Binni F - Search Results

1

Homozygous p.M172K mutation of the TFR2 gene in an Italian family with type 3 hereditary hemochromatosis and early onset iron overload.

Majore S, Milano F, Binni F, Stuppia L, Cerrone A, Tafuri A, De Bernardo C, Palka G, Grammatico P. Majore S, et al. Among authors: binni f. Haematologica. 2006 Aug;91(8 Suppl):ECR33. Haematologica. 2006. PMID: 16923517

2

Radio FC, Majore S, Binni F, Valiante M, Ricerca BM, De Bernardo C, Morrone A, Grammatico P. Radio FC, et al. Among authors: binni f. Blood Cells Mol Dis. 2014 Feb-Mar;52(2-3):83-7. doi: 10.1016/j.bcmd.2013.08.003. Epub 2013 Sep 20. Blood Cells Mol Dis. 2014. PMID: 24055163

3

HAMP gene mutation c.208T>C (p.C70R) identified in an Italian patient with severe hereditary hemochromatosis.

Majore S, Binni F, Pennese A, De Santis A, Crisi A, Grammatico P. Majore S, et al. Among authors: binni f. Hum Mutat. 2004 Apr;23(4):400. doi: 10.1002/humu.9232. Hum Mutat. 2004. PMID: 15024747

4

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: binni f. Haematologica. 2002 Feb;87(2):221-2. Haematologica. 2002. PMID: 11836175

5

ATP2C1 gene mutation analysis in Italian patients with Hailey-Hailey disease.

Majore S, Biolcati G, Barboni L, Cannistraci C, Binni F, Crisi A, Picardo M, Grammatico P. Majore S, et al. Among authors: binni f. J Invest Dermatol. 2005 Nov;125(5):933-5. doi: 10.1111/j.0022-202X.2005.23941.x. J Invest Dermatol. 2005. PMID: 16297192 Free article.

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: binni f. Melanoma Res. 2001 Oct;11(5):447-9. doi: 10.1097/00008390-200110000-00002. Melanoma Res. 2001. PMID: 11595880

7

Novel and recurrent p14 mutations in Italian familial melanoma.

Binni F, Antigoni I, De Simone P, Majore S, Silipo V, Crisi A, Amantea A, Pacchiarini D, Castori M, De Bernardo C, Catricalà C, Grammatico P. Binni F, et al. Clin Genet. 2010 Jun;77(6):581-6. doi: 10.1111/j.1399-0004.2009.01298.x. Epub 2010 Feb 4. Clin Genet. 2010. PMID: 20132244

8

Type 3 hereditary hemochromatosis in a patient from sub-Saharan Africa: is there a link between African iron overload and TFR2 dysfunction?

Majore S, Ricerca BM, Radio FC, Binni F, Cosentino I, Gallusi G, De Bernardo C, Morrone A, Grammatico P. Majore S, et al. Among authors: binni f. Blood Cells Mol Dis. 2013 Jan;50(1):31-2. doi: 10.1016/j.bcmd.2012.08.007. Epub 2012 Sep 11. Blood Cells Mol Dis. 2013. PMID: 22981443 No abstract available.

9

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: binni f. Cancer Genet Cytogenet. 2008 Apr 15;182(2):130-5. doi: 10.1016/j.cancergencyto.2008.01.009. Cancer Genet Cytogenet. 2008. PMID: 18406876

10

Paradoxical association of extensive nevus flammeus together with unilateral lower limb and breast hypoplasia.

Castori M, Majore S, Binni F, Grammatico P. Castori M, et al. Among authors: binni f. Am J Med Genet A. 2009 Feb;149A(2):266-7. doi: 10.1002/ajmg.a.32591. Am J Med Genet A. 2009. PMID: 19133697 No abstract available.

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