R. Noeiaghdam

A rare case of SRD5A3‐CDG in a patient with ataxia and telangiectasia: A case report

Leila Johari, H. Esmaeilzadeh, S. Hosseini, 2022, Clinical case reports.

Homozygous Autosomal Recessive DIAPH1 Mutation Associated with Central Nervous System Involvement and Aspergillosis: A Rare Case

Leila Johari, H. Esmaeilzadeh, S. Hosseini, 2022, Case reports in genetics.

An unusual case of cystic fibrosis with pancytopenia due to copper deficiency and blindness caused by vitamin A deficiency: A case-report

Leila Johari, Z. Kanannejad, H. Esmaeilzadeh, 2022, Respiratory medicine case reports.