AAAAAA
Results: 1-25/34
Authors:
de Lonlay, P
Valnot, I
Barrientos, A
Gorbatyuk, M
Tzagoloff, A
Taanman, JW
Benayoun, E
Chretien, D
Kadhom, N
Lombes, A
de Baulny, HO
Niaudet, P
Munnich, M
Rustin, P
Rotig, A
Citation: P. De Lonlay et al., A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure, NAT GENET, 29(1), 2001, pp. 57-60
Authors:
Sahali, D
Pawlak, A
Le Gouvello, S
Lang, P
Valanciute, A
Remy, P
Loirat, C
Niaudet, P
Bensman, A
Guellaen, G
Citation: D. Sahali et al., Transcriptional and post-transcriptional alterations of I kappa B alpha inactive minimal-change nephrotic syndrome, J AM S NEPH, 12(8), 2001, pp. 1648-1658
Authors:
Niaudet, P
Reigneau, O
Humbert, H
Citation: P. Niaudet et al., A pharmacokinetic study of Neoral in childhood steroid-dependent nephroticsyndrome, PED NEPHROL, 16(2), 2001, pp. 154-155
Authors:
Niaudet, P
Citation: P. Niaudet, Congenital nephrotic syndrome: commentary, PED NEPHROL, 16(2), 2001, pp. 190-191
Authors:
Pietrement, C
Salomon, R
Monceaux, F
Petitjean, C
Niaudet, P
Citation: C. Pietrement et al., Analgesia by oxygen-nitrous oxide mixture during percutaneous renal biopsyin children., ARCH PED, 8(2), 2001, pp. 145-149
Authors:
Niaudet, P
Antignac, C
Citation: P. Niaudet et C. Antignac, News on nephrotic syndrome, ARCH PED, 8, 2001, pp. 311S-313S
Authors:
Salomon, R
Tellier, AL
Attie-Bitach, T
Amiel, J
Vekemans, M
Lyonnet, S
Dureau, P
Niaudet, P
Gubler, MC
Broyer, M
Citation: R. Salomon et al., PAX2 mutations in oligomeganephronia, KIDNEY INT, 59(2), 2001, pp. 457-462
Authors:
Lapointe, SP
Charbit, M
Jan, D
Lortat-Jacob, S
Michel, JL
Beurton, D
Gagnadoux, MF
Niaudet, P
Broyer, M
Revillon, Y
Citation: Sp. Lapointe et al., Urological complications after renal transplantation using ureteroureteralanastomosis in children, J UROL, 166(3), 2001, pp. 1046-1048
Authors:
Boute, N
Gribouval, O
Roselli, S
Benessy, F
Lee, H
Fuchshuber, A
Dahan, K
Gubler, MC
Niaudet, P
Antignac, C
Citation: N. Boute et al., NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome, NAT GENET, 24(4), 2000, pp. 349-354
Authors:
Salomon, R
Gubler, MC
Niaudet, P
Citation: R. Salomon et al., Genetics of the nephrotic syndrome, CURR OP PED, 12(2), 2000, pp. 129-134
Authors:
Niaudet, P
Broyer, M
Citation: P. Niaudet et M. Broyer, Management of steroid-responsive nephrotic syndrome, PED NEPHROL, 14(8-9), 2000, pp. 770-771
Authors:
Niaudet, P
Dudley, J
Charbit, M
Gagnadoux, MF
Macleay, K
Broyer, M
Citation: P. Niaudet et al., Pretransplant blood transfusions with cyclosporine in pediatric renal transplantation, PED NEPHROL, 14(6), 2000, pp. 451-456
Authors:
Denamur, E
Andre, JL
Niaudet, P
Loirat, C
Citation: E. Denamur et al., Absence of correlation between genotype and the severity of diffuse mesangial sclerosis in Denys-Drash syndrome, PED NEPHROL, 14(5), 2000, pp. 439-440
Authors:
Niaudet, P
Citation: P. Niaudet, Treatment of lupus nephritis in children, PED NEPHROL, 14(2), 2000, pp. 158-166
Authors:
Niaudet, P
Citation: P. Niaudet, Nephrotic syndrome following hepatitis B vaccination, PED NEPHROL, 14(1), 2000, pp. 91-91
Authors:
Boirie, Y
Broyer, M
Gagnadoux, MF
Niaudet, P
Bresson, JL
Citation: Y. Boirie et al., Alterations of protein metabolism by metabolic acidosis in children with chronic renal failure, KIDNEY INT, 58(1), 2000, pp. 236-241
Authors:
Denamur, E
Bocquet, N
Baudouin, V
Da Silva, F
Veitia, R
Peuchmaur, M
Elion, J
Gubler, MC
Fellous, M
Niaudet, P
Loirat, C
Citation: E. Denamur et al., WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis, KIDNEY INT, 57(5), 2000, pp. 1868-1872
Authors:
Sterkers, G
Baudouin, V
Ansart-Pirenne, H
Maisin, A
Niaudet, P
Cochat, P
Loirat, C
Citation: G. Sterkers et al., Duration of action of a chimeric interleukin-2 receptor monoclonal antibody, basiliximab, in pediatric kidney transplant recipients, TRANSPLAN P, 32(8), 2000, pp. 2757-2759
Authors:
Aggoun, Y
Niaudet, P
Laffont, A
Sidi, D
Kachaner, J
Bonnet, D
Citation: Y. Aggoun et al., Arterial and cardiac assessment of end stage renal disease in children on hemodialysis., ARCH MAL C, 93(8), 2000, pp. 1009-1013
Authors:
Barbosa, AS
Hadjiathanasiou, CG
Theodoridis, C
Papathanasiou, A
Tar, A
Merksz, M
Gyorvari, B
Sultan, C
Dumas, R
Jaubert, F
Niaudet, P
Moreira, CA
Cotinot, C
Fellous, M
Citation: As. Barbosa et al., The same mutation affecting the splicing of WT1 gene is present on Frasiersyndrome patients with or without Wilms' tumor, HUM MUTAT, 13(2), 1999, pp. 146-153
Authors:
Novo, R
Gagnadoux, MF
Le Guenno, Y
Gubler, MC
Niaudet, P
Guyot, C
Broyer, M
Citation: R. Novo et al., Chronic renal failure after Puumala virus infection, PED NEPHROL, 13(9), 1999, pp. 934-935
Authors:
Robert, JJ
Tete, MJ
Guest, G
Gagnadoux, MF
Niaudet, P
Broyer, M
Citation: Jj. Robert et al., Diabetes mellitus in patients with infantile cystinosis after renal transplantation, PED NEPHROL, 13(6), 1999, pp. 524-529
Authors:
Niaudet, P
Citation: P. Niaudet, Management of lupus nephritis in children., ARCH PED, 6(12), 1999, pp. 1312-1321
Authors:
Labrune, P
Zittoun, J
Duvaltier, I
Trioche, P
Niaudet, P
Odievre, M
Citation: P. Labrune et al., Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiency, EUR J PED, 158(9), 1999, pp. 734-739
Authors:
Coutant, R
Leroy, B
Niaudet, P
Loirat, C
Dommergues, JP
Andre, JL
Baculard, A
Bensman, A
Citation: R. Coutant et al., Renal Granulomatous sarcoidosis in childhood: a report of 11 cases and a review of the literature, EUR J PED, 158(2), 1999, pp. 154-159