A. Papi

No patient is the same; lessons learned from antibody repertoire profiling in hospitalized severe COVID-19 patients

M. V. van Gils, J. Snijder, S. Spadaro, 2022, medRxiv.

Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran

H. Galehdari, M. Zamani, A. Sedaghat, 2022, Molecular genetics & genomic medicine.

A Novel Missense Mutation in the EDAR Gene and One Missense Mutation in EDA Gene in the Study of HED Patients in Iran

H. Galehdari, G. Shariati, S. Khatami, 2021, Iranian Journal of Pediatrics.