Ghiggeri GM - Search Results

1

Copy-number disorders are a common cause of congenital kidney malformations.

Sanna-Cherchi S, Kiryluk K, Burgess KE, Bodria M, Sampson MG, Hadley D, Nees SN, Verbitsky M, Perry BJ, Sterken R, Lozanovski VJ, Materna-Kiryluk A, Barlassina C, Kini A, Corbani V, Carrea A, Somenzi D, Murtas C, Ristoska-Bojkovska N, Izzi C, Bianco B, Zaniew M, Flogelova H, Weng PL, Kacak N, Giberti S, Gigante M, Arapovic A, Drnasin K, Caridi G, Curioni S, Allegri F, Ammenti A, Ferretti S, Goj V, Bernardo L, Jobanputra V, Chung WK, Lifton RP, Sanders S, State M, Clark LN, Saraga M, Padmanabhan S, Dominiczak AF, Foroud T, Gesualdo L, Gucev Z, Allegri L, Latos-Bielenska A, Cusi D, Scolari F, Tasic V, Hakonarson H, Ghiggeri GM, Gharavi AG. Sanna-Cherchi S, et al. Among authors: ghiggeri gm. Am J Hum Genet. 2012 Dec 7;91(6):987-97. doi: 10.1016/j.ajhg.2012.10.007. Epub 2012 Nov 15. Am J Hum Genet. 2012. PMID: 23159250 Free PMC article.

2

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

3

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

4

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.

5

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.

6

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.

7

N-(4-hydroxyphenyl) retinamide inhibits cystogenesis by polycystic epithelial cell lines in vitro.

Altieri P, Caridi G, Chiesa V, Ponzoni M, Ghiggeri GM. Altieri P, et al. Among authors: ghiggeri gm. Life Sci. 1999;64(22):PL259-65. doi: 10.1016/s0024-3205(99)00155-1. Life Sci. 1999. PMID: 10374933

8

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

9

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

10

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. Among authors: ghiggeri gm. Contrib Nephrol. 2001;(136):57-67. doi: 10.1159/000060179. Contrib Nephrol. 2001. PMID: 11688404 Review. No abstract available.

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