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Items: 26

1.

School level of children carrying a HNF1B variant or a deletion.

Laliève F, Decramer S, Heidet L, Baudouin V, Lahoche A, Llanas B, Cochat P, Tenenbaum J, Lavocat MP, Eckart P, Broux F, Roussey G, Cloarec S, Vrillon I, Dunand O, Bessenay L, Tsimaratos M, Nobili F, Pietrement C, De Parscau L, Bonneville V, Rodier N, Saint-Martin C, Chassaing N, Michel-Calemard L, Moriniere V, Bellanné-Chantelot C, Bahans C, Guigonis V.

Eur J Hum Genet. 2020 Jan;28(1):56-63. doi: 10.1038/s41431-019-0490-6. Epub 2019 Sep 3.

PMID:
31481685
2.

Social deprivation is associated with poor kidney transplantation outcome in children.

Driollet B, Bayer F, Chatelet V, Macher MA, Salomon R, Ranchin B, Roussey G, Lahoche A, Garaix F, Decramer S, Mérieau E, Fila M, Zaloszyc A, Deschênes G, Valeri L, Launay L, Couchoud C, Leffondré K, Harambat J.

Kidney Int. 2019 Sep;96(3):769-776. doi: 10.1016/j.kint.2019.05.011. Epub 2019 May 28.

PMID:
31375259
3.

Quality of life in adolescents with chronic kidney disease who initiate haemodialysis treatment.

Clavé S, Tsimaratos M, Boucekine M, Ranchin B, Salomon R, Dunand O, Garnier A, Lahoche A, Fila M, Roussey G, Broux F, Harambat J, Cloarec S, Menouer S, Deschenes G, Vrillon I, Auquier P, Berbis J.

BMC Nephrol. 2019 May 14;20(1):163. doi: 10.1186/s12882-019-1365-3.

4.

Complement Gene Variants and Shiga Toxin-Producing Escherichia coli-Associated Hemolytic Uremic Syndrome: Retrospective Genetic and Clinical Study.

Frémeaux-Bacchi V, Sellier-Leclerc AL, Vieira-Martins P, Limou S, Kwon T, Lahoche A, Novo R, Llanas B, Nobili F, Roussey G, Cailliez M, Ulinski T, Deschênes G, Alberti C, Weill FX, Mariani P, Loirat C.

Clin J Am Soc Nephrol. 2019 Mar 7;14(3):364-377. doi: 10.2215/CJN.05830518. Epub 2019 Jan 23.

PMID:
30674459
5.

Interactions between perceived exertion and thermal perception in the heat in endurance athletes.

Roussey G, Gruet M, Vercruyssen F, Louis J, Vallier JM, Bernard T.

J Therm Biol. 2018 Aug;76:68-76. doi: 10.1016/j.jtherbio.2018.07.006. Epub 2018 Jul 11.

PMID:
30143299
6.

Patient and transplant outcome in infants starting renal replacement therapy before 2 years of age.

Hogan J, Bacchetta J, Charbit M, Roussey G, Novo R, Tsimaratos M, Terzic J, Ulinski T, Garnier A, Merieau E, Harambat J, Vrillon I, Dunand O, Morin D, Berard E, Nobili F, Couchoud C, Macher MA; French Pediatric Nephrology Society.

Nephrol Dial Transplant. 2018 Aug 1;33(8):1459-1465. doi: 10.1093/ndt/gfy040.

PMID:
29617835
7.

Ofatumumab in post-transplantation recurrence of a pediatric steroid-resistant idiopathic nephrotic syndrome.

Bernard J, Bruel A, Allain-Launay E, Dantal J, Roussey G.

Pediatr Transplant. 2018 Jun;22(4):e13175. doi: 10.1111/petr.13175. Epub 2018 Mar 23.

PMID:
29569812
8.

Treatment and outcome of congenital nephrotic syndrome.

Bérody S, Heidet L, Gribouval O, Harambat J, Niaudet P, Baudouin V, Bacchetta J, Boudaillez B, Dehennault M, de Parscau L, Dunand O, Flodrops H, Fila M, Garnier A, Louillet F, Macher MA, May A, Merieau E, Monceaux F, Pietrement C, Rousset-Rouvière C, Roussey G, Taque S, Tenenbaum J, Ulinski T, Vieux R, Zaloszyc A, Morinière V, Salomon R, Boyer O.

Nephrol Dial Transplant. 2019 Mar 1;34(3):458-467. doi: 10.1093/ndt/gfy015.

PMID:
29474669
9.

Treatment by immunoadsorption for recurrent focal segmental glomerulosclerosis after paediatric kidney transplantation: a multicentre French cohort.

Allard L, Kwon T, Krid S, Bacchetta J, Garnier A, Novo R, Deschenes G, Salomon R, Roussey G, Allain-Launay E.

Nephrol Dial Transplant. 2018 Jun 1;33(6):954-963. doi: 10.1093/ndt/gfx214.

PMID:
28992235
10.

Effect of center practices on the choice of the first dialysis modality for children and young adults.

Hogan J, Ranchin B, Fila M, Harambat J, Krid S, Vrillon I, Roussey G, Fischbach M, Couchoud C.

Pediatr Nephrol. 2017 Apr;32(4):659-667. doi: 10.1007/s00467-016-3538-7. Epub 2016 Nov 14.

PMID:
27844146
11.

Stability and Compatibility of Antibiotics in Peritoneal Dialysis Solutions Applied to Automated Peritoneal Dialysis in The Pediatric Population.

Deslandes G, Grégoire M, Bouquié R, Le Marec A, Allard S, Dailly E, Pineau A, Allain-Launay E, Jolliet P, Roussey G, Navas D.

Perit Dial Int. 2016 11-12;36(6):676-679. Epub 2016 May 4.

12.

Calcineurin Inhibitors Downregulate HNF-1β and May Affect the Outcome of HNF1B Patients After Renal Transplantation.

Faguer S, Esposito L, Casemayou A, Pirson Y, Decramer S, Cartery C, Hazzan M, Garrigue V, Roussey G, Cointault O, Ho T, Merville P, Devuyst O, Gourdy P, Chassaing N, Bascands JL, Kamar N, Schanstra JP, Rostaing L, Chauveau D.

Transplantation. 2016 Sep;100(9):1970-8. doi: 10.1097/TP.0000000000000993.

13.

A case of hypercalcemia Indications for 1,25-dihydroxyvitamin D prescription.

Malandain D, Roussey G, Leloupp AG, Graveline N, Masson D, Bach-Ngohou K.

Ann Biol Clin (Paris). 2015 Sep-Oct;73(5):573-80. doi: 10.1684/abc.2015.1071.

14.

Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease.

Audrézet MP, Corbiere C, Lebbah S, Morinière V, Broux F, Louillet F, Fischbach M, Zaloszyc A, Cloarec S, Merieau E, Baudouin V, Deschênes G, Roussey G, Maestri S, Visconti C, Boyer O, Abel C, Lahoche A, Randrianaivo H, Bessenay L, Mekahli D, Ouertani I, Decramer S, Ryckenwaert A, Cornec-Le Gall E, Salomon R, Ferec C, Heidet L.

J Am Soc Nephrol. 2016 Mar;27(3):722-9. doi: 10.1681/ASN.2014101051. Epub 2015 Jul 2.

15.

Characterization and review of MTHFD1 deficiency: four new patients, cellular delineation and response to folic and folinic acid treatment.

Burda P, Kuster A, Hjalmarson O, Suormala T, Bürer C, Lutz S, Roussey G, Christa L, Asin-Cayuela J, Kollberg G, Andersson BA, Watkins D, Rosenblatt DS, Fowler B, Holme E, Froese DS, Baumgartner MR.

J Inherit Metab Dis. 2015 Sep;38(5):863-72. doi: 10.1007/s10545-015-9810-3. Epub 2015 Jan 30. Review.

PMID:
25633902
16.

Regional citrate anticoagulation for pediatric CRRT using integrated citrate software.

Liet JM, Roussey G.

Pediatr Nephrol. 2014 Sep;29(9):1647. doi: 10.1007/s00467-014-2881-9. Epub 2014 Aug 7. No abstract available.

PMID:
25099081
17.

Failure of bortezomib to cure acute antibody-mediated rejection in a non-compliant renal transplant patient.

Ryckewaert A, Allain-Launay E, Moreau A, Blancho G, Cesbron A, Blin N, Roussey G.

Pediatr Transplant. 2013 Sep;17(6):E131-6. doi: 10.1111/petr.12113. Epub 2013 Jul 9.

PMID:
23834525
18.

Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.

Jaureguiberry G, De la Dure-Molla M, Parry D, Quentric M, Himmerkus N, Koike T, Poulter J, Klootwijk E, Robinette SL, Howie AJ, Patel V, Figueres ML, Stanescu HC, Issler N, Nicholson JK, Bockenhauer D, Laing C, Walsh SB, McCredie DA, Povey S, Asselin A, Picard A, Coulomb A, Medlar AJ, Bailleul-Forestier I, Verloes A, Le Caignec C, Roussey G, Guiol J, Isidor B, Logan C, Shore R, Johnson C, Inglehearn C, Al-Bahlani S, Schmittbuhl M, Clauss F, Huckert M, Laugel V, Ginglinger E, Pajarola S, Spartà G, Bartholdi D, Rauch A, Addor MC, Yamaguti PM, Safatle HP, Acevedo AC, Martelli-Júnior H, dos Santos Netos PE, Coletta RD, Gruessel S, Sandmann C, Ruehmann D, Langman CB, Scheinman SJ, Ozdemir-Ozenen D, Hart TC, Hart PS, Neugebauer U, Schlatter E, Houillier P, Gahl WA, Vikkula M, Bloch-Zupan A, Bleich M, Kitagawa H, Unwin RJ, Mighell A, Berdal A, Kleta R.

Nephron Physiol. 2012;122(1-2):1-6. doi: 10.1159/000349989. Epub 2013 Feb 23.

19.

Renal phenotypic variability in HDR syndrome: glomerular nephropathy as a novel finding.

Chenouard A, Isidor B, Allain-Launay E, Moreau A, Le Bideau M, Roussey G.

Eur J Pediatr. 2013 Jan;172(1):107-10. doi: 10.1007/s00431-012-1845-y. Epub 2012 Oct 5.

PMID:
23052618
20.

The natural history of clinical operational tolerance after kidney transplantation through twenty-seven cases.

Brouard S, Pallier A, Renaudin K, Foucher Y, Danger R, Devys A, Cesbron A, Guillot-Guegen C, Ashton-Chess J, Le Roux S, Harb J, Roussey G, Subra JF, Villemain F, Legendre C, Bemelman FJ, Orlando G, Garnier A, Jambon H, Le Monies De Sagazan H, Braun L, Noël C, Pillebout E, Moal MC, Cantarell C, Hoitsma A, Ranbant M, Testa A, Soulillou JP, Giral M.

Am J Transplant. 2012 Dec;12(12):3296-307. doi: 10.1111/j.1600-6143.2012.04249.x. Epub 2012 Sep 13.

21.

Kidney and liver transplantation in patients with autosomal recessive polycystic kidney disease: a multicentric study.

Chapal M, Debout A, Dufay A, Salomon R, Roussey G, Burtey S, Launay EA, Vigneau C, Blancho G, Loirat C, Hourmant M, Fakhouri F.

Nephrol Dial Transplant. 2012 May;27(5):2083-8. doi: 10.1093/ndt/gfr588. Epub 2011 Nov 9.

PMID:
22076432
22.

Population pharmacokinetics and pharmacogenetics of mycophenolic acid following administration of mycophenolate mofetil in de novo pediatric renal-transplant patients.

Zhao W, Fakhoury M, Deschênes G, Roussey G, Brochard K, Niaudet P, Tsimaratos M, André JL, Cloarec S, Cochat P, Bensman A, Azougagh S, Jacqz-Aigrain E.

J Clin Pharmacol. 2010 Nov;50(11):1280-91. doi: 10.1177/0091270009357429. Epub 2010 Feb 10.

PMID:
20147615
23.

Population pharmacokinetics and pharmacogenetics of tacrolimus in de novo pediatric kidney transplant recipients.

Zhao W, Elie V, Roussey G, Brochard K, Niaudet P, Leroy V, Loirat C, Cochat P, Cloarec S, André JL, Garaix F, Bensman A, Fakhoury M, Jacqz-Aigrain E.

Clin Pharmacol Ther. 2009 Dec;86(6):609-18. doi: 10.1038/clpt.2009.210. Epub 2009 Oct 28.

PMID:
19865079
24.

Dominant tolerance to kidney allografts induced by anti-donor MHC class II antibodies: cooperation between T and non-T CD103+ cells.

Degauque N, Lair D, Dupont A, Moreau A, Roussey G, Moizant F, Hubert FX, Louvet C, Hill M, Haspot F, Josien R, Usal C, Vanhove B, Soulillou JP, Brouard S.

J Immunol. 2006 Apr 1;176(7):3915-22.

25.

[Value of multidetector-row computed tomography for infantile renovascular hypertension: report of two cases].

Isnard J, Launay-Gillard S, Roussey G, Quere MP.

J Radiol. 2006 Feb;87(2 Pt 1):143-5. French.

PMID:
16484939
26.

Recherche d'une substance cancérigène dans le foie de rat soumis à l'action du benxopyrène.

ROUSSEY G, GUERIN M.

C R Seances Soc Biol Fil. 1947 Feb;141(3-4):93. Undetermined Language. No abstract available.

PMID:
20268948

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