Alessandro

Molecular Determinants of T Cell Epitope

Ravi V. Kolla, Bjoern Peters, J. Sidney, 2010 .

CHD 3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Joshua C Randall, G. J. Swaminathan, A. Green, 2019 .

Identification of a sex-specific genetic signature in dementia with Lewy bodies: a meta-analysis of genome-wide association studies

John X. Morris, Elisabet, Sonja W. Scholz, 2022, medRxiv.

A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy

Mauro, E. Gregorio, G. Vaula, 2009, Journal of Neurology, Neurosurgery, and Psychiatry.

Pre‐S2 defective hepatitis B virus infection in patients with fulminant hepatitis

E. Tanzi, G. Raimondo, L. Sagliocca, 1997, Hepatology.