Roberta Rotunno
Rome, Italy
Last Updated: 09/26/2026
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Found 34 publications
Clinical and Dermoscopic Diagnosis of Actinic Keratosis.
Journal: Dermatology practical & conceptual
Published: June 30, 2024
Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study.
Journal: Biomedicines
Published: January 29, 2022
Expanding the spectrum of Gorham Stout disease exploring a single center pediatric case series.
Journal: Lymphology
Published: January 24, 2022
Management of Upper Airway Infantile Hemangiomas: Experience of One Italian Multidisciplinary Center.
Journal: Frontiers in pediatrics
Published: May 30, 2021
A multicenter study on quality of life of the "greater patient" in congenital ichthyoses.
Journal: Orphanet journal of rare diseases
Published: May 03, 2021
PIK3CA-related overgrowth with an uncommon phenotype: case report.
Journal: Italian journal of pediatrics
Published: April 29, 2021
Ectodermal Dysplasia-Syndactyly Syndrome with Toe-Only Minimal Syndactyly Due to a Novel Mutation in NECTIN4: A Case Report and Literature Review.
Journal: Genes
Published: April 01, 2021
Self-improving dominant dystrophic epidermolysis bullosa: phenotypic variability associated with COL7A1 mutation p.Gly2037Glu.
Journal: European journal of dermatology : EJD
Published: January 18, 2021
First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses.
Journal: International journal of molecular sciences
Published: August 21, 2020
Cutaneous Infantile Haemangiomas with Intracranial and Intraspinal Involvement: A European Multicentre Experience and Review.
Journal: Acta dermato-venereologica
Published: August 01, 2020
Cutaneous venous malformations as a clue for possible gastrointestinal tract involvement: Diagnosis and treatment of six cases.
Journal: Dermatologic therapy
Published: July 15, 2020
Last Updated: 09/26/2026