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Results: 1-25 | 26-50 | 51-75 | 76-82
Results: 1-25/82
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/
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
DIFFUSE LEIOMYOMATOSIS OF THE ESOPHAGUS - DISORDER OF CELL-MATRIX INTERACTION
Authors: THORNER P HEIDET L MERLO FM EDWARDS V ANTIGNAC C GUBLER MC
Citation: P. Thorner et al., DIFFUSE LEIOMYOMATOSIS OF THE ESOPHAGUS - DISORDER OF CELL-MATRIX INTERACTION, PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 1(6), 1998, pp. 543-549
FAMILIAL JUVENILE NEPHRONOPHTHISIS
Authors: KONRAD M SAUNIER S CALADO J GUBLER MC BROYER M ANTIGNAC C
Citation: M. Konrad et al., FAMILIAL JUVENILE NEPHRONOPHTHISIS, Journal of molecular medicine, 76(5), 1998, pp. 310-316
CHRONOLOGY OF RENAL SCARRING IN MALES WITH ALPORT-SYNDROME
Authors: KASHTAN CE GUBLER MC SISSONROSS S MAUER M
Citation: Ce. Kashtan et al., CHRONOLOGY OF RENAL SCARRING IN MALES WITH ALPORT-SYNDROME, Pediatric nephrology, 12(4), 1998, pp. 269-274
GENETICS AND NEPHROTIC SYNDROMES
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
TARGETS OF ALLOANTIBODIES IN ALPORT ANTIGLOMERULAR BASEMENT-MEMBRANE DISEASE AFTER RENAL-TRANSPLANTATION
Authors: BRAINWOOD D KASHTAN C GUBLER MC TURNER AN
Citation: D. Brainwood et al., TARGETS OF ALLOANTIBODIES IN ALPORT ANTIGLOMERULAR BASEMENT-MEMBRANE DISEASE AFTER RENAL-TRANSPLANTATION, Kidney international, 53(3), 1998, pp. 762-766
SOMATIC DELETION OF THE 5'-END OF BOTH THE COL4A5 AND COL4A6 GENES INA SPORADIC LEIOMYOMA OF THE ESOPHAGUS
Authors: HEIDET L BOYE E CAI Y SADO Y ZHANG X FLEJOU JF FEKETE F NINOMIYA Y GUBLER MC ANTIGNAC C
Citation: L. Heidet et al., SOMATIC DELETION OF THE 5'-END OF BOTH THE COL4A5 AND COL4A6 GENES INA SPORADIC LEIOMYOMA OF THE ESOPHAGUS, The American journal of pathology, 152(3), 1998, pp. 673-678
DETERMINATION OF THE GENOMIC STRUCTURE OF THE COL4A4 GENE AND OF NOVEL MUTATIONS CAUSING AUTOSOMAL RECESSIVE ALPORT-SYNDROME
Authors: BOYE E MOLLET G FORESTIER L COHENSOLAL L HEIDET H COCHAT P GRUNFELD JP PALCOUX JB GUBLER MC ANTIGNAC C
Citation: E. Boye et al., DETERMINATION OF THE GENOMIC STRUCTURE OF THE COL4A4 GENE AND OF NOVEL MUTATIONS CAUSING AUTOSOMAL RECESSIVE ALPORT-SYNDROME, American journal of human genetics, 63(5), 1998, pp. 1329-1340
DONOR SPLICE-SITE MUTATIONS IN WT1 ARE RESPONSIBLE FOR FRASIER-SYNDROME
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
CLINICAL AND PATHOPHYSIOLOGICAL ASPECTS OF IMMUNE-COMPLEX GLOMERULONEPHRITIS ASSOCIATED WITH ENTAMOEBA-HISTOLYTICA ABSCESS OF THE LIVER
Authors: LECUIT M MARTINEZ F DERAY G BEAUFILS H GUBLER MC NOZAIS JP BRICAIRE F JACOBS C
Citation: M. Lecuit et al., CLINICAL AND PATHOPHYSIOLOGICAL ASPECTS OF IMMUNE-COMPLEX GLOMERULONEPHRITIS ASSOCIATED WITH ENTAMOEBA-HISTOLYTICA ABSCESS OF THE LIVER, Clinical infectious diseases, 25(2), 1997, pp. 335-336
PROLIFERATION AND APOPTOSIS IN DENYS-DRASH-SYNDROME AND ISOLATED DIFFUSE MESANGIAL SCLEROSIS
Authors: YANG YX GUBLER MC
Citation: Yx. Yang et Mc. Gubler, PROLIFERATION AND APOPTOSIS IN DENYS-DRASH-SYNDROME AND ISOLATED DIFFUSE MESANGIAL SCLEROSIS, Journal of the American Society of Nephrology, 8, 1997, pp. 1998-1998
EXPRESSION OF WT1 AND PAX-2 IN IDIOPATHIC COLLAPSING GLOMERULOPATHY (ICG) AND HIV-ASSOCIATED NEPHROPATHY (HIV-AN)
Authors: YANG YX BEAUFILS H GUBLER MC
Citation: Yx. Yang et al., EXPRESSION OF WT1 AND PAX-2 IN IDIOPATHIC COLLAPSING GLOMERULOPATHY (ICG) AND HIV-ASSOCIATED NEPHROPATHY (HIV-AN), Journal of the American Society of Nephrology, 8, 1997, pp. 2544-2544
A NOVEL GENE THAT ENCODES A PROTEIN WITH A PUTATIVE SRC HOMOLOGY-3 DOMAIN IS A CANDIDATE GENE FOR FAMILIAL JUVENILE NEPHRONOPHTHISIS
Authors: SAUNIER S CALADO J HEILIG R SILBERMANN F BENESSY F MORIN G KONRAD M BROYER M GUBLER MC WEISSENBACH J ANTIGNAC C
Citation: S. Saunier et al., A NOVEL GENE THAT ENCODES A PROTEIN WITH A PUTATIVE SRC HOMOLOGY-3 DOMAIN IS A CANDIDATE GENE FOR FAMILIAL JUVENILE NEPHRONOPHTHISIS, Human molecular genetics, 6(13), 1997, pp. 2317-2323
CHRONIC-RENAL-FAILURE AND CRANIOECTODERMAL DYSPLASIA - A FURTHER STEP
Authors: TSIMARATOS M BERARD E SIGAUDY S ALMAHANA T DELARUE A ROQUELAURE B COSTET C ANTIGNAC C GUBLER MC PICON G PHILIP N SARLES J
Citation: M. Tsimaratos et al., CHRONIC-RENAL-FAILURE AND CRANIOECTODERMAL DYSPLASIA - A FURTHER STEP, Pediatric nephrology, 11(6), 1997, pp. 785-786
DISTRIBUTION OF ALPHA-INTEGRIN SUBUNITS IN FETAL POLYCYSTIC KIDNEY-DISEASES
Authors: DAIKHADAHMANE F NARCY F DOMMERGUES M LACOSTE M BEZIAU A GUBLER MC
Citation: F. Daikhadahmane et al., DISTRIBUTION OF ALPHA-INTEGRIN SUBUNITS IN FETAL POLYCYSTIC KIDNEY-DISEASES, Pediatric nephrology, 11(3), 1997, pp. 267-273
KIDNEY INVOLVEMENT IN MITOCHONDRIAL DISOR DERS
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
ALPORTS-SYNDROME - HEREDITARY MUTATIONS I N THE TYPE-IV COLLAGEN FAMILY
Authors: HEIDET L FORESTIER L ANTIGNAC C GUBLER MC
Citation: L. Heidet et al., ALPORTS-SYNDROME - HEREDITARY MUTATIONS I N THE TYPE-IV COLLAGEN FAMILY, MS. Medecine sciences, 13(1), 1997, pp. 28-36
NOVEL COL4A5 COL4A6 DELETIONS AND FURTHER CHARACTERIZATION OF THE DIFFUSE LEIOMYOMATOSIS-ALPORT-SYNDROME (DL-AS) LOCUS DEFINE THE DL CRITICAL REGION/
Authors: HEIDET L COHENSOLAL L BOYE E THORNER P KEMPER MJ DAVID A PIET LL ZHOU J FLINTER F ZHANG X GUBLER MC ANTIGNAC C
Citation: L. Heidet et al., NOVEL COL4A5 COL4A6 DELETIONS AND FURTHER CHARACTERIZATION OF THE DIFFUSE LEIOMYOMATOSIS-ALPORT-SYNDROME (DL-AS) LOCUS DEFINE THE DL CRITICAL REGION/, Cytogenetics and cell genetics, 78(3-4), 1997, pp. 240-246
MALFORMATIONS AND DISEASES OF THE FETAL KIDNEY
Authors: GUBLER MC DAHMANE F DOMMERGUES M NARCY F
Citation: Mc. Gubler et al., MALFORMATIONS AND DISEASES OF THE FETAL KIDNEY, Annales de pathologie, 17(4), 1997, pp. 240-250
DEVELOPMENT OF HUMAN FETAL KIDNEY IN OBSTRUCTIVE UROPATHY - CORRELATIONS WITH ULTRASONOGRAPHY AND URINE BIOCHEMISTRY
Authors: DAIKHADAHMANE F DOMMERGUES M MULLER F NARCY F LACOSTE M BEZIAU A DUMEZ Y GUBLER MC
Citation: F. Daikhadahmane et al., DEVELOPMENT OF HUMAN FETAL KIDNEY IN OBSTRUCTIVE UROPATHY - CORRELATIONS WITH ULTRASONOGRAPHY AND URINE BIOCHEMISTRY, Kidney international, 52(1), 1997, pp. 21-32
FAMILIAL STEROID-RESISTANT NEPHROTIC SYND ROME - A NEW DISEASE ENTITYAMONG THE HEREDITARY NEPHROTIC SYNDROMES
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
DEVELOPMENT OF THE KIDNEY - RECENT MOLECU LAR-BIOLOGY DATA
Authors: GUBLER MC
Citation: Mc. Gubler, DEVELOPMENT OF THE KIDNEY - RECENT MOLECU LAR-BIOLOGY DATA, Annales de pediatrie, 44(10), 1997, pp. 692-700
RENAL-FAILURE FROM MITOCHONDRIAL CYTOPATHIES
Authors: BUEMI M ALLEGRA A ROTIG A GUBLER MC ALOISI C CORICA F PETTINATO G FRISINA N NIAUDET P
Citation: M. Buemi et al., RENAL-FAILURE FROM MITOCHONDRIAL CYTOPATHIES, Nephron, 76(3), 1997, pp. 249-253
DIFFUSE LEIOMYOMATOSIS ASSOCIATED WITH X-LINKED ALPORT SYNDROME - EXTRACELLULAR-MATRIX STUDY USING IMMUNOHISTOCHEMISTRY AND IN-SITU HYBRIDIZATION
Authors: HEIDET L CAI Y SADO Y NINOMIYA Y THORNER P GUICHARNAUD L BOYE E CHAUVET V SOLAL LC BEZIAU A TORRES RG ANTIGNAC C GUBLER MC
Citation: L. Heidet et al., DIFFUSE LEIOMYOMATOSIS ASSOCIATED WITH X-LINKED ALPORT SYNDROME - EXTRACELLULAR-MATRIX STUDY USING IMMUNOHISTOCHEMISTRY AND IN-SITU HYBRIDIZATION, Laboratory investigation, 76(2), 1997, pp. 233-243
SOMATIC DELETION OF THE 5'-ENDS OF BOTH THE COL4A5 AND COL4A6 GENES IN A SPORADIC LEIOMYOMA OR THE ESOPHAGUS
Authors: HEIDEL L BOYE E CAI Y SADO Y NINOMIYA Y GUBLER MC ANTIGNAC C
Citation: L. Heidel et al., SOMATIC DELETION OF THE 5'-ENDS OF BOTH THE COL4A5 AND COL4A6 GENES IN A SPORADIC LEIOMYOMA OR THE ESOPHAGUS, American journal of human genetics, 61(4), 1997, pp. 368-368
Risultati: 1-25 | 26-50 | 51-75 | 76-82