Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies von Debiec, Hanna, Nauta, Jeroen, Coulet, Florence, van der Burg, Mirjam, Guigonisy, Vincent, Schurmans, Thierry, de Heer, Emile, Soubrier, Florent, Janssen, Francoise, Ronco, Pierre

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CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency von van Zelm, Menno C, Smet, Julie, Adams, Brigitte, Mascart, Françoise, Schandené, Liliane, Janssen, Françoise, Ferster, Alina, Kuo, Chiung-Chi, Levy, Shoshana, van Dongen, Jacques J M, van der Burg, Mirjam

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Predicting the Clinical Outcome of Antenatally Detected Unilateral Pelviureteric Junction Stenosis von Duong, Hong Phuoc, Piepsz, Amy, Collier, Frank, Khelif, Karim, Christophe, Catherine, Cassart, Marie, Janssen, Françoise, Hall, Michelle, Ismaili, Khalid

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Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome von Harambat, Jérôme, Fargue, Sonia, Acquaviva, Cécile, Gagnadoux, Marie-France, Janssen, Françoise, Liutkus, Aurélia, Mourani, Chebl, Macher, Marie-Alice, Abramowicz, Daniel, Legendre, Christophe, Durrbach, Antoine, Tsimaratos, Michel, Nivet, Hubert, Girardin, Eric, Schott, Anne-Marie, Rolland, Marie-Odile, Cochat, Pierre

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Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectrum von Matejas, Verena, Hinkes, Bernward, Alkandari, Faisal, Al-Gazali, Lihadh, Annexstad, Ellen, Aytac, Mehmet B., Barrow, Margaret, Bláhová, Květa, Bockenhauer, Detlef, Cheong, Hae Il, Maruniak-Chudek, Iwona, Cochat, Pierre, Dötsch, Jörg, Gajjar, Priya, Hennekam, Raoul C., Janssen, Françoise, Kagan, Mikhail, Kariminejad, Ariana, Kemper, Markus J., Koenig, Jens, Kogan, Jillene, Kroes, Hester Y., Kuwertz-Bröking, Eberhard, Lewanda, Amy F., Medeira, Ana, Muscheites, Jutta, Niaudet, Patrick, Pierson, Michel, Saggar, Anand, Seaver, Laurie, Suri, Mohnish, Tsygin, Alexey, Wühl, Elke, Zurowska, Aleksandra, Uebe, Steffen, Hildebrandt, Friedhelm, Antignac, Corinne, Zenker, Martin

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Transverse comparisons between ultrasound and radionuclide parameters in children with presumed antenatally detected pelvi-ureteric junction obstruction von Duong, Hong Phuoc, Piepsz, Amy, Khelif, Karim, Collier, Frank, de Man, Kathia, Damry, Nash, Janssen, Françoise, Hall, Michelle, Ismaili, Khalid

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Genetic forms of nephrotic syndrome: a single-center experience in Brussels von Wissing, Karl Martin, Janssen, Francoise, Pawtowski, Audrey, Boyer, Olivia, Ismaili, Khalid, Hall, Michelle

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Clinical characteristics and outcomes of children with stage 3–5 chronic kidney disease von Mong Hiep, Tran Thi, Ismaili, Khalid, Collart, Frederic, Van Damme-Lombaerts, Rita, Godefroid, Nathalie, Ghuysen, Marie-Sophie, Van Hoeck, Koen, Raes, Ann, Janssen, Françoise, Robert, Annie

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Genetic forms of nephrotic syndrome: a single-center experience in Brussels von Ismaili, Khalid, Wissing, Karl Martin, Janssen, Françoise, Hall, Michelle

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Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1 von Fargue, Sonia, Harambat, Jérôme, Gagnadoux, Marie-France, Tsimaratos, Michel, Janssen, Françoise, Llanas, Brigitte, Berthélémé, Jean-Pierre, Boudailliez, Bernard, Champion, Gérard, Guyot, Claude, Macher, Marie-Alice, Nivet, Hubert, Ranchin, Bruno, Salomon, Rémi, Taque, Sophie, Rolland, Marie-Odile, Cochat, Pierre

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Neonatal disease in neutral endopeptidase alloimmunization: lessons for immunological monitoring von Nortier, Joëlle L, Debiec, Hanna, Tournay, Yasmina, Mougenot, Beatrice, Nöel, Jean-Christophe, Deschodt-Lanckman, Monique M, Janssen, Françoise, Ronco, Pierre

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Epidemiological urinalysis of children from kindergartens of Can Gio, Ho Chi Minh City - Vietnam von Dang, Le Nhu Nguyet, Doan, Thi Le Binh, Doan, Ngoc Hue, Pham, Thi Kim Hoa, Smets, Françoise, Thi, Mong Hiep Tran, Janssen, Françoise, Robert, Annie

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Hereditary polycystic kidney diseases in children: changing sonographic patterns through childhood von AVNI, Fred E, GUISSARD, Gretel, HALL, Michelle, JANSSEN, Francoise, DEMAERTELAER, Viviane, RYPENS, Francoise

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Etiology and outcome of chronic renal failure in hospitalized children in Ho Chi Minh City, Vietnam von Mong Hiep, Tran Thi, Janssen, Françoise, Ismaili, Khalid, Khai Minh, Dang, Vuong Kiet, Doan, Robert, Annie

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WT1 gene mutations in three girls with nephrotic syndrome von Ismaili, Khalid, Verdure, Véronique, Vandenhoute, Katherina, Janssen, Françoise, Hall, Michelle

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Multicentre prospective randomised trial of tacrolimus, azathioprine and prednisolone with or without basiliximab: two-year follow-up data von Webb, Nicholas J. A., Prokurat, Sylwester, Vondrak, Karel, Watson, Alan R., Hughes, David A., Marks, Stephen D., Moghal, Nadeem E., Fitzpatrick, Maggie M., Milford, David V., Saleem, Moin A., Jones, Caroline A., Friman, Styrbjorn, Van Damme-Lombaerts, Rita, Janssen, Franςoise, Hamer, Clare, Rhodes, Sarah

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Update on congenital nephrotic syndromes and the contribution of US von Avni, E. Fred, Vandenhoute, Kate, Devriendt, Arnaud, Ismaili, Khalid, Hackx, Maxime, Janssen, Francoise, Hall, Michelle

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Antibody-Deficiency and Acute Nephritic Syndrome in a Patient with Homozygous Disruption of the CD81 Gene von van Zelm, Menno C, Smet, Julie, Mascart, Françoise, Adams, Brigitte, Schandené, Liliane, Janssen, Françoise, Ferster, Alina, van Dongen, Jacques JM, van der Burg, Mirjam

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Early prognostic factors of infants with chronic renal failure caused by renal dysplasia von ISMAILI, Khalid, SCHURMANS, Thierry, WISSING, K. Martin, HALL, Michelle, VAN AELST, Claude, JANSSEN, Francoise

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Mutations in the human laminin Delta b2 (LAMB2) gene and the associated phenotypic spectrum von Matejas, Verena, Hinkes, Bernward, Alkandari, Faisal, Al-Gazali, Lihadh, Annexstad, Ellen, Aytac, Mehmet B, Barrow, Margaret, Blahova, Kveta, Bockenhauer, Detlef, Cheong, Hae Il, Maruniak-Chudek, Iwona, Cochat, Pierre, Dotsch, Jorg, Gajjar, Priya, Hennekam, Raoul C, Janssen, Francoise, Kagan, Mikhail, Kariminejad, Ariana, Kemper, Markus J, Koenig, Jens, Kogan, Jillene, Kroes, Hester Y, Kuwertz-Broking, Eberhard, Lewanda, Amy F, Medeira, Ana, Muscheites, Jutta, Niaudet, Patrick, Pierson, Michel, Saggar, Anand, Seaver, Laurie, Suri, Mohnish, Tsygin, Alexey, Wuhl, Elke, Zurowska, Aleksandra, Uebe, Steffen, Hildebrandt, Friedhelm, Antignac, Corinne, Zenker, Martin

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