Alessandro De Falco

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 15

Top Topics

Endoplasmic Reticulum

Top Venues

American journal of medical genetics. Part A

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

Publications

Elia Marco Paolo Minale, Alessandro De Falco, Emanuele Agolini, Antonio Novelli, Roberta Russo, Immacolata Andolfo, Achille Iolascon, Carmelo Piscopo
First Case of a Dominant De Novo SEC23A Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature Review. Genes 15 (1) (2024)
Elia Marco Paolo Minale, Alessandro De Falco, Emanuele Agolini, Antonio Novelli, Roberta Russo, Immacolata Andolfo, Achille Iolascon, Carmelo Piscopo
First Case of a Dominant De Novo SEC23A Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature Review. Genes 15 (1) (2024)
Alessandro De Falco, Antonella Gambale, Michele Pinelli, Teresa Suero, Luigia De Falco, Achille Iolascon, Stefania Martone
Trisomy 21 with Maternally Inherited Balanced Translocation (15q;22q) in a Female Fetus: A Rare Case of Probable Interchromosomal Effect. Cells 13 (13) (2024)
Elia Marco Paolo Minale, Alessandro De Falco, Emanuele Agolini, Antonio Novelli, Roberta Russo, Immacolata Andolfo, Achille Iolascon, Carmelo Piscopo
First Case of a Dominant De Novo SEC23A Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature Review. Genes 15 (1) (2024)
Elia Marco Paolo Minale, Alessandro De Falco, Emanuele Agolini, Antonio Novelli, Roberta Russo, Immacolata Andolfo, Achille Iolascon, Carmelo Piscopo
First Case of a Dominant De Novo SEC23A Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature Review. Genes 15 (1) (2024)
Alessandro De Falco, Antonella Gambale, Michele Pinelli, Teresa Suero, Luigia De Falco, Achille Iolascon, Stefania Martone
Trisomy 21 with Maternally Inherited Balanced Translocation (15q;22q) in a Female Fetus: A Rare Case of Probable Interchromosomal Effect. Cells 13 (13) (2024)
Alessandro De Falco, Daniele De Brasi, Matteo Della Monica, Claudia Cesario, Stefano Petrocchi, Antonio Novelli, Giuseppe D'Alterio, Achille Iolascon, Mario Capasso, Carmelo Piscopo
A Novel Variant in RAD21 in Cornelia De Lange Syndrome Type 4: Case Report and Bioinformatic Analysis. Genes 14 (1) (2023)
Alessandro De Falco, Marianthi Karali, Chiara Criscuolo, Francesco Testa, Maria Rosaria Barillari, Margherita Scarpato, Valeria Gaudieri, Alberto Cuocolo, Anna Russo, Vincenzo Nigro, Francesca Simonelli, Sandro Banfi, Nicola Brunetti-Pierri
Late-onset mucopolysaccharidosis type IIIA mimicking Usher syndrome. American journal of medical genetics. Part A 194 (5) (2023)
Alessandro De Falco, Daniele De Brasi, Matteo Della Monica, Claudia Cesario, Stefano Petrocchi, Antonio Novelli, Giuseppe D'Alterio, Achille Iolascon, Mario Capasso, Carmelo Piscopo
A Novel Variant in RAD21 in Cornelia De Lange Syndrome Type 4: Case Report and Bioinformatic Analysis. Genes 14 (1) (2023)
Alessandro De Falco, Marianthi Karali, Chiara Criscuolo, Francesco Testa, Maria Rosaria Barillari, Margherita Scarpato, Valeria Gaudieri, Alberto Cuocolo, Anna Russo, Vincenzo Nigro, Francesca Simonelli, Sandro Banfi, Nicola Brunetti-Pierri
Late-onset mucopolysaccharidosis type IIIA mimicking Usher syndrome. American journal of medical genetics. Part A (2023)
Alessandro De Falco, Marianthi Karali, Chiara Criscuolo, Francesco Testa, Maria Rosaria Barillari, Margherita Scarpato, Valeria Gaudieri, Alberto Cuocolo, Anna Russo, Vincenzo Nigro, Francesca Simonelli, Sandro Banfi, Nicola Brunetti-Pierri
Late-onset mucopolysaccharidosis type IIIA mimicking Usher syndrome. American journal of medical genetics. Part A 194 (5) (2023)
Alessandro De Falco, Marianthi Karali, Chiara Criscuolo, Francesco Testa, Maria Rosaria Barillari, Margherita Scarpato, Valeria Gaudieri, Alberto Cuocolo, Anna Russo, Vincenzo Nigro, Francesca Simonelli, Sandro Banfi, Nicola Brunetti-Pierri
Late-onset mucopolysaccharidosis type IIIA mimicking Usher syndrome. American journal of medical genetics. Part A 194 (5) (2023)
Alessandro De Falco, Daniele De Brasi, Matteo Della Monica, Claudia Cesario, Stefano Petrocchi, Antonio Novelli, Giuseppe D'Alterio, Achille Iolascon, Mario Capasso, Carmelo Piscopo
A Novel Variant in RAD21 in Cornelia De Lange Syndrome Type 4: Case Report and Bioinformatic Analysis. Genes 14 (1) (2023)
Alessandro De Falco, Daniele De Brasi, Matteo Della Monica, Claudia Cesario, Stefano Petrocchi, Antonio Novelli, Giuseppe D'Alterio, Achille Iolascon, Mario Capasso, Carmelo Piscopo
A Novel Variant in RAD21 in Cornelia De Lange Syndrome Type 4: Case Report and Bioinformatic Analysis. Genes 14 (1) (2023)
Alessandro De Falco, Achille Iolascon, Flora Ascione, Carmelo Piscopo
New Insights in 9q21.13 Microdeletion Syndrome: Genotype-Phenotype Correlation of 28 Patients. Genes 14 (5) (2023)