Curcio C - Search Results

1

Analysis of the GJB2 and GJB6 genes in Italian patients with nonsyndromic hearing loss: frequencies, novel mutations, genotypes, and degree of hearing loss.

Primignani P, Trotta L, Castorina P, Lalatta F, Sironi F, Radaelli C, Degiorgio D, Curcio C, Travi M, Ambrosetti U, Cesarani A, Garavelli L, Formigoni P, Milani D, Murri A, Cuda D, Coviello DA. Primignani P, et al. Among authors: curcio c. Genet Test Mol Biomarkers. 2009 Apr;13(2):209-17. doi: 10.1089/gtmb.2008.0086. Genet Test Mol Biomarkers. 2009. PMID: 19371219

2

A novel dominant missense mutation--D179N--in the GJB2 gene (Connexin 26) associated with non-syndromic hearing loss.

Primignani P, Castorina P, Sironi F, Curcio C, Ambrosetti U, Coviello DA. Primignani P, et al. Among authors: curcio c. Clin Genet. 2003 Jun;63(6):516-21. doi: 10.1034/j.1399-0004.2003.00079.x. Clin Genet. 2003. PMID: 12786758

3

The introduction of QF-PCR in prenatal diagnosis of fetal aneuploidies: time for reconsideration.

Nicolini U, Lalatta F, Natacci F, Curcio C, Bui TH. Nicolini U, et al. Among authors: curcio c. Hum Reprod Update. 2004 Nov-Dec;10(6):541-8. doi: 10.1093/humupd/dmh046. Hum Reprod Update. 2004. PMID: 15514017 Review.

4

A new de novo missense mutation in connexin 26 in a sporadic case of nonsyndromic deafness.

Primignani P, Trotta L, Castorina P, Lalatta F, Cuda D, Murri A, Ambrosetti U, Cesarani A, Curcio C, Coviello D, Travi M. Primignani P, et al. Among authors: curcio c. Laryngoscope. 2007 May;117(5):821-4. doi: 10.1097/MLG.0b013e31803330d9. Laryngoscope. 2007. PMID: 17473676

5

Discordant prenatal phenotype and karyotype of monozygotic twins characterized by the unequal distribution of two cell lines investigated by different methods: a review.

Gentilin B, Guerneri S, Bianchi V, Natacci F, Colombo A, Fogliani R, Fortuna R, Coviello DA, Curcio C, Lalatta F. Gentilin B, et al. Among authors: curcio c. Twin Res Hum Genet. 2008 Jun;11(3):352-6. doi: 10.1375/twin.11.3.352. Twin Res Hum Genet. 2008. PMID: 18498214 Review.

6

COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma.

Galbiati S, Monguzzi A, Damin F, Soriani N, Passiu M, Castellani C, Natacci F, Curcio C, Seia M, Lalatta F, Chiari M, Ferrari M, Cremonesi L. Galbiati S, et al. Among authors: curcio c. J Med Genet. 2016 Jul;53(7):481-7. doi: 10.1136/jmedgenet-2015-103229. Epub 2016 Feb 24. J Med Genet. 2016. PMID: 26912453

7

Hemoglobin A₂ and Heterogeneous Diagnostic Relevance Observed in Eight New Variants of the Delta Globin Gene.

Mahmud N, Maffei M, Mogni M, Forni GL, Pinto VM, Barberio G, Ungari S, Maffè A, Curcio C, Zanolli F, Paventa R, Carta M, Caleffi A, Mercadanti M, Maoggi S, Ivaldi G, Coviello D. Mahmud N, et al. Among authors: curcio c. Genes (Basel). 2021 Nov 19;12(11):1821. doi: 10.3390/genes12111821. Genes (Basel). 2021. PMID: 34828427 Free PMC article.

8

Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of beta-thalassemia.

Galbiati S, Foglieni B, Travi M, Curcio C, Restagno G, Sbaiz L, Smid M, Pasi F, Ferrari A, Ferrari M, Cremonesi L. Galbiati S, et al. Among authors: curcio c. Haematologica. 2008 Apr;93(4):610-4. doi: 10.3324/haematol.11895. Epub 2008 Mar 6. Haematologica. 2008. PMID: 18326525 Free article.

9

Hb Milano [α109(G16)Leu→Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the α1-Globin Gene in an Italian Family.

Curcio C, Giannone V, Benzoni E, Cesaretti C, Ivaldi G. Curcio C, et al. Hemoglobin. 2019 Jan;43(1):4-6. doi: 10.1080/03630269.2019.1566138. Epub 2019 May 14. Hemoglobin. 2019. PMID: 31084368

10

Fetal DNA in maternal plasma: a noninvasive tool for prenatal diagnosis of beta-thalassemia.

Galbiati S, Brisci A, Damin F, Gentilin B, Curcio C, Restagno G, Cremonesi L, Ferrari M. Galbiati S, et al. Among authors: curcio c. Expert Opin Biol Ther. 2012 Jun;12 Suppl 1:S181-7. doi: 10.1517/14712598.2012.677428. Epub 2012 Apr 16. Expert Opin Biol Ther. 2012. PMID: 22506923 Review.

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