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Results: 1-15 |
Results: 15
Molecular analysis of uromodulin and SAH genes, positional candidates for autosomal dominant medullary cystic kidney disease linked to 16p12
Authors: Pirulli, D Puzzer, D De Fusco, M Crovella, S Amoroso, A Scolari, F Viola, BF Maiorca, R Caridi, G Savoldi, S Ghiggeri, G Casari, G
Citation: D. Pirulli et al., Molecular analysis of uromodulin and SAH genes, positional candidates for autosomal dominant medullary cystic kidney disease linked to 16p12, J NEPHROL, 14(5), 2001, pp. 392-396
Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis
Authors: Caridi, G Bertelli, R Carrea, A Di Duca, M Catarsi, P Artero, M Carraro, M Zennaro, C Candiano, G Musante, L Seri, M Ginevri, F Perfumo, F Ghiggeri, GM
Citation: G. Caridi et al., Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis, J AM S NEPH, 12(12), 2001, pp. 2742-2746
Juvenile nephronophthisis and related variants: Clinical features and molecular approach
Authors: Caridi, G Dagnino, M Miglietti, N Carrea, A Perfumo, F Gusmano, R Ghiggeri, GM
Citation: G. Caridi et al., Juvenile nephronophthisis and related variants: Clinical features and molecular approach, CONTR NEPHR, 136, 2001, pp. 57-67
Medullary cystic kidney disease: Past and present
Authors: Scolari, F Viola, BF Prati, E Ghiggeri, GM Caridi, G Amoroso, A Casari, G Maiorca, R
Citation: F. Scolari et al., Medullary cystic kidney disease: Past and present, CONTR NEPHR, 136, 2001, pp. 68-78
Improved strategy for molecular genetic diagnostics in juvenile nephronophthisis
Authors: Heninger, E Otto, E Imm, A Caridi, G Hildebrandt, F
Citation: E. Heninger et al., Improved strategy for molecular genetic diagnostics in juvenile nephronophthisis, AM J KIDNEY, 37(6), 2001, pp. 1131-1139
IgA nephropathy, the most common cause of glomerulonephritis, is linked to6q22-23
Authors: Gharavi, AG Yan, Y Scolari, F Schena, FP Frasca, GM Ghiggeri, GM Cooper, K Amoroso, A Viola, BF Battini, G Caridi, G Canova, C Farhi, A Subramanian, V Nelson-Williams, C Woodford, S Julian, BA Wyatt, RJ Lifton, RP
Citation: Ag. Gharavi et al., IgA nephropathy, the most common cause of glomerulonephritis, is linked to6q22-23, NAT GENET, 26(3), 2000, pp. 354-357
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes
Authors: Seri, M Cusano, R Gangarossa, S Caridi, G Bordo, D Lo Nigro, C Ghiggeri, GM Ravazzolo, R Savino, M Del Vecchio, M d'Apolito, M Iolascon, A Zelante, LL Savoia, A Balduini, CL Noris, P Magrini, U Belletti, S
Citation: M. Seri et al., Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes, NAT GENET, 26(1), 2000, pp. 103-105
Localisation of the gene responsible for Fechtner syndrome in a region < 600 Kb on 22q11-q13
Authors: Cusano, R Gangarossa, S Forabosco, P Caridi, G Ghiggeri, GM Russo, G Iolascon, A Ravazzolo, R Seri, M
Citation: R. Cusano et al., Localisation of the gene responsible for Fechtner syndrome in a region < 600 Kb on 22q11-q13, EUR J HUM G, 8(11), 2000, pp. 895-899
Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney disease
Authors: Kroiss, S Huck, K Berthold, S Ruschendorf, F Scolari, F Caridi, G Ghiggeri, GM Hildebrant, F Fuchshuber, A
Citation: S. Kroiss et al., Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney disease, NEPH DIAL T, 15(6), 2000, pp. 818-821
Clinical and molecular heterogeneity of juvenile nephronophthisis in Italy: Insights from molecular screening
Authors: Caridi, G Dagnino, M Gusmano, R Ginevri, F Murer, L Ghio, L Piaggio, G Ciardi, MR Perfumo, F Ghiggeri, GM
Citation: G. Caridi et al., Clinical and molecular heterogeneity of juvenile nephronophthisis in Italy: Insights from molecular screening, AM J KIDNEY, 35(1), 2000, pp. 44-51
A DNA element in the alpha 1 type III collagen promoter mediates a stimulatory response by angiotensin II
Authors: Ghiggeri, GM Oleggini, R Musante, L Caridi, G Gusmano, R Ravazzolo, R
Citation: Gm. Ghiggeri et al., A DNA element in the alpha 1 type III collagen promoter mediates a stimulatory response by angiotensin II, KIDNEY INT, 58(2), 2000, pp. 537-548
Exclusion of the candidate genes ACE and Bcl-2 for six families with nephronophthisis not linked to the NPH1 locus
Authors: Omran, H Haffner, K Vollmer, M Pigulla, J Wagner, G Caridi, G Hildebrandt, F
Citation: H. Omran et al., Exclusion of the candidate genes ACE and Bcl-2 for six families with nephronophthisis not linked to the NPH1 locus, NEPH DIAL T, 14(10), 1999, pp. 2328-2331
N-(4-hydroxphenyl) retinamide inhibits cystogenesis by polycystic epithelial cell lines in vitro
Authors: Altieri, P Caridi, G Chiesa, V Ponzoni, M Ghiggeri, GM
Citation: P. Altieri et al., N-(4-hydroxphenyl) retinamide inhibits cystogenesis by polycystic epithelial cell lines in vitro, LIFE SCI, 64(22), 1999, pp. PL259-PL265
Identification of a new locus for medullary cystic disease, on chromosome 16p12
Authors: Scolari, F Puzzer, D Amoroso, A Caridi, G Ghiggeri, GM Maiorca, R Aridon, P De Fusco, M Ballabio, A Casari, G
Citation: F. Scolari et al., Identification of a new locus for medullary cystic disease, on chromosome 16p12, AM J HU GEN, 64(6), 1999, pp. 1655-1660
Renal-retinal syndromes: Association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locus
Authors: Caridi, G Murer, L Bellantuono, R Sorino, P Caringella, DA Gusmano, R Ghiggeri, GM
Citation: G. Caridi et al., Renal-retinal syndromes: Association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locus, AM J KIDNEY, 32(6), 1998, pp. 1059-1062
Risultati: 1-15 |