Cristina Chelleri

9PUBLICATIONS
38CO-AUTHORS
Cancer diagnosisNeurology and neuromuscular diseasesGene mappingImmunogenetics (incl. genetic immunology)
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Publications (9)

|May 14, 2025
Café-Au-Lait Macules in Neurofibromatosis Type 1: Birthmark or Biomarker?

Andrea Santangelo, Cristina Chelleri, Marco Tomasino

|Apr 14, 2025
Somatic Double Inactivation of NF1 Associated with NF1-Related Pectus Excavatum Deformity.

Cristina Chelleri, Marcello Scala, Patrizia De Marco

|Jul 20, 2024
Novel causative variants in Legius syndrome: SPRED1 Genotype spectrum expansion.

Cristina Chelleri, Noemi Brolatti, Patrizia De Marco

|Mar 28, 2024
Dermatologic Effects of Selumetinib in Pediatric Patients with Neurofibromatosis Type 1: Clinical Challenges and Therapeutic Management.

Paola Borgia, Gianluca Piccolo, Andrea Santangelo

|Mar 29, 2023
Moyamoya Vasculopathy in Neurofibromatosis Type 1 Pediatric Patients: The Role of Rare Variants of RNF213.

Marzia Ognibene, Marcello Scala, Michele Iacomino

|Apr 30, 2021
Genotype-Phenotype Correlations in Neurofibromatosis Type 1: A Single-Center Cohort Study.

Marcello Scala, Irene Schiavetti, Francesca Madia

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