User profiles for C. Schepis

Carmelo Schepis

Direttore UOSD Dermatologia, IRCCS Oasi Maria SS.Troina
Verified email at oasi.en.it
Cited by 1686

[HTML][HTML] Cutis tricolor: a literature review and report of five new cases

M Ruggieri, A Polizzi, C Schepis… - … imaging in medicine …, 2016 - ncbi.nlm.nih.gov
Background Cutis tricolor is a skin abnormality consisting in a combination of congenital
hyper-and hypopigmented skin lesions (in the form of paired macules, patches or streaks) in …

[HTML][HTML] Mixed vascular nevus syndrome: a report of four new cases and a literature review

M Ruggieri, A Polizzi, S Strano, C Schepis… - … Imaging in Medicine …, 2016 - ncbi.nlm.nih.gov
Background Mixed vascular nevus (or nevus vascularis mixtus) represents an admixture of
cutaneous vascular malformations of the telangiectatic type and angiospastic spots of nevus …

An updated survey on skin conditions in Down syndrome

C Schepis, C Barone, M Siragusa, R Pettinato… - Dermatology, 2002 - karger.com
… 3 Schepis C, Barone C, Siragusa M, Romano C: Prevalence of atopic dermatitis in patients
with Down syndrome: A clinical survey. J Am Acad Dermatol 1997;36:1019–1021. 4 Polenghi …

[HTML][HTML] PTEN gene: a model for genetic diseases in dermatology

C Romano, C Schepis - The Scientific World Journal, 2012 - hindawi.com
PTEN gene is considered one of the most mutated tumor suppressor genes in human
cancer, and it’s likely to become the first one in the near future. Since 1997, its involvement in …

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

…, M Ruggieri, R Salluzzo, A Saporoso, C Schepis… - European journal of …, 2017 - Elsevier
… In order to quantify the percentage of mosaicism in the c.808C > T (p.Gln270*) mutation,
we analyzed the sequencing-electropherogram of capillary electrophoresis performed on ABI …

[PDF][PDF] A new family with Papillon-Lefèvre syndrome: effectiveness of etretinate treatment

…, C Romano, N Batticane, D Batolo, C Schepis - CUTIS-NEW …, 2000 - academia.edu
… Fischer J, Blanchet-Bardon C, Prud’homme JF, et al.: Mapping of Papillon-Lefèvre syndrome
to the chromosome 11q 14 region. Eur J Hum Genet 5… Schepis reports no conflict of interest. …

Eruptive syringomas with calcium deposits in a young woman with Down's syndrome

C Schepis, V Torre, M Siragusa, F Albiero… - Dermatology, 2001 - karger.com
Eruptive syringomas are uncommon in the general population. We describe here an 18-year-old
female, affected by Down’s syndrome, who presented with an abrupt eruption of small …

[HTML][HTML] The burden of autosomal recessive congenital ichthyoses on patients and their families: an Italian multicentre study

…, D Bonamonte, A Filoni, C Schepis… - Acta Dermato …, 2021 - ncbi.nlm.nih.gov
Autosomal recessive congenital ichthyoses (ARCI) are characterized by generalized skin
scaling, hyperkeratosis, erythroderma, and disabling features affecting the skin (palmoplantar …

Nail pathology in patients with hemiplegia

M Siragusa, C Schepis, FII Cosentino… - British Journal of …, 2001 - academic.oup.com
Background It is well known that nails can be involved in some diseases of the central
nervous system; however, no systematic study has been carried out in order to evaluate the …

Friction melanosis, friction amyloidosis, macular amyloidosis, towel melanosis: many names for the same clinical entity

…, R FERRI, V Cavallari, C SCHEPIS - European Journal of …, 2001 - jle.com
Macular or friction amyloidosis is a cutaneous entity characterized by a brownish pigmentation
distributed on the skin over bony regions of the trunk and limbs after the use, for many …