Grammatico P - Search Results

1

Identification of a novel duplication in the APC gene using multiple ligation probe amplification in a patient with familial adenomatous polyposis.

Pedace L, Majore S, Megiorni F, Binni F, De Bernardo C, Antigoni I, Preziosi N, Mazzilli MC, Grammatico P. Pedace L, et al. Among authors: grammatico p. Cancer Genet Cytogenet. 2008 Apr 15;182(2):130-5. doi: 10.1016/j.cancergencyto.2008.01.009. Cancer Genet Cytogenet. 2008. PMID: 18406876

2

Identification of APC gene mutations in Italian adenomatous polyposis coli patients by PCR-SSCP analysis.

Varesco L, Gismondi V, James R, Robertson M, Grammatico P, Groden J, Casarino L, De Benedetti L, Bafico A, Bertario L, et al. Varesco L, et al. Among authors: grammatico p. Am J Hum Genet. 1993 Feb;52(2):280-5. Am J Hum Genet. 1993. PMID: 8381581 Free PMC article.

3

APC gene mutations in Italian familial polyposis coli patients.

Varesco L, Gismondi V, James R, De Benedetti L, Heouaine A, Biticchi R, Masetti E, Bertario L, Sala P, Grammatico P, et al. Varesco L, et al. Among authors: grammatico p. Cancer Detect Prev. 1993;17(2):279-81. Cancer Detect Prev. 1993. PMID: 8402712

4

Trisomy 20 in a papillary urothelial carcinoma of the ureter.

Grammatico P, Lombardo A, Governatori M, Mordenti C, Poscente M, Del Porto G. Grammatico P, et al. Cancer Genet Cytogenet. 1996 Sep;90(2):132-4. doi: 10.1016/s0165-4608(96)90071-0. Cancer Genet Cytogenet. 1996. PMID: 8830722

5

Dot-and-fleck retinopathy in Alport syndrome caused by a novel mutation in the COL4A5 gene.

Blasi MA, Rinaldi R, Renieri A, Petrucci R, De Bernardo C, Bruttini M, Grammatico P. Blasi MA, et al. Among authors: grammatico p. Am J Ophthalmol. 2000 Jul;130(1):130-1. doi: 10.1016/s0002-9394(00)00466-9. Am J Ophthalmol. 2000. PMID: 11004279

6

CDKN2A novel mutation in a patient from a melanoma-prone family.

Grammatico P, Binni F, Eibenschutz L, De Bernardo C, Grammatico B, Rinaldi R, De Simone P, Catricalà C. Grammatico P, et al. Among authors: grammatico b. Melanoma Res. 2001 Oct;11(5):447-9. doi: 10.1097/00008390-200110000-00002. Melanoma Res. 2001. PMID: 11595880

7

Absence of hepcidin gene mutations in 10 Italian patients with primary iron overload.

Majore S, Binni F, Ricerca BM, Brioli G, Grammatico P. Majore S, et al. Among authors: grammatico p. Haematologica. 2002 Feb;87(2):221-2. Haematologica. 2002. PMID: 11836175

8

Cytogenetic and molecular characterization of a de novo 4q24qter duplication and correlation to the associated phenotype.

Rinaldi R, De Bernardo C, Assumma M, Grammatico B, Buffone E, Poscente M, Grammatico P. Rinaldi R, et al. Among authors: grammatico p, grammatico b. Am J Med Genet A. 2003 Apr 15;118A(2):122-6. doi: 10.1002/ajmg.a.10093. Am J Med Genet A. 2003. PMID: 12655492 Review.

9

Clinical management and molecular cytogenetic characterization in a 45,X/46,X,idic(Yp) patient with severe hypospadia.

Marrocco G, Poscente M, Majore S, De Bernardo C, Rinaldi R, Del Porto G, Storniello G, Grammatico P. Marrocco G, et al. Among authors: grammatico p. J Pediatr Surg. 2003 Aug;38(8):1258-62. doi: 10.1016/s0022-3468(03)00284-7. J Pediatr Surg. 2003. PMID: 12891509

10

CDKN2A: the IVS2-105A/G intronic mutation found in an Italian patient affected by eight primary melanomas.

Majore S, Catricalà C, Binni F, De Simone P, Eibenschutz L, Grammatico P. Majore S, et al. Among authors: grammatico p. J Invest Dermatol. 2004 Feb;122(2):450-1. doi: 10.1046/j.0022-202X.2004.22222.x. J Invest Dermatol. 2004. PMID: 15009729 Free article. No abstract available.

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