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Authors: JEANPIERRE C DENAMUR E HENRY I CABANIS MO LUCE S CECILLE A ELION J PEUCHMAUR M LOIRAT C NIAUDET P GUBLER MC JUNIEN C
Citation: C. Jeanpierre et al., IDENTIFICATION OF CONSTITUTIONAL WT1 MUTATIONS, IN PATIENTS WITH ISOLATED DIFFUSE MESANGIAL SCLEROSIS, AND ANALYSIS OF GENOTYPE PHENOTYPE CORRELATIONS BY USE OF A COMPUTERIZED MUTATION DATABASE/, American journal of human genetics, 62(4), 1998, pp. 824-833

Authors: NIAUDET P HABIB R
Citation: P. Niaudet et R. Habib, METHYLPREDNISOLONE PULSE THERAPY IN THE TREATMENT OF SEVERE FORMS OF SCHONLEIN-HENOCH PURPURA NEPHRITIS, Pediatric nephrology, 12(3), 1998, pp. 238-243

Authors: BERARD E SARLES J TRIOLO V GAGNADOUX MF WERNERT F HADCHOUEL M NIAUDET P
Citation: E. Berard et al., RENOVASCULAR HYPERTENSION AND VASCULAR ANOMALIES IN ALAGILLE-SYNDROME, Pediatric nephrology, 12(2), 1998, pp. 121-124

Authors: TSIMARATOS M SOTO B MOUGENOT JF BROYER M NIAUDET P
Citation: M. Tsimaratos et al., CLINICAL QUIZ - POSTANTIBIOTIC INFECTIOUS COLITIS (PSEUDOMEMBRANOUS COLITIS), Pediatric nephrology, 12(1), 1998, pp. 81-82

Authors: NIAUDET P BROYER M GUBLER MC JEANPIERRE C BARBAUX S ANTIGNAC C
Citation: P. Niaudet et al., GENETICS AND NEPHROTIC SYNDROMES, Archives de pediatrie, 5, 1998, pp. 152-155

Authors: JEANPIERRE C BEROUD C NIAUDET P JUNIEN C
Citation: C. Jeanpierre et al., SOFTWARE AND DATABASE FOR THE ANALYSIS OF MUTATIONS IN THE HUMAN WT1 GENE, Nucleic acids research, 26(1), 1998, pp. 271-274

Authors: COURTEL JV SOTO B NIAUDET P GAGNADOUX MF CARTERET M QUIGNODON JF BRUNELLE F
Citation: Jv. Courtel et al., PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY OF RENAL-ARTERY STENOSIS IN CHILDREN, Pediatric radiology, 28(1), 1998, pp. 59-63

Authors: LEMMINK HH KNOERS NVAM KAROLYI L VANDIJK H NIAUDET P ANTIGNAC C GUAYWOODFORD LM GOODYER PR CAREL JC HERMES A SEYBERTH HW MONNENS LAH VANDENHEUVEL LPWJ
Citation: Hh. Lemmink et al., NOVEL MUTATIONS IN THE THIAZIDE-SENSITIVE NACL COTRANSPORTER GENE IN PATIENTS WITH GITELMAN-SYNDROME WITH PREDOMINANT LOCALIZATION TO THE C-TERMINAL DOMAIN, Kidney international, 54(3), 1998, pp. 720-730

Authors: BROYER M CHARBIT M LEBIHAN M TETE MJ GAGNADOUX MF DROZ D GUEST G NIAUDET P
Citation: M. Broyer et al., LOSS OF GRAFT BY CHRONIC REJECTION IN A SERIES OF PEDIATRIC KIDNEY-TRANSPLANTATION - PREDICTIVE VALUE OF BIOPSY, Transplantation proceedings, 30(6), 1998, pp. 2815-2815

Authors: NIAUDET P
Citation: P. Niaudet, POSTRANSPLANT LYMPHOPROLIFERATIVE DISEASE FOLLOWING RENAL-TRANSPLANTATION - A MULTICENTER RETROSPECTIVE STUDY OF 41 CASES OBSERVED BETWEEN 1992 AND 1996, Transplantation proceedings, 30(6), 1998, pp. 2816-2817

Authors: FONTAINE E GAGNADOUX MF NIAUDET P BROYER M BEURTON D
Citation: E. Fontaine et al., RENAL-TRANSPLANTATION IN CHILDREN WITH AUGMENTATION CYSTOPLASTY - LONG-TERM RESULTS, The Journal of urology, 159(6), 1998, pp. 2110-2113

Authors: NIAUDET P
Citation: P. Niaudet, MITOCHONDRIAL DISORDERS AND THE KIDNEY, Archives of Disease in Childhood, 78(4), 1998, pp. 387-390

Authors: BARBAUX S NIAUDET P GUBLER MC GRUNFELD JP JAUBERT F KUTTENN F FEKETE CN SOULEYREAUTHERVILLE N THIBAUD E FELLOUS M MCELREAVEY K
Citation: S. Barbaux et al., DONOR SPLICE-SITE MUTATIONS IN WT1 ARE RESPONSIBLE FOR FRASIER-SYNDROME, Nature genetics, 17(4), 1997, pp. 467-470

Authors: VARGASPOUSSOU R FORESTIER L DAUTZENBERG MD NIAUDET P DECHAUX M ANTIGNAC C
Citation: R. Vargaspoussou et al., MUTATIONS IN THE VASOPRESSIN V2 RECEPTOR AND AQUAPORIN-2 GENES IN 12 FAMILIES WITH CONGENITAL NEPHROGENIC DIABETES-INSIPIDUS, Journal of the American Society of Nephrology, 8(12), 1997, pp. 1855-1862

Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPWJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC
Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY (VOL 6, PG 17, 1997), Human molecular genetics, 6(4), 1997, pp. 650-650

Authors: KAROLYI L KONRAD M KOCKERLING A ZIEGLER A ZIMMERMANN DK ROTH B WIEG C GRZESCHIK KH KOCH MC SEYBERTH HW VARGAS R FORESTIER L JEAN G DESCHAUX M RIZZONI GF NIAUDET P ANTIGNAC C FELDMANN D LORRIDON F COUGOUREUX E LAROZE F ALESSANDRI JL DAVID L SAUNIER P DESCHENES G HILDEBRANDT F VOLLMER M PROESMANS W BRANDIS M VANDENHEUVEL LPJ LEMMINK HH NILLESEN W MONNENS LAH KNOERS NVAM GUAYWOODFORD LM WRIGHT CJ MADRIGAL G HEBERT SC
Citation: L. Karolyi et al., MUTATIONS IN THE GENE ENCODING THE INWARDLY-RECTIFYING RENAL POTASSIUM CHANNEL, ROMK, CAUSE THE ANTENATAL VARIANT OF BARTTER-SYNDROME - EVIDENCE FOR GENETIC-HETEROGENEITY, Human molecular genetics, 6(1), 1997, pp. 17-26

Authors: BROYER M TERZI F LEHNERT A GAGNADOUX MF GUEST G NIAUDET P
Citation: M. Broyer et al., A CONTROLLED-STUDY OF DEFLAZACORT IN THE TREATMENT OF IDIOPATHIC NEPHROTIC SYNDROME, Pediatric nephrology, 11(4), 1997, pp. 418-422

Authors: ROTIG A LEHNERT A CHRETIEN D RUSTIN P GUBLER MC MUNNICH A NIAUDET P
Citation: A. Rotig et al., KIDNEY INVOLVEMENT IN MITOCHONDRIAL DISOR DERS, MS. Medecine sciences, 13(1), 1997, pp. 18-27

Authors: FISCHER AM TAPONBRETAUDIERE J DAUTZENBERG MD GAGNADOUX MF NIAUDET P BROYER M
Citation: Am. Fischer et al., PROPHYLACTIC ANTICOAGULANT-THERAPY IN CHILDREN UNDERGOING RENAL-TRANSPLANTATION, Thrombosis and haemostasis, 1997, pp. 1581-1581

Authors: NIAUDET P FUCHSHUBER A GAGNADOUX MF HABIB R BROYER M
Citation: P. Niaudet et al., CYCLOSPORINE IN THE THERAPY OF STEROID-RESISTANT IDIOPATHIC NEPHROTICSYNDROME, Kidney international, 1997, pp. 85-90

Authors: NIAUDET P ROTIG A
Citation: P. Niaudet et A. Rotig, THE KIDNEY IN MITOCHONDRIAL CYTOPATHIES, Kidney international, 51(4), 1997, pp. 1000-1007

Authors: LEHNERT A NIAUDET P BROYER M
Citation: A. Lehnert et al., CYTOMEGALOVIRUS-INFECTION AFTER KIDNEY-TR ANSPLANTATION IN PEDIATRIC-PATIENTS, Annales de pediatrie, 44(3), 1997, pp. 165-175

Authors: GUEST G CHARBIT M NIAUDET P GAGNADOUX MF ARSAN A POL S LACAILLE F CHAIX ML BROYER M
Citation: G. Guest et al., HEPATITIS-C INFECTION IN RENAL-TRANSPLANT RECIPIENTS - EXPERIENCE ACQUIRED AT THE ENFANTS-MALADES-TEACHING-HOSPITAL (PARIS, FRANCE), Annales de pediatrie, 44(3), 1997, pp. 183-186

Authors: FUCHSHUBER A ANTIGNAC C JEAN G GRIBOUVAL O GUBLER MC BROYER M NIAUDET P
Citation: A. Fuchshuber et al., FAMILIAL STEROID-RESISTANT NEPHROTIC SYND ROME - A NEW DISEASE ENTITYAMONG THE HEREDITARY NEPHROTIC SYNDROMES, Annales de pediatrie, 44(10), 1997, pp. 653-659

Authors: JEAN G ANTIGNAC C FUCHSHUBER A GRIBOUVAL O BROYER M NIAUDET P
Citation: G. Jean et al., CURRENT DATA ON MAPPING OF THE CYSTINOSIS GENE, Annales de pediatrie, 44(10), 1997, pp. 667-674
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