Caridi G - Search Results

1

Association of the macrophage migration inhibitory factor -173*C allele with childhood nephrotic syndrome.

Vivarelli M, D'Urbano LE, Stringini G, Ghiggeri GM, Caridi G, Donn R, Tozzi A, Emma F, De Benedetti F. Vivarelli M, et al. Among authors: caridi g. Pediatr Nephrol. 2008 May;23(5):743-8. doi: 10.1007/s00467-007-0729-2. Epub 2008 Jan 29. Pediatr Nephrol. 2008. PMID: 18228042

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. 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: caridi g. 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. Among authors: caridi g. 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: caridi g. Contrib Nephrol. 1995;115:122-6. Contrib Nephrol. 1995. PMID: 8585898 No abstract available.

6

Nephronophthisis-medullary cystic disease: clinical and genetic aspects.

Gusmano R, Ghiggeri GM, Caridi G. Gusmano R, et al. Among authors: caridi g. 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. 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

Juvenile nephronophthisis and related variants: clinical features and molecular approach.

Caridi G, Dagnino M, Miglietti N, Carrea A, Perfumo F, Gusmano R, Ghiggeri GM. Caridi G, et al. Contrib Nephrol. 2001;(136):57-67. doi: 10.1159/000060179. Contrib Nephrol. 2001. PMID: 11688404 Review. No abstract available.

9

Medullary cystic kidney disease: past and present.

Scolari F, Viola BF, Prati E, Ghiggeri GM, Caridi G, Amoroso A, Casari G, Maiorca R. Scolari F, et al. Among authors: caridi g. Contrib Nephrol. 2001;(136):68-78. doi: 10.1159/000060180. Contrib Nephrol. 2001. PMID: 11688405 Review. No abstract available.

10

Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.

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. Caridi G, et al. J Am Soc Nephrol. 2001 Dec;12(12):2742-2746. doi: 10.1681/ASN.V12122742. J Am Soc Nephrol. 2001. PMID: 11729243

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