Maria Teresa Falco (Mariateresa Falco)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2021
Publications (10 Years): 3

Top Topics

Magnetic Resonance

Genome Wide Identification

Intellectual Disability

Autism Spectrum Disorder

Top Venues

American journal of medical genetics. Part A

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

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

Publications

Maria Giovanna Tedesco, Fortunato Lonardo, Caterina Ceccarini, Carla Cesarano, Maria Cristina Digilio, Monia Magliozzi, Daniela Rogaia, Amedea Mencarelli, Chiara Leoni, Carmelo Piscopo, Valentina Imperatore, Maria Teresa Falco, Paolo Fontana, Anna Maria Nardone, Antonio Novelli, Stefania Troiani, Marco Seri, Paolo Prontera
Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype. American journal of medical genetics. Part A 185 (4) (2021)
Alessandra D'Amico, Maria Brunella Cipullo, Maria Teresa Falco, Lorenzo Ugga, Daniela Melis
Clinical report of a brain magnetic resonance imaging finding in Noonan syndrome. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 37 (12) (2021)
Maria Teresa Falco, Annamaria Franzè, Sandra Iossa, Luigia De Falco, Antonella Gambale, Elio Marciano, Achille Iolascon
Novel compound heterozygous mutations in BCS1L gene causing Bjornstad syndrome in two siblings. American journal of medical genetics. Part A 173 (5) (2017)