Author = Nasim Pouralizadeh
Clinical Significance of OATP2 Gene Variants in Iranian Neonates with Hyperbilirubinemia

Volume 13, Issue 1, January 2022, Pages 30-35

10.22038/ijn.2021.57052.2074

Abbas Boskabadi; Gholamali Mamouri; Hassan Boskabadi; Nasim Pouralizadeh; Ali Moradi; Hassan Mehrad-Majd


Genetic Association of UGT1A1 Promoter Variants (c.-3279T>G and c.-3156G>A) with Neonatal Hyperbili-rubinemia in an Iranian Population

Volume 12, Issue 2, April 2021, Pages 63-69

10.22038/ijn.2021.50368.1884

Nasim Pouralizadeh; Gholamali Mamouri; Abbas Boskabadi; Hassan Boskabadi; Houshang Rafatpanah; Ali Moradi; Hassan Mehrad-Majd


A Rare Case of Neonatal Hypophosphatasia: A Case Report

Volume 9, Issue 1, March 2018, Pages 75-77

10.22038/ijn.2018.21593.1248

Nasim Pouralizadeh; Hassan Boskabadi; Gholamali Mamouri