Ghiggeri GM - Search Results

1

IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23.

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. Gharavi AG, et al. Among authors: ghiggeri gm. Nat Genet. 2000 Nov;26(3):354-7. doi: 10.1038/81677. Nat Genet. 2000. PMID: 11062479

2

Mapping of the human COL5A1 gene to chromosome 9q34.3.

Caridi G, Pezzolo A, Bertelli R, Gimelli G, Di Donato A, Candiano G, Ghiggeri GM. Caridi G, et al. Among authors: ghiggeri gm. Hum Genet. 1992 Sep-Oct;90(1-2):174-6. doi: 10.1007/BF00210769. Hum Genet. 1992. PMID: 1427773

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

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

6

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.

7

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.

8

Identification of a new locus for medullary cystic disease, on chromosome 16p12.

Scolari F, Puzzer D, Amoroso A, Caridi G, Ghiggeri GM, Maiorca R, Aridon P, De Fusco M, Ballabio A, Casari G. Scolari F, et al. Among authors: ghiggeri gm. Am J Hum Genet. 1999 Jun;64(6):1655-60. doi: 10.1086/302414. Am J Hum Genet. 1999. PMID: 10330352 Free PMC article.

9

Clinical and molecular heterogeneity of juvenile nephronophthisis in Italy: insights from molecular screening.

Caridi G, Dagnino M, Gusmano R, Ginevri F, Murer L, Ghio L, Piaggio G, Ciardi MR, Perfumo F, Ghiggeri GM. Caridi G, et al. Among authors: ghiggeri gm. Am J Kidney Dis. 2000 Jan;35(1):44-51. doi: 10.1016/S0272-6386(00)70300-3. Am J Kidney Dis. 2000. PMID: 10620543

10

Evidence of further genetic heterogeneity in autosomal dominant medullary cystic kidney disease.

Kroiss S, Huck K, Berthold S, Rüschendorf F, Scolari F, Caridi G, Ghiggeri GM, Hildebrandt F, Fuchshuber A. Kroiss S, et al. Among authors: ghiggeri gm. Nephrol Dial Transplant. 2000 Jun;15(6):818-21. doi: 10.1093/ndt/15.6.818. Nephrol Dial Transplant. 2000. PMID: 10831633

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