Floriana Secondulfo

Publication Activity (10 Years)

Years Active: 2023-2023
Publications (10 Years): 5

Top Topics

Autism Spectrum Disorder

Fluorescence Imaging

Patient Reported Outcomes

Top Venues

Therapeutics and clinical risk management

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

Publications

Andrea Melluso, Floriana Secondulfo, Giovanna Capolongo, Giovambattista Capasso, Miriam Zacchia
Bardet-Biedl Syndrome: Current Perspectives and Clinical Outlook. Therapeutics and clinical risk management 19 (2023)
Miriam Zacchia, Giovanna Capolongo, Francesca Del Vecchio Blanco, Floriana Secondulfo, Neha Gupta, Giancarlo Blasio, Rosa Maria Pollastro, Angela Cervesato, Giulio Piluso, Giuseppe Gigliotti, Anna Laura Torella, Vincenzo Nigro, Alessandra Fortunata Perna, Giovambattista Capasso, Francesco Trepiccione
Next-Generation Sequencing (NGS) Analysis Illustrates the Phenotypic Variability of Collagen Type IV Nephropathies. Genes 14 (3) (2023)
Miriam Zacchia, Giovanna Capolongo, Francesca Del Vecchio Blanco, Floriana Secondulfo, Neha Gupta, Giancarlo Blasio, Rosa Maria Pollastro, Angela Cervesato, Giulio Piluso, Giuseppe Gigliotti, Anna Laura Torella, Vincenzo Nigro, Alessandra Fortunata Perna, Giovambattista Capasso, Francesco Trepiccione
Next-Generation Sequencing (NGS) Analysis Illustrates the Phenotypic Variability of Collagen Type IV Nephropathies. Genes 14 (3) (2023)
Andrea Melluso, Floriana Secondulfo, Giovanna Capolongo, Giovambattista Capasso, Miriam Zacchia
Bardet-Biedl Syndrome: Current Perspectives and Clinical Outlook. Therapeutics and clinical risk management 19 (2023)
Miriam Zacchia, Giovanna Capolongo, Francesca Del Vecchio Blanco, Floriana Secondulfo, Neha Gupta, Giancarlo Blasio, Rosa Maria Pollastro, Angela Cervesato, Giulio Piluso, Giuseppe Gigliotti, Anna Laura Torella, Vincenzo Nigro, Alessandra Fortunata Perna, Giovambattista Capasso, Francesco Trepiccione
Next-Generation Sequencing (NGS) Analysis Illustrates the Phenotypic Variability of Collagen Type IV Nephropathies. Genes 14 (3) (2023)