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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1979 4
1980 2
1981 3
1982 2
1984 1
1985 1
1986 2
1987 2
1988 2
1989 2
1990 2
1991 3
1993 1
1994 7
1995 5
1996 9
1997 2
1999 2
2000 3
2001 3
2002 5
2003 6
2004 4
2005 5
2006 4
2007 7
2008 6
2009 7
2010 3
2011 3
2012 5
2013 3
2014 2
2015 3
2017 1
2018 1
2019 2
2020 4
2021 4
2022 1
2024 1
2025 0

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129 results

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Page 1
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: nivet h. 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.
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: nivet h. Hum Mutat. 2015 Aug;36(8):743-52. doi: 10.1002/humu.22804. Epub 2015 Jun 11. Hum Mutat. 2015. PMID: 25907713 Review.
[Can man live with a pig kidney?].
Valentin JF, Lebranchu Y, Nivet H. Valentin JF, et al. Among authors: nivet h. Nephrologie. 1999;20(4):189-92. Nephrologie. 1999. PMID: 10480150 Review. French.
Cyclosporin-induced muscular toxicity.
Grezard O, Lebranchu Y, Birmele B, Sharobeem R, Nivet H, Bagros P. Grezard O, et al. Among authors: nivet h. Lancet. 1990 Jan 20;335(8682):177. doi: 10.1016/0140-6736(90)90057-c. Lancet. 1990. PMID: 1967475 No abstract available.
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome.
Dorval G, Gribouval O, Martinez-Barquero V, Machuca E, Tête MJ, Baudouin V, Benoit S, Chabchoub I, Champion G, Chauveau D, Chehade H, Chouchane C, Cloarec S, Cochat P, Dahan K, Dantal J, Delmas Y, Deschênes G, Dolhem P, Durand D, Ekinci Z, El Karoui K, Fischbach M, Grunfeld JP, Guigonis V, Hachicha M, Hogan J, Hourmant M, Hummel A, Kamar N, Krummel T, Lacombe D, Llanas B, Mesnard L, Mohsin N, Niaudet P, Nivet H, Parvex P, Pietrement C, de Pontual L, Noble CP, Ribes D, Ronco P, Rondeau E, Sallee M, Tsimaratos M, Ulinski T, Salomon R, Antignac C, Boyer O. Dorval G, et al. Among authors: nivet h. Pediatr Nephrol. 2018 Mar;33(3):473-483. doi: 10.1007/s00467-017-3819-9. Epub 2017 Oct 23. Pediatr Nephrol. 2018. PMID: 29058154
The accuracy of teleradiologists in diagnosing COVID-19 based on a French multicentric emergency cohort.
Nivet H, Crombé A, Schuster P, Ayoub T, Pourriol L, Favard N, Chazot A, Alonzo-Lacroix F, Youssof E, Ben Cheikh A, Balique J, Porta B, Petitpierre F, Bouquet G, Mastier C, Bratan F, Bergerot JF, Thomson V, Banaste N, Gorincour G. Nivet H, et al. Eur Radiol. 2021 May;31(5):2833-2844. doi: 10.1007/s00330-020-07345-z. Epub 2020 Oct 29. Eur Radiol. 2021. PMID: 33123790 Free PMC article.
129 results