C. Carbonara

Homozygous familial hypercholesterolemia in a young woman with dual gene mutations of low-density lipoprotein receptor and proprotein convertase subtilisin/kexin type 9.

A. Ciavarella, C. Sabbà, P. Suppressa, 2020, Journal of clinical lipidology.

Neonatal cutaneous disseminated aspergillosis in a preterm extremely-low-birth-weight infant with favourable outcome at 3-year follow-up: a case report.

M. Mostert, E. Mastretta, P. Manzoni, 2012, Early human development.

Congenital analbuminemia in a patient affected by hypercholesterolemia: A case report

F. Lugani, C. Sabbà, M. Campagnoli, 2019, World journal of clinical cases.