Barbara Scelsa

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 8

Top Venues

Diagnostics (Basel, Switzerland)

Neurology. Genetics

Molecular genetics & genomic medicine

Cerebellum (London, England)

Ospedale dei Bambini Vittore Buzzi

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Ospedale dei Bambini Vittore Buzzi

Italy

senior consultant :: pediatric neurology

Publications

Mario Tortora, Elisa Cattaneo, Luigina Spaccini, Maria Iascone, Barbara Scelsa, Alessia Micalizzi, Antonio Novelli, Mariano Lanna, Andrea Righini, Pierangelo Veggiotti, Chiara Doneda
Novel Genetic Variant in HUWE1 : Prenatal and Postnatal Neuroimaging Phenotype. Neurology. Genetics 10 (4) (2024)
Mario Tortora, Elisa Cattaneo, Luigina Spaccini, Maria Iascone, Barbara Scelsa, Alessia Micalizzi, Antonio Novelli, Mariano Lanna, Andrea Righini, Pierangelo Veggiotti, Chiara Doneda
Novel Genetic Variant in HUWE1 : Prenatal and Postnatal Neuroimaging Phenotype. Neurology. Genetics 10 (4) (2024)
Chiara Ionio, Gianluca Lista, Pierangelo Veggiotti, Caterina Colombo, Giulia Ciuffo, Irene Daniele, Marta Landoni, Barbara Scelsa, Enrico Alfei, Stefania Maria Bova
Cognitive, Behavioral and Socioemotional Development in a Cohort of Preterm Infants at School Age: A Cross-Sectional Study. Pediatric reports 14 (1) (2022)
Barbara Scelsa
Fetal Neurology: From Prenatal Counseling to Postnatal Follow-Up. Diagnostics (Basel, Switzerland) 12 (12) (2022)
Barbara Scelsa
Fetal Neurology: From Prenatal Counseling to Postnatal Follow-Up. Diagnostics (Basel, Switzerland) 12 (12) (2022)
Barbara Scelsa, Gianni Cutillo, Mariano Matteo Lanna, Andrea Righini, Marina Antonella Balestriero, Valeria Brazzoduro, Stefania Zambrano, Cecilia Parazzini, Enrico Alfei, Mariangela Rustico
Prenatal Diagnosis and Neurodevelopmental Outcome in Isolated Cerebellar Hypoplasia of Suspected Hemorrhagic Etiology: a Retrospective Cohort Study. Cerebellum (London, England) (2021)
Francesca Cogliati, Valentina Giorgini, Maura Masciadri, Maria Teresa Bonati, Margherita Marchi, Irene Cracco, Davide Gentilini, Angela Peron, Miriam Nella Savini, Luigina Spaccini, Barbara Scelsa, Silvia Maitz, Edvige Veneselli, Giulia Prato, Maria Pintaudi, Isabella Moroni, Aglaia Vignoli, Lidia Larizza, Silvia Russo
Pathogenic Variants in STXBP1 and in Genes for GABAa Receptor Subunities Cause Atypical Rett/Rett-like Phenotypes. International journal of molecular sciences 20 (15) (2019)
Barbara Scelsa, Serena Gasperini, Andrea Righini, Maria Iascone, Valeria G Brazzoduro, Pierangelo Veggiotti
Mild phenotype in Molybdenum cofactor deficiency: A new patient and review of the literature. Molecular genetics & genomic medicine 7 (6) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Barbara Scelsa