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Page 1
Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1.
Mansour-Hendili L, Blanchard A, Le Pottier N, Roncelin I, Lourdel S, Treard C, González W, Vergara-Jaque A, Morin G, Colin E, Holder-Espinasse M, Bacchetta J, Baudouin V, Benoit S, Bérard E, Bourdat-Michel G, Bouchireb K, Burtey S, Cailliez M, Cardon G, Cartery C, Champion G, Chauveau D, Cochat P, Dahan K, De la Faille R, Debray FG, Dehoux L, Deschenes G, Desport E, Devuyst O, Dieguez S, Emma F, Fischbach M, Fouque D, Fourcade J, François H, Gilbert-Dussardier B, Hannedouche T, Houillier P, Izzedine H, Janner M, Karras A, Knebelmann B, Lavocat MP, Lemoine S, Leroy V, Loirat C, Macher MA, Martin-Coignard D, Morin D, Niaudet P, Nivet H, Nobili F, Novo R, Faivre L, Rigothier C, Roussey-Kesler G, Salomon R, Schleich A, Sellier-Leclerc AL, Soulami K, Tiple A, Ulinski T, Vanhille P, Van Regemorter N, Jeunemaître X, Vargas-Poussou R. Mansour-Hendili L, et al. Among authors: desport e. Hum Mutat. 2015 Aug;36(8):743-52. doi: 10.1002/humu.22804. Epub 2015 Jun 11. Hum Mutat. 2015. PMID: 25907713 Review.
Indomethacin, amiloride, or eplerenone for treating hypokalemia in Gitelman syndrome.
Blanchard A, Vargas-Poussou R, Vallet M, Caumont-Prim A, Allard J, Desport E, Dubourg L, Monge M, Bergerot D, Baron S, Essig M, Bridoux F, Tack I, Azizi M. Blanchard A, et al. Among authors: desport e. J Am Soc Nephrol. 2015 Feb;26(2):468-75. doi: 10.1681/ASN.2014030293. Epub 2014 Jul 10. J Am Soc Nephrol. 2015. PMID: 25012174 Free PMC article. Clinical Trial.
New clinical forms of hereditary apoA-I amyloidosis entail both glomerular and retinal amyloidosis.
Colombat M, Aldigier JC, Rothschild PR, Javaugue V, Desport E, Frouget T, Goujon JM, Rioux-Leclercq N, Quellard N, Rerolle JP, Paraf F, Beugnet C, Tiple A, Durrbach A, Samuel D, Brézin A, Bridoux F, Valleix S. Colombat M, et al. Among authors: desport e. Kidney Int. 2020 Jul;98(1):195-208. doi: 10.1016/j.kint.2020.03.033. Epub 2020 Apr 23. Kidney Int. 2020. PMID: 32571483
[Current treatment of AL amyloidosis].
Desport E, Moumas E, Abraham J, Delbès S, Lacotte-Thierry L, Touchard G, Fermand JP, Bridoux F, Jaccard A. Desport E, et al. Nephrol Ther. 2011 Nov;7(6):467-73. doi: 10.1016/j.nephro.2011.02.003. Epub 2011 Apr 15. Nephrol Ther. 2011. PMID: 21497573 Review. French.
Tubulo-interstitial nephritis with Fanconi syndrome in Behçet disease.
Belmouaz S, Sechet A, Fernandez B, Ayache RA, Desport E, Bauwens M, Goujon JM, Gombert JM, Bridoux F, Touchard G. Belmouaz S, et al. Among authors: desport e. Nephrol Dial Transplant. 2007 Jul;22(7):2079-83. doi: 10.1093/ndt/gfm189. Epub 2007 Apr 3. Nephrol Dial Transplant. 2007. PMID: 17405783 No abstract available.
Acute immuno-allergic interstitial nephritis caused by fluindione.
Belmouaz S, Desport E, Abou Ayache R, Thierry A, Mignot A, Bauwens M, Goujon JM, Bridoux F, Touchard G. Belmouaz S, et al. Among authors: desport e. Clin Nephrol. 2006 Dec;66(6):455-8. doi: 10.5414/cnp66455. Clin Nephrol. 2006. PMID: 17176918
[AL amyloidosis].
Jaccard A, Desport E, Mohty D, Bridoux F. Jaccard A, et al. Among authors: desport e. Rev Med Interne. 2015 Feb;36(2):89-97. doi: 10.1016/j.revmed.2014.08.003. Epub 2014 Sep 5. Rev Med Interne. 2015. PMID: 25194219 Review. French.
39 results