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Items: 1 to 50 of 120

1.

Focal scar and diffuse myocardial fibrosis are independent imaging markers in repaired tetralogy of Fallot.

Cochet H, Iriart X, Allain-Nicolaï A, Camaioni C, Sridi S, Nivet H, Fournier E, Dinet ML, Jalal Z, Laurent F, Montaudon M, Thambo JB.

Eur Heart J Cardiovasc Imaging. 2019 Sep 1;20(9):990-1003. doi: 10.1093/ehjci/jez068.

2.

Relationship between atrial scar on cardiac magnetic resonance and pulmonary vein reconnection after catheter ablation for paroxysmal atrial fibrillation.

Jefairi NA, Camaioni C, Sridi S, Cheniti G, Takigawa M, Nivet H, Denis A, Derval N, Mathilde Merle, Laurent F, Montaudon M, Sacher F, Hocini M, Haissaguerre M, Jais P, Cochet H.

J Cardiovasc Electrophysiol. 2019 May;30(5):727-740. doi: 10.1111/jce.13908. Epub 2019 Mar 25.

PMID:
30847990
3.

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.

Pediatr Nephrol. 2018 Mar;33(3):473-483. doi: 10.1007/s00467-017-3819-9. Epub 2017 Oct 23.

PMID:
29058154
4.

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.

Hum Mutat. 2015 Aug;36(8):743-52. doi: 10.1002/humu.22804. Epub 2015 Jun 11. Review.

PMID:
25907713
5.

Age, atrial fibrillation, and structural heart disease are the main determinants of left atrial fibrosis detected by delayed-enhanced magnetic resonance imaging in a general cardiology population.

Cochet H, Mouries A, Nivet H, Sacher F, Derval N, Denis A, Merle M, Relan J, Hocini M, Haïssaguerre M, Laurent F, Montaudon M, Jaïs P.

J Cardiovasc Electrophysiol. 2015 May;26(5):484-92. doi: 10.1111/jce.12651. Epub 2015 Apr 22.

PMID:
25727248
6.

Clinical characteristics and outcomes of childhood-onset ANCA-associated vasculitis: a French nationwide study.

Sacri AS, Chambaraud T, Ranchin B, Florkin B, Sée H, Decramer S, Flodrops H, Ulinski T, Allain-Launay E, Boyer O, Dunand O, Fischbach M, Hachulla E, Pietrement C, Le Pogamp P, Stephan JL, Belot A, Nivet H, Nobili F, Guillevin L, Quartier P, Deschênes G, Salomon R, Essig M, Harambat J.

Nephrol Dial Transplant. 2015 Apr;30 Suppl 1:i104-12. doi: 10.1093/ndt/gfv011. Epub 2015 Feb 12.

PMID:
25676121
7.

Mycophenolate mofetil in patients with anti-neutrophil cytoplasmic antibody-associated vasculitis: a prospective pharmacokinetics and clinical study.

Chaigne B, Gatault P, Darrouzain F, Barbet C, Degenne D, François M, Szymanski P, Rabot N, Golea G, Diot E, Maillot F, Lebranchu Y, Nivet H, Paintaud G, Halimi JM, Guillevin L, Büchler M.

Clin Exp Immunol. 2014 May;176(2):172-9. doi: 10.1111/cei.12246.

8.

C3 nephritic factor associated with C3 glomerulopathy in children.

Nicolas C, Vuiblet V, Baudouin V, Macher MA, Vrillon I, Biebuyck-Gouge N, Dehennault M, Gié S, Morin D, Nivet H, Nobili F, Ulinski T, Ranchin B, Marinozzi MC, Ngo S, Frémeaux-Bacchi V, Pietrement C.

Pediatr Nephrol. 2014 Jan;29(1):85-94. doi: 10.1007/s00467-013-2605-6. Epub 2013 Sep 26.

PMID:
24068526
9.

Cystinosis encephalopathy: MRI perivascular enhancement with micronodular T2* hypointensity.

Cazals X, Lauvin MA, Favelle O, Domengie F, Nivet H, Cottier JP.

Diagn Interv Imaging. 2013 Jun;94(6):653-5. doi: 10.1016/j.diii.2013.03.003. Epub 2013 Apr 17. No abstract available.

10.

Kidney damage due to tuberous sclerosis complex: management recommendations.

Rouvière O, Nivet H, Grenier N, Zini L, Lechevallier E.

Diagn Interv Imaging. 2013 Mar;94(3):225-37. doi: 10.1016/j.diii.2013.01.003. Epub 2013 Feb 13.

11.

[Guidelines for the management of tuberous sclerosis complex renal disease].

Rouvière O, Nivet H, Grenier N, Zini L, Lechevallier E.

Prog Urol. 2012 Jun;22(7):367-79. doi: 10.1016/j.purol.2012.03.006. Epub 2012 Apr 30. Review. French.

PMID:
22657256
12.

Kidney transplant with multiple renal artery grafts from deceased donors: are long-term graft and patient survival compromised?

Laouad I, Bretagnol A, Fabre E, Halimi JM, Al-Najjar A, Boutin JM, Bruyère F, Nivet H, Lebranchu Y, Büchler M.

Prog Transplant. 2012 Mar;22(1):102-9.

PMID:
22489451
13.

Renal resistive index as a new independent risk factor for new-onset diabetes mellitus after kidney transplantation.

Mutinelli-Szymanski P, Caille A, Tranquart F, Al-Najjar A, Büchler M, Barbet C, Marlière JF, Gatault P, Réault J, Boin C, Chatelet V, Laouad I, Nivet H, Lebranchu Y, Halimi JM.

Transpl Int. 2012 Apr;25(4):464-70. doi: 10.1111/j.1432-2277.2012.01445.x. Epub 2012 Feb 24.

14.

An unusual case of central venous catheter-related bacteremia.

Badin J, François M, Birmelé B, Turmel-Rodrigues L, Nivet H, Pengloan J.

J Vasc Access. 2012 Jan-Mar;13(1):122-3. doi: 10.5301/JVA.5000010.

PMID:
21948129
15.

Doubling of serum creatinine in clinical trials, cost-effectiveness studies, and individual patients: adequate use in renal transplantation.

Gatault P, Al-Najjar A, Barbet C, Roland M, Laouad I, Buchler M, Marlière JF, Métais PE, Clément A, Nivet H, Lebranchu Y, Halimi JM.

Transplantation. 2011 Nov 15;92(9):1012-7. doi: 10.1097/TP.0b013e31823015e4.

PMID:
21941225
16.

Papillary stones with Randall's plaques in children: clinicobiological features and outcome.

Bouchireb K, Boyer O, Pietrement C, Nivet H, Martelli H, Dunand O, Nobili F, Sylvie GL, Niaudet P, Salomon R, Daudon M.

Nephrol Dial Transplant. 2012 Apr;27(4):1529-34. doi: 10.1093/ndt/gfr439. Epub 2011 Aug 3. No abstract available.

PMID:
21813830
17.

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.

J Am Soc Nephrol. 2011 Apr;22(4):693-703. doi: 10.1681/ASN.2010090907. Epub 2011 Mar 17.

18.

Interferon gamma licensing of human dendritic cells in T-helper-independent CD8+ alloimmunity.

Lemoine R, Velge-Roussel F, Herr F, Felix R, Nivet H, Lebranchu Y, Baron C.

Blood. 2010 Oct 21;116(16):3089-98. doi: 10.1182/blood-2010-02-268623. Epub 2010 Jul 19.

19.

Autosomal dominant polycystic kidney disease: risk factor for nonmelanoma skin cancer following kidney transplantation.

Bretagnol A, Halimi JM, Roland M, Barbet C, Machet L, Al Najjar A, Marlière JF, Badin J, Nivet H, Lebranchu Y, Büchler M.

Transpl Int. 2010 Sep;23(9):878-86. doi: 10.1111/j.1432-2277.2010.01070.x. Epub 2010 Mar 5.

20.

Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome.

Harambat J, Fargue S, Acquaviva C, Gagnadoux MF, Janssen F, Liutkus A, Mourani C, Macher MA, Abramowicz D, Legendre C, Durrbach A, Tsimaratos M, Nivet H, Girardin E, Schott AM, Rolland MO, Cochat P.

Kidney Int. 2010 Mar;77(5):443-9. doi: 10.1038/ki.2009.435. Epub 2009 Dec 16.

21.

Hydatid cyst disease in a renal allograft recipient.

Sqalli TH, Buchler M, Al Najjar A, Paris A, Halimi JM, Nivet H, Anthonioz P, Bourlier P, Duong TH, Lebranchu Y.

Saudi J Kidney Dis Transpl. 2009 Nov;20(6):1057-60. No abstract available.

22.

Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1.

Fargue S, Harambat J, Gagnadoux MF, Tsimaratos M, Janssen F, Llanas B, Berthélémé JP, Boudailliez B, Champion G, Guyot C, Macher MA, Nivet H, Ranchin B, Salomon R, Taque S, Rolland MO, Cochat P.

Kidney Int. 2009 Oct;76(7):767-73. doi: 10.1038/ki.2009.237. Epub 2009 Jul 1.

23.

Mycophenolate mofetil in patients with systemic lupus erythematosus: a prospective pharmacokinetic study.

Roland M, Barbet C, Paintaud G, Magdelaine-Beuzelin C, Diot E, Halimi JM, Lebranchu Y, Nivet H, Büchler M.

Lupus. 2009 Apr;18(5):441-7. doi: 10.1177/0961203308098631.

PMID:
19318398
24.

[Clinical variability and diagnosis steps in childhood mitochondrial disease].

Mercier S, Josselin de Wasch M, Labarthe F, Jardel C, Lombès A, Munnich A, Toutain A, Nivet H, Saliba E, Chantepie A, Castelnau P.

Arch Pediatr. 2009 Apr;16(4):322-30. doi: 10.1016/j.arcped.2008.12.024. Epub 2009 Feb 23. French.

PMID:
19233626
25.

Mutations of NPHP2 and NPHP3 in infantile nephronophthisis.

Tory K, Rousset-Rouvière C, Gubler MC, Morinière V, Pawtowski A, Becker C, Guyot C, Gié S, Frishberg Y, Nivet H, Deschênes G, Cochat P, Gagnadoux MF, Saunier S, Antignac C, Salomon R.

Kidney Int. 2009 Apr;75(8):839-47. doi: 10.1038/ki.2008.662. Epub 2009 Jan 28.

26.

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome.

Frémeaux-Bacchi V, Miller EC, Liszewski MK, Strain L, Blouin J, Brown AL, Moghal N, Kaplan BS, Weiss RA, Lhotta K, Kapur G, Mattoo T, Nivet H, Wong W, Gie S, Hurault de Ligny B, Fischbach M, Gupta R, Hauhart R, Meunier V, Loirat C, Dragon-Durey MA, Fridman WH, Janssen BJ, Goodship TH, Atkinson JP.

Blood. 2008 Dec 15;112(13):4948-52. doi: 10.1182/blood-2008-01-133702. Epub 2008 Sep 16.

27.

An antenatal hyper-echogenic colon: question.

Merieau E, Cloarec S, Benoist JF, Haddad G, Benoit S, Nivet H.

Pediatr Nephrol. 2009 Feb;24(2):275, 277-9. doi: 10.1007/s00467-008-0930-y. Epub 2008 Aug 13. No abstract available.

PMID:
18704508
28.

Early pulse pressure and low-grade proteinuria as independent long-term risk factors for new-onset diabetes mellitus after kidney transplantation.

Roland M, Gatault P, Al-Najjar A, Doute C, Barbet C, Chatelet V, Laouad I, Marlière JF, Nivet H, Büchler M, Lebranchu Y, Halimi JM.

Am J Transplant. 2008 Aug;8(8):1719-28. doi: 10.1111/j.1600-6143.2008.02308.x.

29.

Induction of human CD4+ regulatory T cells by mycophenolic acid-treated dendritic cells.

Lagaraine C, Lemoine R, Baron C, Nivet H, Velge-Roussel F, Lebranchu Y.

J Leukoc Biol. 2008 Oct;84(4):1057-64. doi: 10.1189/jlb.1007716. Epub 2008 Jul 8.

PMID:
18611986
30.

Rituximab treatment for severe steroid- or cyclosporine-dependent nephrotic syndrome: a multicentric series of 22 cases.

Guigonis V, Dallocchio A, Baudouin V, Dehennault M, Hachon-Le Camus C, Afanetti M, Groothoff J, Llanas B, Niaudet P, Nivet H, Raynaud N, Taque S, Ronco P, Bouissou F.

Pediatr Nephrol. 2008 Aug;23(8):1269-79. doi: 10.1007/s00467-008-0814-1. Epub 2008 May 9.

PMID:
18465150
31.

Immunosuppressive medications, clinical and metabolic parameters in new-onset diabetes mellitus after kidney transplantation.

Roland M, Gatault P, Doute C, Büchler M, Al-Najjar A, Barbet C, Chatelet V, Marlière JF, Nivet H, Lebranchu Y, Halimi JM.

Transpl Int. 2008 Jun;21(6):523-30. doi: 10.1111/j.1432-2277.2008.00640.x. Epub 2008 Feb 4.

32.

[Renal transplantation in patients with autosomal dominant polycystic kidney disease: pre-transplantation evaluation and follow-up].

Bretagnol A, Büchler M, Boutin JM, Nivet H, Lebranchu Y, Chauveau D.

Nephrol Ther. 2007 Dec;3(7):449-55. Epub 2007 Sep 4. Review. French.

PMID:
18047999
33.

Respective predictive role of urinary albumin excretion and nonalbumin proteinuria on graft loss and death in renal transplant recipients.

Halimi JM, Matthias B, Al-Najjar A, Laouad I, Chatelet V, Marlière JF, Nivet H, Lebranchu Y.

Am J Transplant. 2007 Dec;7(12):2775-81. Epub 2007 Oct 19.

34.

Disappearance of tophi in familial juvenile hyperuricemic nephropathy after kidney transplantation.

Merieau E, Al Najjar A, Halimi JM, Sacquépée M, Nivet H, Lebranchu Y, Büchler M.

Am J Transplant. 2007 Nov;7(11):2634-6. Epub 2007 Sep 14.

35.

Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome.

Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA, Macher MA, Niaudet P, Guest G, Boudailliez B, Bouissou F, Deschenes G, Gie S, Tsimaratos M, Fischbach M, Morin D, Nivet H, Alberti C, Loirat C; French Society of Pediatric Nephrology.

J Am Soc Nephrol. 2007 Aug;18(8):2392-400. Epub 2007 Jun 28.

36.

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.

Delous M, Baala L, Salomon R, Laclef C, Vierkotten J, Tory K, Golzio C, Lacoste T, Besse L, Ozilou C, Moutkine I, Hellman NE, Anselme I, Silbermann F, Vesque C, Gerhardt C, Rattenberry E, Wolf MT, Gubler MC, Martinovic J, Encha-Razavi F, Boddaert N, Gonzales M, Macher MA, Nivet H, Champion G, Berthélémé JP, Niaudet P, McDonald F, Hildebrandt F, Johnson CA, Vekemans M, Antignac C, Rüther U, Schneider-Maunoury S, Attié-Bitach T, Saunier S.

Nat Genet. 2007 Jul;39(7):875-81. Epub 2007 Jun 10.

PMID:
17558409
37.

High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations.

Tory K, Lacoste T, Burglen L, Morinière V, Boddaert N, Macher MA, Llanas B, Nivet H, Bensman A, Niaudet P, Antignac C, Salomon R, Saunier S.

J Am Soc Nephrol. 2007 May;18(5):1566-75. Epub 2007 Apr 4.

38.

[Urinary infections in the child and the adult. Leukocyturia ].

Barbet C, Nivet H.

Rev Prat. 2006 Nov 30;56(18):2073-8; quiz 2078. Review. French. No abstract available.

PMID:
17274516
39.

Urinary albumin excretion and the risk of graft loss and death in proteinuric and non-proteinuric renal transplant recipients.

Halimi JM, Buchler M, Al-Najjar A, Laouad I, Chatelet V, Marlière JF, Nivet H, Lebranchu Y.

Am J Transplant. 2007 Mar;7(3):618-25. Epub 2007 Jan 11.

40.

Early proteinuria is a strong indicator of donor renal lesions, ischemia-reperfusion injury and immunological aggression.

Halimi J, Laouad I, Buchler M, Al-Najjar A, Chatelet V, Houssaini TS, Nivet H, Lebranchu Y.

Transplant Proc. 2006 Sep;38(7):2319-20.

PMID:
16980078
41.

Estimation of the glomerular filtration rate through different methods in kidney transplant recipients: correlation with the creatinine clearance measurement.

Büchler M, Bretagnol A, Desaldeleer C, Garreau P, Halimi JM, Al-Najjar A, Marlière JF, Nivet H, Lebranchu Y.

Transplant Proc. 2006 Sep;38(7):2289-91.

PMID:
16980067
42.

Genetic investigation of autosomal recessive distal renal tubular acidosis: evidence for early sensorineural hearing loss associated with mutations in the ATP6V0A4 gene.

Vargas-Poussou R, Houillier P, Le Pottier N, Strompf L, Loirat C, Baudouin V, Macher MA, Déchaux M, Ulinski T, Nobili F, Eckart P, Novo R, Cailliez M, Salomon R, Nivet H, Cochat P, Tack I, Fargeot A, Bouissou F, Kesler GR, Lorotte S, Godefroid N, Layet V, Morin G, Jeunemaître X, Blanchard A.

J Am Soc Nephrol. 2006 May;17(5):1437-43. Epub 2006 Apr 12.

43.

Recurrence of nephrotic syndrome after renal transplantation: influence of increased immunosuppression.

Nathanson S, Cochat P, André JL, Guyot C, Loirat C, Nivet H, Deschênes G.

Pediatr Nephrol. 2005 Dec;20(12):1801-4. Epub 2005 Oct 14.

PMID:
16228184
44.

Recipient age and mycophenolate mofetil as the main determinants of outcome after steroid withdrawal: analysis of long-term follow-up in renal transplantation.

Laouad I, Halimi JM, Büchler M, Al-Najjar A, Chatelet V, Nivet H, Lebranchu Y.

Transplantation. 2005 Sep 27;80(6):872-4.

PMID:
16210979
45.

Early low-grade proteinuria: causes, short-term evolution and long-term consequences in renal transplantation.

Halimi JM, Laouad I, Buchler M, Al-Najjar A, Chatelet V, Houssaini TS, Nivet H, Lebranchu Y.

Am J Transplant. 2005 Sep;5(9):2281-8.

46.

Occupational exposure in ANCA-positive patients: a case-control study.

Beaudreuil S, Lasfargues G, Lauériere L, El Ghoul Z, Fourquet F, Longuet C, Halimi JM, Nivet H, Büchler M.

Kidney Int. 2005 May;67(5):1961-6.

47.

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome.

Dragon-Durey MA, Loirat C, Cloarec S, Macher MA, Blouin J, Nivet H, Weiss L, Fridman WH, Frémeaux-Bacchi V.

J Am Soc Nephrol. 2005 Feb;16(2):555-63. Epub 2004 Dec 8.

48.

Living with a functioning kidney transplant at 74 yr or older: a national epidemiological study.

Büchler M, Halimi JM, Najjar AA, Giral M, Hiesse C, Giraudeau B, Jacquelinet C, Nivet H, Lebranchu Y.

Clin Transplant. 2004 Dec;18(6):681-5.

PMID:
15516244
49.

Death after withdrawal from dialysis: the most common cause of death in a French dialysis population.

Birmelé B, François M, Pengloan J, Français P, Testou D, Brillet G, Lechapois D, Baudin S, Grezard O, Jourdan JL, Fodil-Cherif M, Abaza M, Dupouet L, Fournier G, Nivet H.

Nephrol Dial Transplant. 2004 Mar;19(3):686-91.

PMID:
14767027
50.

[Demography of nephrologists in France in 2002].

Nivet H, Maingourd C, Mignon F.

Nephrologie. 2003;24(8):431-6. French.

PMID:
14737975

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