Schepis C - Search Results

1

Cutis tricolor: a literature review and report of five new cases.

Ruggieri M, Polizzi A, Schepis C, Morano M, Strano S, Belfiore G, Palmucci S, Foti PV, Pirrone C, Roggini M, David E, Salpietro V, Milone P. Ruggieri M, et al. Among authors: schepis c. Quant Imaging Med Surg. 2016 Oct;6(5):525-534. doi: 10.21037/qims.2016.10.14. Quant Imaging Med Surg. 2016. PMID: 27942472 Free PMC article.

2

Mixed vascular nevus syndrome: a report of four new cases and a literature review.

Ruggieri M, Polizzi A, Strano S, Schepis C, Morano M, Belfiore G, Palmucci S, Foti PV, Pirrone C, Sofia V, David E, Salpietro V, Mankad K, Milone P. Ruggieri M, et al. Among authors: schepis c. Quant Imaging Med Surg. 2016 Oct;6(5):515-524. doi: 10.21037/qims.2016.10.09. Quant Imaging Med Surg. 2016. PMID: 27942471 Free PMC article.

3

Neurological manifestations in individuals with pure cutaneous or syndromic (Ruggieri-Happle syndrome) phenotypes with "cutis tricolor": a study of 14 cases.

Lionetti E, Pavone P, Kennerknecht I, Failla G, Schepis C, De Pasquale R, Pavone L, Ruggieri M. Lionetti E, et al. Among authors: schepis c. Neuropediatrics. 2010 Aug;41(2):60-5. doi: 10.1055/s-0030-1261919. Epub 2010 Aug 26. Neuropediatrics. 2010. PMID: 20799151

4

Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform.

Calì F, Chiavetta V, Ruggeri G, Piccione M, Selicorni A, Palazzo D, Bonsignore M, Cereda A, Elia M, Failla P, Figura MG, Fiumara A, Maitz S, Luana Mandarà GM, Mattina T, Ragalmuto A, Romano C, Ruggieri M, Salluzzo R, Saporoso A, Schepis C, Sorge G, Spanò M, Tortorella G, Romano V. Calì F, et al. Among authors: schepis c. Eur J Med Genet. 2017 Feb;60(2):93-99. doi: 10.1016/j.ejmg.2016.11.001. Epub 2016 Nov 9. Eur J Med Genet. 2017. PMID: 27838393

5

Milia-like idiopathic calcinosis cutis: an unusual dermatosis associated with Down syndrome.

Schepis C, Siragusa M, Palazzo R, Batolo D, Romano C. Schepis C, et al. Br J Dermatol. 1996 Jan;134(1):143-6. Br J Dermatol. 1996. PMID: 8745902 Review.

6

Hypomelanosis of Ito: electron microscopical observations on two new cases.

Cavallari V, Ussia AF, Siragusa M, Schepis C. Cavallari V, et al. Among authors: schepis c. J Dermatol Sci. 1996 Oct;13(1):87-92. doi: 10.1016/0923-1811(95)00507-2. J Dermatol Sci. 1996. PMID: 8902659

7

Facies: the value of an old diagnostic tip in pediatric dermatology.

Schepis C, Romano C. Schepis C, et al. G Ital Dermatol Venereol. 2018 Oct;153(5):716-721. doi: 10.23736/S0392-0488.17.05626-7. Epub 2017 Apr 19. G Ital Dermatol Venereol. 2018. PMID: 28421730 Review.

8

Exome sequencing in a child with neurodevelopmental disorder and epilepsy: Variant analysis of the AHNAK2 gene.

Vinci M, Kursula P, Greco D, Elia M, Vetri L, Schepis C, Chiavetta V, Donadio S, Roccella M, Carotenuto M, Romano V, Calì F. Vinci M, et al. Among authors: schepis c. Mol Genet Genomic Med. 2022 Sep;10(9):e2012. doi: 10.1002/mgg3.2012. Epub 2022 Jul 5. Mol Genet Genomic Med. 2022. PMID: 35789128 Free PMC article.

9

Multiplex ligation-dependent probe amplification detection of an unknown large deletion of the CREB-binding protein gene in a patient with Rubinstein-Taybi syndrome.

Calì F, Failla P, Chiavetta V, Ragalmuto A, Ruggeri G, Schinocca P, Schepis C, Romano V, Romano C. Calì F, et al. Among authors: schepis c. Genet Mol Res. 2013 Jan 7;12(3):2809-15. doi: 10.4238/2013.January.7.2. Genet Mol Res. 2013. PMID: 23315884 Free article.

10

An endocrinological study of patients with primary cutis verticis gyrata.

Palazzo R, Schepis C, Ruggeri M, Baldini L, Pizzimenti A, Arcoraci V, Spina E. Palazzo R, et al. Among authors: schepis c. Acta Derm Venereol. 1993 Oct;73(5):348-9. doi: 10.2340/0001555573348349. Acta Derm Venereol. 1993. PMID: 7904399 Free article.

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