T. D’Andrea

Prenatal diagnosis of congenital heart disease and fetal karyotyping.

D. Paladini, R. Calabro', S. Palmieri, 1993, Obstetrics and gynecology.

Human iPSC Modeling of Genetic Febrile Seizure Reveals Aberrant Molecular and Physiological Features Underlying an Impaired Neuronal Activity

G. Cuda, A. Gambardella, E. Parrotta, 2022, Biomedicines.

Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility

E. Bacchelli, E. Maestrini, A. Posar, 2022, Frontiers in Psychiatry.

Selective Reduction of Ca2+ Entry Through the Human NMDA Receptor: a Quantitative Study by Simultaneous Ca2+ and Na+ Imaging.

S. Fucile, Maria Cristina Benedetti, T. D’Andrea, 2024, Molecular neurobiology.

Cortical neurons obtained from patient-derived iPSCs with GNAO1 p.G203R variant show altered differentiation and functional properties

Dosh Whye, G. Tartaglia, M. Lagarkova, 2023, bioRxiv.