Del Porto G - Search Results

1

Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 families.

Zachara E, Caforio AL, Carboni GP, Pellegrini A, Pompili A, Del Porto G, Sciarra A, Bosman C, Boldrini R, Prati PL, et al. Zachara E, et al. Among authors: del porto g. Br Heart J. 1993 Feb;69(2):129-35. doi: 10.1136/hrt.69.2.129. Br Heart J. 1993. PMID: 8435238 Free PMC article.

2

Autosomal dominant simple microphthalmos.

Vingolo EM, Steindl K, Forte R, Zompatori L, Iannaccone A, Sciarra A, Del Porto G, Pannarale MR. Vingolo EM, et al. Among authors: del porto g. J Med Genet. 1994 Sep;31(9):721-5. doi: 10.1136/jmg.31.9.721. J Med Genet. 1994. PMID: 7815444 Free PMC article.

3

Unusual vascular malformation of the kidney in both twins of a monozygotic pair: short case report.

Mastroberardino G, Sciarra A, Gualtieri R, Di Fusco C, Grammatico P, Del Porto G. Mastroberardino G, et al. Among authors: del porto g. Acta Genet Med Gemellol (Roma). 1987;36(4):567-70. doi: 10.1017/s000156600000698x. Acta Genet Med Gemellol (Roma). 1987. PMID: 3454522

4

Variable number of tandem repeats in zygosity diagnosis in twins.

Costanzi Porrini S, Sciarra A, Sulli N, Piane M, Gualtieri R, Del Porto G. Costanzi Porrini S, et al. Among authors: del porto g. Acta Genet Med Gemellol (Roma). 1990;39(4):473-7. doi: 10.1017/s000156600000369x. Acta Genet Med Gemellol (Roma). 1990. PMID: 1983279

5

20 p duplication as a result of parental translocation: familial case report and a contribution to the clinical delineation of the syndrome.

Grammatico P, Cupilari F, Di Rosa C, Falcolini M, Del Porto G. Grammatico P, et al. Among authors: del porto g. Clin Genet. 1992 Jun;41(6):285-9. doi: 10.1111/j.1399-0004.1992.tb03398.x. Clin Genet. 1992. PMID: 1623622

6

Autosomal-dominant retinitis pigmentosa associated with an Arg-135-Trp point mutation of the rhodopsin gene. Clinical features and longitudinal observations.

Pannarale MR, Grammatico B, Iannaccone A, Forte R, DeBernardo C, Flagiello L, Vingolo EM, Del Porto G. Pannarale MR, et al. Among authors: del porto g. Ophthalmology. 1996 Sep;103(9):1443-52. doi: 10.1016/s0161-6420(96)30485-5. Ophthalmology. 1996. PMID: 8841304

7

Clinical heterogeneity of dominant optic atrophy: the contribution of visual function investigations to diagnosis.

Del Porto G, Vingolo EM, Steindl K, Forte R, Iannaccone A, Rispoli E, Pannarale MR. Del Porto G, et al. Graefes Arch Clin Exp Ophthalmol. 1994 Dec;232(12):717-27. doi: 10.1007/BF00184274. Graefes Arch Clin Exp Ophthalmol. 1994. PMID: 7890185

8

The ocular phenotype of the Bardet-Biedl syndrome. Comparison to non-syndromic retinitis pigmentosa.

Iannaccone A, De Propris G, Roncati S, Rispoli E, Del Porto G, Pannarale MR. Iannaccone A, et al. Among authors: del porto g. Ophthalmic Genet. 1997 Mar;18(1):13-26. doi: 10.3109/13816819709057879. Ophthalmic Genet. 1997. PMID: 9134546

9

A twin study of cytogenetic variability. Progress report.

Gedda L, Del Porto G, Brenci G, D'alessandro E, Di Fusco C, Di Tonto B. Gedda L, et al. Among authors: del porto g. Acta Genet Med Gemellol (Roma). 1977;26(3-4):275-6. doi: 10.1017/s0001566000009752. Acta Genet Med Gemellol (Roma). 1977. PMID: 566017 No abstract available.

10

Establishment and characterization of a human neuroblastoma cell line.

Scarpa S, Dominici C, Grammatico P, Del Porto G, Raschellà G, Castello M, Forni G, Modesti A. Scarpa S, et al. Among authors: del porto g. Int J Cancer. 1989 Apr 15;43(4):645-51. doi: 10.1002/ijc.2910430418. Int J Cancer. 1989. PMID: 2703273

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