Cristina Chelleri
9PUBLICATIONS
38CO-AUTHORS
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Publications (9)
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|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
|May 03, 2021
RNF213 variant in a patient with Legius syndrome associated with moyamoya syndrome.Giulia Romanisio, Cristina Chelleri, Marcello Scala
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Frequent Collaborators
7 joint publications
Maria Cristina Diana
6 joint publications
Marcello Scala
4 joint publications
Pasquale Striano
4 joint publications
Gianluca Piccolo
3 joint publications
Patrizia De Marco
3 joint publications
Marco Pavanello
3 joint publications
Francesca Madia
2 joint publications
Michele Torre
2 joint publications
Simona Baldassari
2 joint publications
Francesco Caroli
