Praguywan Kadegasem

270 Rama VI Road
Ratchathewi, Thailand

Last Updated: 09/26/2026

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Found 46 publications

Screening of hereditary elliptocytosis caused by SPTB mutations and identification of its association with significant jaundice among Thai neonates.

Screening of hereditary elliptocytosis caused by SPTB mutations and identification of its association with significant jaundice among Thai neonates.

Journal: BMJ paediatrics open

Published: March 26, 2026

Measures of cellular oxidative damage following vitamin E supplementation in young patients with transfusion-dependent thalassemia: a double-blind randomized controlled trial.

Measures of cellular oxidative damage following vitamin E supplementation in young patients with transfusion-dependent thalassemia: a double-blind randomized controlled trial.

Journal: BMC pediatrics

Published: January 08, 2025

mBAT: a newly developed mobile application for self-screening of pediatric bleeding disorders - a multi-center study.

mBAT: a newly developed mobile application for self-screening of pediatric bleeding disorders - a multi-center study.

Journal: Annals of hematology

Published: October 09, 2024

Unraveling the Molecular Pathogenesis of Protein C Deficiency-Associated VTE: Insights from Protein C Mutations C238G and R189W in Thai Patients.

Unraveling the Molecular Pathogenesis of Protein C Deficiency-Associated VTE: Insights from Protein C Mutations C238G and R189W in Thai Patients.

Journal: Thrombosis and haemostasis

Published: September 03, 2024

The First Thai Case of Nondeletional HbH Disease Caused by Compound Heterozygosity for α-Thalassemia-1 Chiang Rai (--CR) Type Deletion with Hb Constant Spring.

The First Thai Case of Nondeletional HbH Disease Caused by Compound Heterozygosity for α-Thalassemia-1 Chiang Rai (--CR) Type Deletion with Hb Constant Spring.

Journal: Hemoglobin

Published: August 23, 2024

Efficacy and Safety of a Dispersible Tablet of GPO-Deferasirox Monotherapy among Children with Transfusion-Dependent Thalassemia and Iron Overload.

Efficacy and Safety of a Dispersible Tablet of GPO-Deferasirox Monotherapy among Children with Transfusion-Dependent Thalassemia and Iron Overload.

Journal: Hemoglobin

Published: February 19, 2024

Alleviated bleeding phenotypes in a child with severe haemophilia A and thalassemia disease.

Alleviated bleeding phenotypes in a child with severe haemophilia A and thalassemia disease.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: August 14, 2023

Multicenter Study of Diagnostic Tool for Patients with Hemophilia: From Bedside to Comprehensive Investigations.

Multicenter Study of Diagnostic Tool for Patients with Hemophilia: From Bedside to Comprehensive Investigations.

Journal: The application of clinical genetics

Published: August 08, 2023

One-step amplification refractory mutation system-PCR/high-resolution melting curve assay for carrier detection of red blood cell membranopathy caused by common SPTB mutations.

One-step amplification refractory mutation system-PCR/high-resolution melting curve assay for carrier detection of red blood cell membranopathy caused by common SPTB mutations.

Journal: International journal of laboratory hematology

Published: July 06, 2023

Effectiveness of monthly low dose emicizumab prophylaxis without 4-week loading doses among patients with haemophilia A with and without inhibitors: A case series report.

Effectiveness of monthly low dose emicizumab prophylaxis without 4-week loading doses among patients with haemophilia A with and without inhibitors: A case series report.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: September 02, 2022

Three-Decade Successive Establishment of Care for Women/Girls from Families with Haemophilia.

Three-Decade Successive Establishment of Care for Women/Girls from Families with Haemophilia.

Journal: The application of clinical genetics

Published: July 21, 2022

Whole-exome sequencing uncovered genetic diagnosis of severe inherited haemolytic anaemia: Correlation with clinical phenotypes.

Whole-exome sequencing uncovered genetic diagnosis of severe inherited haemolytic anaemia: Correlation with clinical phenotypes.

Journal: British journal of haematology

Published: March 07, 2022

Showing 1-12 of 46

Last Updated: 09/26/2026