] Komuta, Mina[UCL] Scheers, Isabelle[UCL] Smets, Françoise[UCL] Sokal, Etienne[UCL] Stéphenne, Xavier[UCL] (2019) Clinical Case Reports — (2019)
20. • Journal article

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    Corticosteroid-Free Kidney Transplantation Improves Growth: 2-Year Follow-up of the TWIST Randomized Controlled Trial

    Webb, Nicholas J A Douglas, Sarah E Rajai, Azita Roberts, Stephen A Grenda, Ryszard Marks, Stephen D Watson, Alan R Fitzpatrick, Maggie Vondrak, Karel Maxwell, Heather Jaray, Jeno Van Damme-Lombaerts, Rita Milford, David V Godefroid, Nathalie[UCL] Cochat, Pierre Ognjanovic, Milos Murer, Luisa McCulloch, Mignon Tönshoff, Burkhard (2015) Transplantation — Vol. 99, no. 6, p. 1178-1185 (2015)
21. • 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)
22. • 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)
23. • 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)
24. • Journal article

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    18F-Fluorodeoxyglucose Positron Emission Tomography: a Useful Tool for the Diagnosis of Endocarditis in a Boy with Congenital Heart Disease: a Case Report

    Balligand, Elise[UCL] Rojas , Cielo[UCL] Themelin, Céline[UCL] Van Houtte, Laetitia[UCL] Van der Linden, Dimitri[UCL] Roelants, Véronique[UCL] Baldin, Pamela[UCL] Godefroid, Nathalie[UCL] Poncelet, Alain[UCL] Vo, Christophe[UCL] (2021) SN Comprehensive Clinical Medicine — Vol. 3, p. 2016-2020 (2021)
25. • Journal article

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    Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations.

    Godefroid, Nathalie[UCL] Dahan, Karin[UCL] (2010) Nephrology, Dialysis, Transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association — Vol. 25, no. 9, p. 2837-2839 (2010)

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