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Items: 1 to 50 of 165

1.

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.

2.

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.

3.

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.

4.

Darbepoetin, effective treatment of anaemia in paediatric patients with chronic renal failure.

André JL, Deschênes G, Boudailliez B, Broux F, Fischbach M, Gagnadoux MF, Horen B, Lahoche-Manucci A, Macher MA, Roussel B, Tsimaratos M, Loirat C.

Pediatr Nephrol. 2007 May;22(5):708-14. Epub 2007 Jan 11.

PMID:
17216497
5.

Prognosis of autosomal dominant polycystic kidney disease diagnosed in utero or at birth.

Boyer O, Gagnadoux MF, Guest G, Biebuyck N, Charbit M, Salomon R, Niaudet P.

Pediatr Nephrol. 2007 Mar;22(3):380-8. Epub 2006 Nov 24.

PMID:
17124604
6.

Cyclosporin therapy in patients with Alport syndrome.

Charbit M, Gubler MC, Dechaux M, Gagnadoux MF, Grünfeld JP, Niaudet P.

Pediatr Nephrol. 2007 Jan;22(1):57-63. Epub 2006 Sep 21.

PMID:
17024394
7.

Body growth after combined liver-kidney transplantation in children with primary hyperoxaluria type 1.

Nissel R, Latta K, Gagnadoux MF, Kelly D, Hulton S, Kemper MJ, Ruder H, Söderdahl G, Otte JB, Cochat P, Roquet O, Jamieson NV, Haffner D.

Transplantation. 2006 Jul 15;82(1):48-54.

PMID:
16861941
8.

Respiratory chain deficiency presenting as congenital nephrotic syndrome.

Goldenberg A, Ngoc LH, Thouret MC, Cormier-Daire V, Gagnadoux MF, Chrétien D, Lefrançois C, Geromel V, Rötig A, Rustin P, Munnich A, Paquis V, Antignac C, Gubler MC, Niaudet P, de Lonlay P, Bérard E.

Pediatr Nephrol. 2005 Apr;20(4):465-9. Epub 2005 Jan 29.

PMID:
15682315
9.

Long-term social outcome of children after kidney transplantation.

Broyer M, Le Bihan C, Charbit M, Guest G, Tete MJ, Gagnadoux MF, Niaudet P.

Transplantation. 2004 Apr 15;77(7):1033-7.

PMID:
15087767
10.

A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulin.

Dahan K, Devuyst O, Smaers M, Vertommen D, Loute G, Poux JM, Viron B, Jacquot C, Gagnadoux MF, Chauveau D, Büchler M, Cochat P, Cosyns JP, Mougenot B, Rider MH, Antignac C, Verellen-Dumoulin C, Pirson Y.

J Am Soc Nephrol. 2003 Nov;14(11):2883-93.

11.

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.

Otto EA, Schermer B, Obara T, O'Toole JF, Hiller KS, Mueller AM, Ruf RG, Hoefele J, Beekmann F, Landau D, Foreman JW, Goodship JA, Strachan T, Kispert A, Wolf MT, Gagnadoux MF, Nivet H, Antignac C, Walz G, Drummond IA, Benzing T, Hildebrandt F.

Nat Genet. 2003 Aug;34(4):413-20.

12.

Cystine crystal volume determination: a useful tool in the management of cystinuric patients.

Daudon M, Cohen-Solal F, Barbey F, Gagnadoux MF, Knebelmann B, Jungers P.

Urol Res. 2003 Jul;31(3):207-11. Epub 2003 May 14.

PMID:
12748836
13.

Intravenous cyclosporine therapy in recurrent nephrotic syndrome after renal transplantation in children.

Salomon R, Gagnadoux MF, Niaudet P.

Transplantation. 2003 Mar 27;75(6):810-4.

PMID:
12660507
14.

Steroid-sensitive nephrotic syndrome: from childhood to adulthood.

Fakhouri F, Bocquet N, Taupin P, Presne C, Gagnadoux MF, Landais P, Lesavre P, Chauveau D, Knebelmann B, Broyer M, Grünfeld JP, Niaudet P.

Am J Kidney Dis. 2003 Mar;41(3):550-7.

PMID:
12612977
15.

Prenatal diagnosis of bilateral isolated fetal hyperechogenic kidneys. Is it possible to predict long term outcome?

Tsatsaris V, Gagnadoux MF, Aubry MC, Gubler MC, Dumez Y, Dommergues M.

BJOG. 2002 Dec;109(12):1388-93.

17.

High serum levels of a non-(1-84) parathyroid hormone (PTH) fragment in pediatric haemodialysis patients.

Salomon R, Charbit M, Gagnadoux MF, Niaudet P, Gao P, Cantor T, Souberbielle JC.

Pediatr Nephrol. 2001 Dec;16(12):1011-4.

PMID:
11793090
18.

Long term results of liver-kidney transplantation in children with primary hyperoxaluria.

Gagnadoux MF, Lacaille F, Niaudet P, Revillon Y, Jouvet P, Jan D, Guest G, Charbit M, Broyer M.

Pediatr Nephrol. 2001 Dec;16(12):946-50.

PMID:
11793078
19.

Urological complications after renal transplantation using ureteroureteral anastomosis in children.

Lapointe SP, Charbit M, Jan D, Lortat-Jacob S, Michel JL, Beurton D, Gagnadoux MF, Niaudet P, Broyer M, Révillon Y.

J Urol. 2001 Sep;166(3):1046-8.

PMID:
11490295
20.

Autosomal recessive polycystic kidney disease in adulthood.

Fonck C, Chauveau D, Gagnadoux MF, Pirson Y, Grünfeld JP.

Nephrol Dial Transplant. 2001 Aug;16(8):1648-52.

PMID:
11477168
21.

[Socioprofessional future in adulthood of children with end-stage kidney failure].

Broyer M, Charbit M, Guest G, Gagnadoux MF.

Arch Pediatr. 2001 May;8 Suppl 2:215s-217s. French. No abstract available.

PMID:
11394066
22.

[Cystine lithiasis: physiopathology and medical treatment].

Jungers P, Joly D, Gagnadoux MF, Daudon M.

Prog Urol. 2001 Feb;11(1):122-6. Review. French. No abstract available.

PMID:
11296632
23.

Hemolytic-uremic syndrome: hereditary forms and forms associated with hereditary diseases.

Niaudet P, Gagnadoux MF, Broyer M, Salomon R.

Adv Nephrol Necker Hosp. 2000;30:261-80. Review. No abstract available.

PMID:
11068647
24.

[Prenatal diagnosis of autosomal recessive polycystic kidney disease].

Gagnadoux MF, Attié T, Amiel J, Gigarel N, Bonnefont JP, Munnich A, Gubler MC, Antignac C.

Arch Pediatr. 2000 Sep;7(9):942-7. French.

PMID:
11028201
25.

Alterations of protein metabolism by metabolic acidosis in children with chronic renal failure.

Boirie Y, Broyer M, Gagnadoux MF, Niaudet P, Bresson JL.

Kidney Int. 2000 Jul;58(1):236-41.

26.

Pretransplant blood transfusions with cyclosporine in pediatric renal transplantation.

Niaudet P, Dudley J, Charbit M, Gagnadoux MF, Macleay K, Broyer M.

Pediatr Nephrol. 2000 Jun;14(6):451-6.

PMID:
10872182
27.

Role of the bladder in delayed failure of kidney transplants in boys with posterior urethral valves.

Salomon L, Fontaine E, Guest G, Gagnadoux MF, Broyer M, Beurton D.

J Urol. 2000 Apr;163(4):1282-5.

PMID:
10737529
28.

Treatment of cystinuria.

Joly D, Rieu P, Méjean A, Gagnadoux MF, Daudon M, Jungers P.

Pediatr Nephrol. 1999 Nov;13(9):945-50. Review.

PMID:
10603157
29.

Chronic renal failure after Puumala virus infection.

Novo R, Gagnadoux MF, Le Guenno Y, Gubler MC, Niaudet P, Guyot C, Broyer M.

Pediatr Nephrol. 1999 Nov;13(9):934-5.

PMID:
10603154
30.

Diabetes mellitus in patients with infantile cystinosis after renal transplantation.

Robert JJ, Tête MJ, Guest G, Gagnadoux MF, Niaudet P, Broyer M.

Pediatr Nephrol. 1999 Aug;13(6):524-9.

PMID:
10452283
31.

Human herpes virus-8 and other risk factors for Kaposi's sarcoma in kidney transplant recipients. Groupe Cooperatif de Transplantation d' Ile de France (GCIF).

Farge D, Lebbé C, Marjanovic Z, Tuppin P, Mouquet C, Peraldi MN, Lang P, Hiesse C, Antoine C, Legendre C, Bedrossian J, Gagnadoux MF, Loirat C, Pellet C, Sheldon J, Golmard JL, Agbalika F, Schulz TF.

Transplantation. 1999 May 15;67(9):1236-42.

PMID:
10342315
32.

Risk of primary disease recurrence in pediatric renal transplantation.

Gagnadoux MF, Niaudet P, Droz D, Gubler MC, Broyer M.

Transplant Proc. 1999 Feb-Mar;31(1-2):235. No abstract available.

PMID:
10083089
33.

Treatment of childhood steroid-resistant idiopathic nephrotic syndrome.

Niaudet P, Gagnadoux MF, Broyer M.

Adv Nephrol Necker Hosp. 1998;28:43-61. Review. No abstract available.

PMID:
9889985
34.

Loss of graft by chronic rejection in a series of pediatric kidney transplantation: predictive value of biopsy.

Broyer M, Charbit M, Lebihan M, Tete MJ, Gagnadoux MF, Droz D, Guest G, Niaudet P.

Transplant Proc. 1998 Sep;30(6):2815. No abstract available.

PMID:
9745578
35.

Renal transplantation in children with augmentation cystoplasty: long-term results.

Fontaine E, Gagnadoux MF, Niaudet P, Broyer M, Beurton D.

J Urol. 1998 Jun;159(6):2110-3.

PMID:
9598551
36.

Crystalluria: a clinically useful investigation in children with primary hyperoxaluria post-transplantation.

Jouvet P, Priqueler L, Gagnadoux MF, Jan D, Beringer A, Lacaille F, Revillon Y, Broyer M, Daudon M.

Kidney Int. 1998 May;53(5):1412-6.

37.

Renovascular hypertension and vascular anomalies in Alagille syndrome.

Bérard E, Sarles J, Triolo V, Gagnadoux MF, Wernert F, Hadchouel M, Niaudet P.

Pediatr Nephrol. 1998 Feb;12(2):121-4.

PMID:
9543369
38.

Percutaneous transluminal angioplasty of renal artery stenosis in children.

Courtel JV, Soto B, Niaudet P, Gagnadoux MF, Carteret M, Quignodon JF, Brunelle F.

Pediatr Radiol. 1998 Jan;28(1):59-63. Review.

PMID:
9426277
39.

The diagnosis of the cystic lesion and the causal relationship between the cyst and the hematuria.

Gagnadoux MF.

Pediatr Nephrol. 1998 Jan;12(1):86. No abstract available.

PMID:
9502579
40.

[Cystic kidney diseases].

Gagnadoux MF.

Rev Prat. 1997 Sep 15;47(14):1536-40. French.

PMID:
9366110
41.

Vascular access for hemodialysis in children.

Bourquelot P, Gagnadoux MF.

Pediatr Nephrol. 1997 Oct;11(5):659-60. No abstract available.

PMID:
9323303
42.

Long-term results of renal transplantation in children with the prune-belly syndrome.

Fontaine E, Salomon L, Gagnadoux MF, Niaudet P, Broyer M, Beurton D.

J Urol. 1997 Sep;158(3 Pt 1):892-4.

PMID:
9258114
43.

Pregnancy in renal transplantation: a pediatric unit report.

Arsan A, Guest G, Gagnadoux MF, Broyer M.

Transplant Proc. 1997 Aug;29(5):2479. No abstract available.

PMID:
9270818
44.

A controlled study of deflazacort in the treatment of idiopathic nephrotic syndrome.

Broyer M, Terzi F, Lehnert A, Gagnadoux MF, Guest G, Niaudet P.

Pediatr Nephrol. 1997 Aug;11(4):418-22.

PMID:
9260237
45.

Posterior urethral valves: long-term renal function consequences after transplantation.

Salomon L, Fontaine E, Gagnadoux MF, Broyer M, Beurton D.

J Urol. 1997 Mar;157(3):992-5.

PMID:
9072633
46.

Cyclosporine in the therapy of steroid-resistant idiopathic nephrotic syndrome.

Niaudet P, Fuchshuber A, Gagnadoux MF, Habib R, Broyer M.

Kidney Int Suppl. 1997 Mar;58:S85-90. Review.

PMID:
9067953
47.

Varicella and zoster in children after kidney transplantation: long-term results of vaccination.

Broyer M, Tete MJ, Guest G, Gagnadoux MF, Rouzioux C.

Pediatrics. 1997 Jan;99(1):35-9.

PMID:
8989334
48.

Oligomeganephronic renal hypoplasia.

Broyer M, Soto B, Gagnadoux MF, Adi M, Rica C, Gubler MC.

Adv Nephrol Necker Hosp. 1997;26:47-63. No abstract available.

PMID:
8922124
49.

Renal function in young patients on long-term cyclic parenteral nutrition.

Colomb V, Charbit M, Goulet O, de Potter S, Corriol O, Gagnadoux MF, Dechaux M, Ricour C.

Transplant Proc. 1996 Oct;28(5):2785. No abstract available.

PMID:
8908059
50.

Long-term (15-25 years) outcome of childhood hemolytic-uremic syndrome.

Gagnadoux MF, Habib R, Gubler MC, Bacri JL, Broyer M.

Clin Nephrol. 1996 Jul;46(1):39-41.

PMID:
8832149

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