Clinical Significance of OATP2 Gene Variants in Iranian Neonates with Hyperbilirubinemia
Background: Neonatal hyperbilirubinemia is a life-threatening and multifactorial disorder affecting about 60%-80% of newborns during their first week of life. Various environmental and genetic factors can contribute to the occurrence of this problem. The present study aimed to investigate the relati...
Saved in:
Main Authors: | Abbas Boskabadi (Author), Gholamali Mamouri (Author), Hassan Boskabadi (Author), Nasim Pouralizadeh (Author), Ali Moradi (Author), Hassan Mehrad-Majd (Author) |
---|---|
Format: | Book |
Published: |
Mashhad University of Medical Sciences,
2022-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Genetic Association of UGT1A1 Promoter Variants (c.-3279T>G and c.-3156G>A) with Neonatal Hyperbili-rubinemia in an Iranian Population
by: Nasim Pouralizadeh, et al.
Published: (2021) -
A Rare Case of Neonatal Hypophosphatasia: A Case Report
by: Nasim Pouralizadeh, et al.
Published: (2018) -
Neonates with Covid-19 infection: Is there any different treatment process?
by: Manizhe Pakdel, et al.
Published: (2022) -
Corticosteroid therapy for liver abscesses in a neonate with Chronic granulomatous disease
by: Azadeh Darabi, et al.
Published: (2021) -
Risk Factors and Causes of Neonatal Hyperbilirubinemia: A Systematic Review Study
by: Hassan Boskabadi, et al.
Published: (2020)