Glucose-6-Phosphate Dehydrogenase Deficiency Latest Advances

Exchange Transfussion for the Treatment of Severe Indirect Hyperbilirubinemia Caused by Glucose-6-Phosphate Dehydrogenase Deficiency: A Case Report.

Journal: Fetal and pediatric pathology

Published: September 27, 2025

G6PD deficiency is implicated in Circle of Willis variants in stroke patients and impairs brain vasculature in zebrafish.

Journal: Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism

Published: September 25, 2025

Interesting Case of Celphos Poisoning with G6PD Deficiency: Is There a Correlation?

Journal: The Journal of the Association of Physicians of India

Published: September 16, 2025

Kernicterus in a late preterm infant with overlooked G6PD deficiency.

Journal: BMJ case reports

Published: August 28, 2025

Association Between G6PD Deficiency and Congenital Heart Disease Incidence and Hospital Outcomes.

Journal: Pediatric cardiology

Published: August 23, 2025

Functional evidence for G6PD variant classification from mutational scanning.

Journal: bioRxiv : the preprint server for biology

Published: August 20, 2025

Portable Point-of-Care Device for Dual Detection of Glucose-6-Phosphate Dehydrogenase Deficiency and Hemoglobin in Low-Resource Settings.

Journal: Biosensors

Published: August 07, 2025

Hereditary Spherocytosis: Review of Presentation at Birth.

Journal: Children (Basel, Switzerland)

Published: July 27, 2025

Pyruvate Kinase Deficiency: An Underdiagnosed Cause of Severe Hemolytic Anemia in Iranian Population: Insights From Whole Exome Sequencing of Four Families and Screening of a Population-Specific Database.

Journal: International journal of laboratory hematology

Published: July 17, 2025

Rapid detection of G6PD deficiency SNPs using a novel amplicon-based MinION Sequencing Assay.

Journal: bioRxiv : the preprint server for biology

Published: July 16, 2025

Integrated Approach for Biochemical and Functional Characterization of Six Clinical Variants of Glucose-6-Phosphate Dehydrogenase.

Journal: International journal of molecular sciences

Published: July 16, 2025

Evaluation of pre-analytical and analytical variables affecting galactose-1-phosphate uridyltransferase assay performance in the diagnosis of classical galactosemia.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: July 11, 2025

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Exchange Transfussion for the Treatment of Severe Indirect Hyperbilirubinemia Caused by Glucose-6-Phosphate Dehydrogenase Deficiency: A Case Report.

Exchange Transfussion for the Treatment of Severe Indirect Hyperbilirubinemia Caused by Glucose-6-Phosphate Dehydrogenase Deficiency: A Case Report.

G6PD deficiency is implicated in Circle of Willis variants in stroke patients and impairs brain vasculature in zebrafish.

G6PD deficiency is implicated in Circle of Willis variants in stroke patients and impairs brain vasculature in zebrafish.

Interesting Case of Celphos Poisoning with G6PD Deficiency: Is There a Correlation?

Interesting Case of Celphos Poisoning with G6PD Deficiency: Is There a Correlation?

Kernicterus in a late preterm infant with overlooked G6PD deficiency.

Kernicterus in a late preterm infant with overlooked G6PD deficiency.

Association Between G6PD Deficiency and Congenital Heart Disease Incidence and Hospital Outcomes.

Association Between G6PD Deficiency and Congenital Heart Disease Incidence and Hospital Outcomes.

Functional evidence for G6PD variant classification from mutational scanning.

Functional evidence for G6PD variant classification from mutational scanning.

Portable Point-of-Care Device for Dual Detection of Glucose-6-Phosphate Dehydrogenase Deficiency and Hemoglobin in Low-Resource Settings.

Portable Point-of-Care Device for Dual Detection of Glucose-6-Phosphate Dehydrogenase Deficiency and Hemoglobin in Low-Resource Settings.

Hereditary Spherocytosis: Review of Presentation at Birth.

Hereditary Spherocytosis: Review of Presentation at Birth.

Pyruvate Kinase Deficiency: An Underdiagnosed Cause of Severe Hemolytic Anemia in Iranian Population: Insights From Whole Exome Sequencing of Four Families and Screening of a Population-Specific Database.

Pyruvate Kinase Deficiency: An Underdiagnosed Cause of Severe Hemolytic Anemia in Iranian Population: Insights From Whole Exome Sequencing of Four Families and Screening of a Population-Specific Database.

Rapid detection of G6PD deficiency SNPs using a novel amplicon-based MinION Sequencing Assay.

Rapid detection of G6PD deficiency SNPs using a novel amplicon-based MinION Sequencing Assay.

Integrated Approach for Biochemical and Functional Characterization of Six Clinical Variants of Glucose-6-Phosphate Dehydrogenase.

Integrated Approach for Biochemical and Functional Characterization of Six Clinical Variants of Glucose-6-Phosphate Dehydrogenase.

Evaluation of pre-analytical and analytical variables affecting galactose-1-phosphate uridyltransferase assay performance in the diagnosis of classical galactosemia.

Evaluation of pre-analytical and analytical variables affecting galactose-1-phosphate uridyltransferase assay performance in the diagnosis of classical galactosemia.