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Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies. [electronic resource] by
- Debiec, Hanna
- Nauta, Jeroen
- Coulet, Florence
- van der Burg, Mirjam
- Guigonis, Vincent
- Schurmans, Thierry
- de Heer, Emile
- Soubrier, Florent
- Janssen, Francoise
- Ronco, Pierre
Producer: 20041015
In:
Lancet (London, England) vol. 364
Availability: No items available.
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Clinical characteristics and outcomes of children with stage 3-5 chronic kidney disease. [electronic resource] by
- 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
Producer: 20100618
In:
Pediatric nephrology (Berlin, Germany) vol. 25
Availability: No items available.
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CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency. [electronic resource] by
- 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
Producer: 20100421
In:
The Journal of clinical investigation vol. 120
Availability: No items available.
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Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome. [electronic resource] by
- 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
Producer: 20100519
In:
Kidney international vol. 77
Availability: No items available.
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Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1. [electronic resource] by
- 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
Producer: 20091230
In:
Kidney international vol. 76
Availability: No items available.
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Multicentre prospective randomised trial of tacrolimus, azathioprine and prednisolone with or without basiliximab: two-year follow-up data. [electronic resource] by
- 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, Francoise
- Hamer, Clare
- Rhodes, Sarah
Producer: 20090416
In:
Pediatric nephrology (Berlin, Germany) vol. 24
Availability: No items available.
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Mutations in the human laminin beta2 (LAMB2) gene and the associated phenotypic spectrum. [electronic resource] by
- Matejas, Verena
- Hinkes, Bernward
- Alkandari, Faisal
- Al-Gazali, Lihadh
- Annexstad, Ellen
- Aytac, Mehmet B
- Barrow, Margaret
- Bláhová, Kveta
- 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
Producer: 20101208
In:
Human mutation vol. 31
Availability: No items available.
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