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Comment to "Recommendation on an updated standardization of serum magnesium reference ranges".
de Baaij JHF, Bockenhauer D, Claverie-Martin F, Hoenderop JGJ, Hoorn EJ, Houillier P, Knoers NVAM, Konrad M, Müller D, Nijenhuis T, Schlingmann KP, Vargas Poussou R. de Baaij JHF, et al. Among authors: houillier p. Eur J Nutr. 2022 Dec;61(8):4231-4233. doi: 10.1007/s00394-022-03004-9. Epub 2022 Sep 27. Eur J Nutr. 2022. PMID: 36168067 No abstract available.
Tissue kallikrein-deficient mice display a defect in renal tubular calcium absorption.
Picard N, Van Abel M, Campone C, Seiler M, Bloch-Faure M, Hoenderop JG, Loffing J, Meneton P, Bindels RJ, Paillard M, Alhenc-Gelas F, Houillier P. Picard N, et al. Among authors: houillier p. J Am Soc Nephrol. 2005 Dec;16(12):3602-10. doi: 10.1681/ASN.2004110923. Epub 2005 Oct 26. J Am Soc Nephrol. 2005. PMID: 16251243
TRPV5 gene polymorphisms in renal hypercalciuria.
Renkema KY, Lee K, Topala CN, Goossens M, Houillier P, Bindels RJ, Hoenderop JG. Renkema KY, et al. Among authors: houillier p. Nephrol Dial Transplant. 2009 Jun;24(6):1919-24. doi: 10.1093/ndt/gfn735. Epub 2009 Jan 8. Nephrol Dial Transplant. 2009. PMID: 19131347 Free article.
Spectrum of mutations in Gitelman syndrome.
Vargas-Poussou R, Dahan K, Kahila D, Venisse A, Riveira-Munoz E, Debaix H, Grisart B, Bridoux F, Unwin R, Moulin B, Haymann JP, Vantyghem MC, Rigothier C, Dussol B, Godin M, Nivet H, Dubourg L, Tack I, Gimenez-Roqueplo AP, Houillier P, Blanchard A, Devuyst O, Jeunemaitre X. Vargas-Poussou R, et al. Among authors: houillier p. J Am Soc Nephrol. 2011 Apr;22(4):693-703. doi: 10.1681/ASN.2010090907. Epub 2011 Mar 17. J Am Soc Nephrol. 2011. PMID: 21415153 Free PMC article.
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutations.
Godron A, Harambat J, Boccio V, Mensire A, May A, Rigothier C, Couzi L, Barrou B, Godin M, Chauveau D, Faguer S, Vallet M, Cochat P, Eckart P, Guest G, Guigonis V, Houillier P, Blanchard A, Jeunemaitre X, Vargas-Poussou R. Godron A, et al. Among authors: houillier p. Clin J Am Soc Nephrol. 2012 May;7(5):801-9. doi: 10.2215/CJN.12841211. Epub 2012 Mar 15. Clin J Am Soc Nephrol. 2012. PMID: 22422540 Free PMC article.
A pseudo-dominant form of Gitelman's syndrome.
de La Faille R, Vallet M, Venisse A, Nau V, Collet-Gaudillat C, Houillier P, Jeunemaitre X, Vargas-Poussou R. de La Faille R, et al. Among authors: houillier p. NDT Plus. 2011 Dec;4(6):386-9. doi: 10.1093/ndtplus/sfr094. Epub 2011 Aug 22. NDT Plus. 2011. PMID: 25984200 Free PMC article.
Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel Formation.
Bardet C, Courson F, Wu Y, Khaddam M, Salmon B, Ribes S, Thumfart J, Yamaguti PM, Rochefort GY, Figueres ML, Breiderhoff T, Garcia-Castaño A, Vallée B, Le Denmat D, Baroukh B, Guilbert T, Schmitt A, Massé JM, Bazin D, Lorenz G, Morawietz M, Hou J, Carvalho-Lobato P, Manzanares MC, Fricain JC, Talmud D, Demontis R, Neves F, Zenaty D, Berdal A, Kiesow A, Petzold M, Menashi S, Linglart A, Acevedo AC, Vargas-Poussou R, Müller D, Houillier P, Chaussain C. Bardet C, et al. Among authors: houillier p. J Bone Miner Res. 2016 Mar;31(3):498-513. doi: 10.1002/jbmr.2726. Epub 2015 Oct 20. J Bone Miner Res. 2016. PMID: 26426912 Free article.
Signification of distal urinary acidification defects in hypocitraturic patients.
Forni Ogna V, Blanchard A, Vargas-Poussou R, Ogna A, Baron S, Bertocchio JP, Prot-Bertoye C, Nevoux J, Dubourg J, Maruani G, Mendes M, Garcia-Castaño A, Treard C, Lepottier N, Houillier P, Courbebaisse M. Forni Ogna V, et al. Among authors: houillier p. PLoS One. 2017 May 19;12(5):e0177329. doi: 10.1371/journal.pone.0177329. eCollection 2017. PLoS One. 2017. PMID: 28542241 Free PMC article.
236 results