C. Schepis

发表

Anetoderma Secondary to the Application of Leeches

D. Batolo, M. Siragusa, C. Schepis, 1996, International journal of dermatology.

A de novo mutation of KRT1 in a baby girl causing epidermolytic ichthyosis with impressive epidermolytic palmoplantar keratoderma.

F. Calì, M. Vinci, P. Failla, 2020, Dermatology online journal.

Nervous system involvement in Degos disease.

M. Elia, F. Cosentino, C. Amato, 2005, AJNR. American journal of neuroradiology.

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

A. Polizzi, V. Salpietro, M. Ruggieri, 2016, Quantitative imaging in medicine and surgery.

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

A. Polizzi, V. Salpietro, M. Ruggieri, 2016, Quantitative imaging in medicine and surgery.

Cockayne syndrome and lichen actinicus

G. Fabrizi, C. Schepis, R. Palazzo, 1994 .

Nevus Sebaceous Syndrome

A. Polizzi, F. Lacarrubba, A. Verzì, 2018, Journal of Pediatric Neurology.

Diagnostic pathology and description of a new SPINK 5 variant

F. Calì, M. Vinci, A. Centofanti, 2019 .

Skin ulcers in a young woman on low‐dose estrogen‐combination pill

C. Schepis, A. Alberti, A. Alberti, 1997, International journal of dermatology.

An Updated Survey on Skin Conditions in Down Syndrome

R. Pettinato, C. Romano, C. Barone, 2002, Dermatology.

Multiple melanonychia as a sign of pituitary adenoma

B. Piraccini, M. Siragusa, C. Schepis, 2013, Clinical and experimental dermatology.

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

F. Calì, M. Elia, V. Romano, 2022, Molecular genetics & genomic medicine.

Perforating Milia‐like Idiopathic Calcinosis Cutis and Periorbital Syringomas in a Girl With Down Syndrome

C. Romano, D. Batolo, M. Siragusa, 1994, Pediatric dermatology.

Macular Amyloidosis due to Friction by a Horsehair Glove

V. Cavallari, M. Siragusa, C. Schepis, 2000, Dermatology.

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

C. Romano, D. Batolo, M. Siragusa, 1996, The British journal of dermatology.

LOCALIZED ELASTOSIS PERFORANS SERPIGINOSA IN A BOY WITH DOWN SYNDROME

C. Romano, V. Cavallari, M. Siragusa, 1997, Pediatric dermatology.

A huge malodorous lesion on the scalp.

M. Lentini, C. Schepis, 2012, The American Journal of dermatopathology.

Eruptive Syringomas with Calcium Deposits in a Young Woman with Down’s Syndrome

V. Cavallari, M. Siragusa, C. Schepis, 2001, Dermatology.

Secondary anetoderma in people with Down's syndrome.

M. Siragusa, C. Schepis, 1999, Acta dermato-venereologica.

Prevalence of atopic dermatitis in patients with Down syndrome: a clinical survey.

C. Romano, C. Barone, M. Siragusa, 1997, Journal of the American Academy of Dermatology.

Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Becker's Nevus Syndrome

A. Polizzi, F. Lacarrubba, A. Verzì, 2018, Journal of Pediatric Neurology.

Schimmelpenning Syndrome: A Kind of Craniofacial Epidermal Nevus Associated with Cerebral and Ocular MR Imaging Abnormalities

M. Elia, C. Amato, C. Schepis, 2010, American Journal of Neuroradiology.

Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome)

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Cerebriform plantar hyperplasia: the major cutaneous feature of Proteus syndrome

C. Romano, D. Greco, M. Siragusa, 2008, International journal of dermatology.

Rubinstein–Taybi Syndrome with Epidermal Nevus: A Case Report

C. Romano, D. Greco, D. Batolo, 2001, Pediatric dermatology.

A teen-ager with linear atrophoderma of Moulin.

M. Lentini, C. Schepis, R. Palazzo, 2010, Dermatology online journal.

White fibrous papulosis of the neck in three Sicilian patients

D. Batolo, M. Siragusa, C. Schepis, 1996, The Australasian journal of dermatology.

Palpebral syringomas and Down's syndrome.

G. Fabrizi, G. Massi, M. Siragusa, 1994, Dermatology.

A CASE OF FG SYNDROME WITH GINGIVAL HYPERPLASIA AND KELOIDS

C. Romano, M. Elia, C. Schepis, 1995, Pediatric dermatology.

Failure of fluoxetine to modify the skin‐picking behaviour of Prader‐Willi syndrome

C. Romano, P. Failla, M. Siragusa, 1998, The Australasian journal of dermatology.

SKIN‐PICKING: THE BEST CUTANEOUS FEATURE IN THE RECOGNIZATION OF PRADER‐WILLI SYNDROME

C. Romano, P. Failla, M. Siragusa, 1994, International journal of dermatology.

Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome)

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Failure of colchicine in the treatment of severe acne vulgaris.

A. P. Guerra, M. Siragusa, C. Schepis, 1999, Acta dermato-venereologica.

Progressive Cribriform and Zosteriform Hyperpigmentation: The Late-Onset Feature of Linear and Whorled Nevoid Hypermelanosis Associated with Congenital Neurological, Skeletal and Cutaneous Anomalies

C. Romano, M. Siragusa, C. Schepis, 1999, Dermatology.

AN ADDITIONAL CASE OF LINEAR AND WHORLED NEVOID HYPERMELANOSIS ASSOCIATED WITH BIRTH DEFECTS AND MENTAL RETARDATION

C. Romano, V. Cavallari, M. Siragusa, 1999, Pediatric dermatology.

CUTANEOUS FINDINGS IN THE MENTALLY RETARDED

C. Romano, C. Schepis, CARMELO SCHEPIS, 1996, International journal of dermatology.

Erosive lichen planus: two uncommon cases.

M. Lentini, M. Siragusa, C. Schepis, 2008, Acta dermato-venereologica.

Nail pathology in patients with hemiplegia

F. Cosentino, R. Spada, M. Siragusa, 2001, The British journal of dermatology.

Correspondence: A case of prurigo pigmentosa successfully treated with minocycline

M. Siragusa, C. Schepis, 2000 .

Prurigo pigmentosa treated with minocycline

V. Cavallari, M. Siragusa, C. Schepis, 1996, The British journal of dermatology.

Longitudinal red streaks on the big toenails in a patient with pseudobulbar syndrome

M. Siragusa, C. Schepis, S. Del Gracco, 2001, Journal of the European Academy of Dermatology and Venereology : JEADV.

Mees' lines due to cyclosporin.

M. Siragusa, C. Schepis, A. Alberti, 1999, The British journal of dermatology.

Mixed Vascular Nevus Syndrome

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Wyburn-Mason Syndrome

A. Polizzi, M. Ruggieri, Elena Commodari, 2018, Journal of Pediatric Neurology.

Tuberous sclerosis complex

E. Henske, S. Jóźwiak, J. C. Kingswood, 2016, Nature Reviews Disease Primers.

The papulokeratotic type of solitary benign lichenoid keratosis

D. Batolo, M. Lentini, C. Schepis, 2003, International journal of dermatology.

Tenascin expression in actinic keratosis

D. Batolo, M. Lentini, C. Schepis, 2006, Journal of cutaneous pathology.

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

V. Cavallari, M. Siragusa, C. Schepis, 1996, Journal of dermatological science.

Aninteresting case of Piebaldism with café-au-lait macules and freckling: the use of targeted next-generation sequencing for molecular diagnosis

F. Calì, P. Failla, V. Chiavetta, 2018, European Journal of Dermatology.

Cutaneous findings in children with intellectual disabilities

C. Schepis, 2013, The Journal of dermatology.

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

C. Romano, F. Calì, M. Bonsignore, 2017, European journal of medical genetics.

Prevalence of primary cutis verticis gyrata in a psychiatric population: association with chromosomal fragile sites.

S. Cannavò, E. Spina, C. Barletta, 1990, Acta Dermato-Venereologica.

ASSOCIATION OF CUTIS VERTICIS GYRATA WITH FRAGILE X SYNDROME AND FRAGILITY OF CHROMOSOME 12

E. Spina, C. Barletta, C. Schepis, 1989, The Lancet.

Prominent neurological involvement in Dercum disease

Mariagiovanna Cantone, R. Ferri, G. Lanza, 2017, Journal of Neurology.

Primary cutis verticis gyrata or pachydermia verticis gyrata: a peculiar scalp disorder of mentally retarded adult males.

M. Siragusa, C. Schepis, 1995, Dermatology.

An endocrinological study of patients with primary cutis verticis gyrata.

L. Baldini, E. Spina, V. Arcoraci, 1993, Acta dermato-venereologica.

Blue Rubber Bleb Nevus Syndrome

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Phacomatosis Pigmentokeratotica

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Phacomatosis Pigmentovascularis

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Speckled Lentiginous Nevus Syndrome

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome)

A. Polizzi, F. Lacarrubba, G. Micali, 2018, Journal of Pediatric Neurology.

Hypomelanosis of Ito

A. Polizzi, S. Savasta, F. Lacarrubba, 1981, Journal of Pediatric Neurology.

PTEN Gene: A Model for Genetic Diseases in Dermatology

C. Romano, C. Schepis, 2012, TheScientificWorldJournal.

Review Article Pten Gene: a Model for Genetic Diseases in Dermatology 1. Pten Gene: What It Is and How It Works

C. Romano, C. Schepis, 2022 .

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

I. Kennerknecht, M. Ruggieri, P. Pavone, 2010, Neuropediatrics.

A. Polizzi, I. Kennerknecht, F. Lacarrubba, 2018, Journal of Pediatric Neurology.

Cutis Tricolor (Ruggieri-Happle Syndrome)

I. Kennerknecht, M. Ruggieri, P. Iannetti, 2008 .

An intriguing case of LEOPARD syndrome.

C. Romano, D. Greco, D. Batolo, 1998 .

A small blackberry-like nodule on the nipple in a pregnant affected by Tuberous Sclerosis Complex.

M. Bottitta, M. Lentini, M. Siragusa, 2019, Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia.

A new patient with idiopathic tripe palms.

D. Batolo, M. Siragusa, C. Schepis, 1997, Acta dermato-venereologica.

ACE-Inhibitor-Induced Drug Eruption Resembling Lymphocytic Infiltration (of Jessner-Kanof) and Lupus erythematosus tumidus

D. Batolo, M. Lentini, M. Siragusa, 2004, Dermatology.

Prurigo pigmentosa: a misdiagnosed dermatitis in Sicily.

V. Cavallari, M. Siragusa, C. Schepis, 1999, Cutis.

Alopecia areata in Down syndrome: a clinical evaluation

C. Romano, C. Barone, C. Schepis, 2005, Journal of the European Academy of Dermatology and Venereology : JEADV.

A New Case of Trichothiodystrophy Associated with Autism, Seizures, and Mental Retardation

M. Elia, M. Barbareschi, M. Siragusa, 1997, Pediatric dermatology.

Degos’ Disease (Malignant Atrophic Papulosis)

C. Amato, M. Ruggieri, M. Siragusa, 2008 .

Two siblings affected by Netherton/Comèl syndrome. Diagnostic pathology and description of a new SPINK5 variant.

F. Calì, M. Vinci, A. Centofanti, 2019, Dermatology Online Journal.

Long faun tail: a rare cutaneous marker of spinal dysraphism.

M. Elia, C. Amato, C. Schepis, 2016, Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia.

Novel SPINK5 variants in a patient with Netherton syndrome and intellectual disability. The diagnostic value of trichoscopy.

F. Calì, M. Vinci, P. Failla, 2020, Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia.

Cognitive Impairment in Inpatients with Prurigo Nodularis and Psychiatric Comorbidities

R. Ferri, B. Lanuzza, G. Lanza, 2021, International journal of environmental research and public health.

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

V. Cavallari, M. Siragusa, C. Schepis, 2001, European journal of dermatology : EJD.

An unusual location of nodular elastosis with cysts and comedones (Favre-Racouchot's disease).

D. Batolo, M. Siragusa, C. Schepis, 2000, Acta dermato-venereologica.

Eruptive seborrheic keratoses and chronic lymphoid leukemia: the Leser‐Trélat sign

G. Fabrizi, M. Siragusa, C. Schepis, 1994 .

Piezogenic pedal papules during Prader–Willi syndrome

C. Romano, D. Greco, M. Siragusa, 2005, Journal of the European Academy of Dermatology and Venereology : JEADV.

Primary macular amyloidosis: an ultrastructural approach to diagnosis.

V. Cavallari, M. Siragusa, C. Schepis, 1999, Ultrastructural pathology.

An Intriguing Case of LEOPARD Syndrome

C. Romano, D. Greco, D. Batolo, 1998, Pediatric dermatology.

Skin pathology findings in a cohort of 1500 adult and elderly subjects

R. Spada, G. Fabrizi, B. Guarneri, 1999, International journal of dermatology.

An odd precocious case of progressive osseous heteroplasia

F. Calì, M. Lentini, C. Schepis, 2021, Italian Journal of Dermatology and Venereology.

A new family with Papillon-Lefèvre syndrome: effectiveness of etretinate treatment.

C. Romano, D. Batolo, N. Batticane, 2000, Cutis.

Erosive lichen planus on an atypical site mimicking a factitial dermatitis.

M. Lentini, M. Siragusa, C. Schepis, 2010, Acta dermato-venereologica.

A Multiplex PCR-Based Next-Generation Sequencing Approach Has Detected a Common Large Deletion in STS Gene in a Patient with X-Linked Ichthyosis

C. Romano, F. Calì, V. Romano, 2016 .

Medial Telangiectatic Sacral Nevi (Types A and C) Associated with Williams Syndrome

P. Bosco, C. Romano, A. Ragusa, 2000, Dermatology.

Medial Telangiectatic Sacral Nevi and Mca/Mr Syndromes

C. Romano, A. Sindoni, P. Failla, 2003, Pediatric dermatology.

Cryotherapy as a Precipitant Factor in Focal and Segmental Dystonia

A. Alberti, C. Romano, M. Siragusa, 1999, Dermatology.

The Burden of Autosomal Recessive Congenital Ichthyoses on Patients and their Families: An Italian Multicentre Study

C. Bodemer, D. Bonamonte, A. Filoni, 2021, Acta dermato-venereologica.

Psoriasis and alopecia areata in a Down syndrome patient: a Renbök phenomenon

R. Happle, M. Siragusa, C. Schepis, 2017, European Journal of Dermatology.

Cryotherapy as a Precipitant Factor in Focal and Segmental Dystonia

A. Alberti, M. Siragusa, C. Schepis, 1999, Dermatology.