Cristina Chelleri
Genoa, 16132, Italy
Last Updated: 09/26/2026
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Found 12 publications
Café-Au-Lait Macules in Neurofibromatosis Type 1: Birthmark or Biomarker?
Journal: Cancers
Published: February 14, 2025
Novel causative variants in Legius syndrome: SPRED1 Genotype spectrum expansion.
Journal: American journal of medical genetics. Part A
Published: March 20, 2024
Dermatologic Effects of Selumetinib in Pediatric Patients with Neurofibromatosis Type 1: Clinical Challenges and Therapeutic Management.
Journal: Journal of clinical medicine
Published: February 15, 2024
Somatic Double Inactivation of NF1 Associated with NF1-Related Pectus Excavatum Deformity.
Journal: Human mutation
Published: November 03, 2022
Case report: Revascularization failure in NF1-related moyamoya syndrome after selumetinib: A possible pathophysiological correlation?
Journal: Frontiers in pediatrics
Published: September 22, 2022
RNF213 variant in a patient with Legius syndrome associated with moyamoya syndrome.
Journal: Molecular genetics & genomic medicine
Published: May 03, 2021
Genotype-Phenotype Correlations in Neurofibromatosis Type 1: A Single-Center Cohort Study.
Journal: Cancers
Published: March 05, 2021
Acute hemorrhagic edema: Uncommon features.
Journal: Journal of the American Academy of Dermatology
Published: July 02, 2020
Anterior chest wall deformities in children with neurofibromatosis type 1.
Journal: Acta paediatrica (Oslo, Norway : 1992)
Published: July 01, 2020
Residual Lesions After Pharmacological and Dye-Laser Treatment of Infantile Hemangiomas: Critical Review of 432 Cases.
Journal: Lasers in surgery and medicine
Published: November 28, 2019
Plaque-type glomuvenous malformations in a child.
Journal: Lancet (London, England)
Published: July 28, 2015
Showing 1-12 of 12
Last Updated: 09/26/2026