Ghiggeri GM - Search Results

1

Mutations in DSTYK and dominant urinary tract malformations.

Sanna-Cherchi S, Sampogna RV, Papeta N, Burgess KE, Nees SN, Perry BJ, Choi M, Bodria M, Liu Y, Weng PL, Lozanovski VJ, Verbitsky M, Lugani F, Sterken R, Paragas N, Caridi G, Carrea A, Dagnino M, Materna-Kiryluk A, Santamaria G, Murtas C, Ristoska-Bojkovska N, Izzi C, Kacak N, Bianco B, Giberti S, Gigante M, Piaggio G, Gesualdo L, Vukic DK, Vukojevic K, Saraga-Babic M, Saraga M, Gucev Z, Allegri L, Latos-Bielenska A, Casu D, State M, Scolari F, Ravazzolo R, Kiryluk K, Al-Awqati Q, D'Agati VD, Drummond IA, Tasic V, Lifton RP, Ghiggeri GM, Gharavi AG. Sanna-Cherchi S, et al. Among authors: ghiggeri gm. N Engl J Med. 2013 Aug 15;369(7):621-9. doi: 10.1056/NEJMoa1214479. Epub 2013 Jul 17. N Engl J Med. 2013. PMID: 23862974 Free PMC article.

2

Modulation of proteinuria and renal xanthine oxidase activity by dietary proteins in acute adriamycin nephrosis in rats: lack of correlation with intra- and extracellular amino acids.

Canepa A, Ghiggeri GM, Carrea A, Ginevri F, Trivelli A, Perfumo F, Gusmano R. Canepa A, et al. Among authors: ghiggeri gm. Nephron. 1992;60(3):342-8. doi: 10.1159/000186776. Nephron. 1992. PMID: 1565188

3

A new biallelic DNA polymorphism of the human COL5A1 gene.

Cappa F, Caridi G, Gimelli G, Ghiggeri GM. Cappa F, et al. Among authors: ghiggeri gm. Hum Genet. 1995 May;95(5):599-600. doi: 10.1007/BF00223882. Hum Genet. 1995. PMID: 7759090

4

Are the nail-patella syndrome and the autosomal Goltz-like syndrome the phenotypic expressions of different alleles at the COL5A1 locus?

Ghiggeri GM, Caridi G, Altieri P, Pezzolo A, Gimelli G, Zuffardi O. Ghiggeri GM, et al. Hum Genet. 1993 Mar;91(2):175-7. doi: 10.1007/BF00222720. Hum Genet. 1993. PMID: 8462976

5

Regulation by TGF-beta and bFGF of ECM expression by PKD cells 'in culture'.

Altieri P, Caridi G, Ghiggeri GM, Garberi A, Ginevri F, Perfumo F, Gusmano R. Altieri P, et al. Among authors: ghiggeri gm. Contrib Nephrol. 1995;115:122-6. Contrib Nephrol. 1995. PMID: 8585898 No abstract available.

6

Cell-specific regulation of alpha1(III) and alpha2(V) collagen by TGF-beta1 in tubulointerstitial cell models.

Bertelli R, Valenti F, Oleggini R, Caridi G, Altieri P, Coviello DA, Botti G, Ravazzolo R, Ghiggeri GM. Bertelli R, et al. Among authors: ghiggeri gm. Nephrol Dial Transplant. 1998 Mar;13(3):573-9. doi: 10.1093/ndt/13.3.573. Nephrol Dial Transplant. 1998. PMID: 9550630

7

Expression of collagen by renal fibroblasts treated with FK 506 in vitro.

Ginevri F, Gusmano R, Altieri P, Valenti F, Oleggini R, Giampuzzi M, Caridi G, Ravazzolo R, Ghiggeri GM. Ginevri F, et al. Among authors: ghiggeri gm. Transplant Proc. 1998 Jun;30(4):957-8. doi: 10.1016/s0041-1345(98)00109-2. Transplant Proc. 1998. PMID: 9636387 No abstract available.

8

Autosomal dominant medullary cystic disease: a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus.

Scolari F, Ghiggeri GM, Casari G, Amoroso A, Puzzer D, Caridi GL, Valzorio B, Tardanico R, Vizzardi V, Savoldi S, Viola BF, Bossini N, Prati E, Gusmano R, Maiorca R. Scolari F, et al. Among authors: ghiggeri gm. Nephrol Dial Transplant. 1998 Oct;13(10):2536-46. doi: 10.1093/ndt/13.10.2536. Nephrol Dial Transplant. 1998. PMID: 9794556

9

Nephronophthisis-medullary cystic disease: clinical and genetic aspects.

Gusmano R, Ghiggeri GM, Caridi G. Gusmano R, et al. Among authors: ghiggeri gm. J Nephrol. 1998 Sep-Oct;11(5):224-8. J Nephrol. 1998. PMID: 9831234 Review.

10

Renal-retinal syndromes: association of retinal anomalies and recessive nephronophthisis in patients with homozygous deletion of the NPH1 locus.

Caridi G, Murer L, Bellantuono R, Sorino P, Caringella DA, Gusmano R, Ghiggeri GM. Caridi G, et al. Among authors: ghiggeri gm. Am J Kidney Dis. 1998 Dec;32(6):1059-62. doi: 10.1016/s0272-6386(98)70083-6. Am J Kidney Dis. 1998. PMID: 9856524 Review.

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