Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 30

1.

Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function.

Bedin M, Boyer O, Servais A, Li Y, Villoing-Gaudé L, Tête MJ, Cambier A, Hogan J, Baudouin V, Krid S, Bensman A, Lammens F, Louillet F, Ranchin B, Vigneau C, Bouteau I, Isnard-Bagnis C, Mache CJ, Schäfer T, Pape L, Gödel M, Huber TB, Benz M, Klaus G, Hansen M, Latta K, Gribouval O, Morinière V, Tournant C, Grohmann M, Kuhn E, Wagner T, Bole-Feysot C, Jabot-Hanin F, Nitschké P, Ahluwalia TS, Köttgen A, Andersen CBF, Bergmann C, Antignac C, Simons M.

J Clin Invest. 2020 Jan 2;130(1):335-344. doi: 10.1172/JCI129937.

2.

Identification of genetic causes for sporadic steroid-resistant nephrotic syndrome in adults.

Gribouval O, Boyer O, Hummel A, Dantal J, Martinez F, Sberro-Soussan R, Etienne I, Chauveau D, Delahousse M, Lionet A, Allard J, Pouteil Noble C, Tête MJ, Heidet L, Antignac C, Servais A.

Kidney Int. 2018 Nov;94(5):1013-1022. doi: 10.1016/j.kint.2018.07.024.

PMID:
30348286
3.

APOL1 risk genotype in European steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis patients of different African ancestries.

Gribouval O, Boyer O, Knebelmann B, Karras A, Dantal J, Fourrage C, Alibeu O, Hogan J, Dossier C, Tête MJ, Antignac C, Servais A.

Nephrol Dial Transplant. 2019 Nov 1;34(11):1885-1893. doi: 10.1093/ndt/gfy176.

PMID:
29992269
4.

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
5.

LMX1B mutations cause hereditary FSGS without extrarenal involvement.

Boyer O, Woerner S, Yang F, Oakeley EJ, Linghu B, Gribouval O, Tête MJ, Duca JS, Klickstein L, Damask AJ, Szustakowski JD, Heibel F, Matignon M, Baudouin V, Chantrel F, Champigneulle J, Martin L, Nitschké P, Gubler MC, Johnson KJ, Chibout SD, Antignac C.

J Am Soc Nephrol. 2013 Jul;24(8):1216-22. doi: 10.1681/ASN.2013020171. Epub 2013 May 16.

6.

INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy.

Boyer O, Nevo F, Plaisier E, Funalot B, Gribouval O, Benoit G, Huynh Cong E, Arrondel C, Tête MJ, Montjean R, Richard L, Karras A, Pouteil-Noble C, Balafrej L, Bonnardeaux A, Canaud G, Charasse C, Dantal J, Deschenes G, Deteix P, Dubourg O, Petiot P, Pouthier D, Leguern E, Guiochon-Mantel A, Broutin I, Gubler MC, Saunier S, Ronco P, Vallat JM, Alonso MA, Antignac C, Mollet G.

N Engl J Med. 2011 Dec 22;365(25):2377-88. doi: 10.1056/NEJMoa1109122.

7.

Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults.

Brodin-Sartorius A, Tête MJ, Niaudet P, Antignac C, Guest G, Ottolenghi C, Charbit M, Moyse D, Legendre C, Lesavre P, Cochat P, Servais A.

Kidney Int. 2012 Jan;81(2):179-89. doi: 10.1038/ki.2011.277. Epub 2011 Sep 7.

8.

Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis.

Boyer O, Benoit G, Gribouval O, Nevo F, Tête MJ, Dantal J, Gilbert-Dussardier B, Touchard G, Karras A, Presne C, Grunfeld JP, Legendre C, Joly D, Rieu P, Mohsin N, Hannedouche T, Moal V, Gubler MC, Broutin I, Mollet G, Antignac C.

J Am Soc Nephrol. 2011 Feb;22(2):239-45. doi: 10.1681/ASN.2010050518. Epub 2011 Jan 21.

9.

Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome.

Machuca E, Benoit G, Nevo F, Tête MJ, Gribouval O, Pawtowski A, Brandström P, Loirat C, Niaudet P, Gubler MC, Antignac C.

J Am Soc Nephrol. 2010 Jul;21(7):1209-17. doi: 10.1681/ASN.2009121309. Epub 2010 May 27.

10.

Nephrin mutations can cause childhood-onset steroid-resistant nephrotic syndrome.

Philippe A, Nevo F, Esquivel EL, Reklaityte D, Gribouval O, Tête MJ, Loirat C, Dantal J, Fischbach M, Pouteil-Noble C, Decramer S, Hoehne M, Benzing T, Charbit M, Niaudet P, Antignac C.

J Am Soc Nephrol. 2008 Oct;19(10):1871-8. doi: 10.1681/ASN.2008010059. Epub 2008 Jul 9.

11.

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

Weber S, Gribouval O, Esquivel EL, Morinière V, Tête MJ, Legendre C, Niaudet P, Antignac C.

Kidney Int. 2004 Aug;66(2):571-9.

12.

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
13.

Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy.

Castelnau P, Le Merrer M, Diatloff-Zito C, Marquis E, Tête MJ, Robert JJ.

Eur J Pediatr. 2000 Aug;159(8):631-3.

PMID:
10968248
14.

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
15.

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
16.

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
17.

Clinical polymorphism of cystinosis encephalopathy. Results of treatment with cysteamine.

Broyer M, Tête MJ, Guest G, Berthélémé JP, Labrousse F, Poisson M.

J Inherit Metab Dis. 1996;19(1):65-75.

PMID:
8830179
18.

[Long-term results of kidney grafts in children. Apropos of a series of 332 grafts performed prior to 1984].

Broyer M, Tete MJ, Guest G, Arsan A, Gagnadoux MF, Habib R, Beurton D.

Arch Pediatr. 1996;3 Suppl 1:135s-137s. French. No abstract available.

PMID:
8795993
19.

[Sugar diabetes after renal transplantation in children].

Robert JJ, Tete MJ, Crosnier H, Broyer M.

Ann Pediatr (Paris). 1993 Feb;40(2):112-8. Review. French.

PMID:
8457131
20.

[Urinary lithiasis after kidney transplantation. Experience at a pediatric center].

Guest G, Tete MJ, Beurton D, Broyer M.

Arch Fr Pediatr. 1993 Jan;50(1):15-9. French.

PMID:
8507133
21.

[Intra-leukocyte cystine in cystinosis treated with cysteamine].

Ged C, Jean G, Tete MJ, Broyer M, Kamoun P.

Ann Biol Clin (Paris). 1991;49(9):482-6. French.

PMID:
1789502
22.

[Treatment of cystinosis using cysteamine].

Broyer M, Tete MJ.

Ann Pediatr (Paris). 1990 Feb;37(2):91-3. French.

PMID:
2321906
23.

Cyclosporine and childhood idiopathic nephrosis.

Niaudet P, Tete MJ, Broyer M, Habib R.

Transplant Proc. 1988 Jun;20(3 Suppl 4):265-8. No abstract available.

PMID:
3381281
24.

Treatment of severe childhood nephrosis.

Niaudet P, Habib R, Gagnadoux MF, Tete MJ, Broyer M.

Adv Nephrol Necker Hosp. 1988;17:151-72. No abstract available.

PMID:
3124538
25.

Cyclosporin in the treatment of idiopathic nephrotic syndrome in children.

Niaudet P, Habib R, Tete MJ, Hinglais N, Broyer M.

Pediatr Nephrol. 1987 Oct;1(4):566-73.

PMID:
3153333
26.

Late symptoms in infantile cystinosis.

Broyer M, Tete MJ, Gubler MC.

Pediatr Nephrol. 1987 Jul;1(3):519-24.

PMID:
3153326
27.

[Pharmacokinetics of prednisone after oral administration in children with renal grafts. Changes induced by phenobarbital and renal insufficiency].

Perignon F, Pecquinot MA, Ged C, Antignac C, Guest G, Tete MJ, Broyer M, Lenoir G.

Arch Fr Pediatr. 1985 Aug-Sep;42 Suppl 1:639-44. French.

PMID:
3909980
28.

Plasma lipids, lipoproteins and apolipoproteins AI, AII, and B in renal transplanted children: what risk for accelerated atherosclerosis?

Goldstein S, Duhamel G, Laudat MH, Berthelier M, Hervy C, Tete MJ, Broyer M.

Nephron. 1984;38(2):87-92.

PMID:
6433214
29.
30.

Insulin and growth hormone secretion in dialyzed children: influence of dietary manipulation.

Broyer M, Czernichow P, Tete MJ, Laudat MH, Dartois AM.

Am J Clin Nutr. 1978 Oct;31(10):1876-90.

PMID:
707342

Supplemental Content

Support Center