Nongnuch Sirachainan

270 Rama VI Road
Ratchathewi, Thailand

Last Updated: 09/26/2026

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Found 129 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

An International Survey on Current Practices of Management of Neonatal Catheter-Associated Venous Thromboembolism: Communication from the ISTH SSC Subcommittee on Pediatric and Neonatal Thrombosis and Hemostasis.

An International Survey on Current Practices of Management of Neonatal Catheter-Associated Venous Thromboembolism: Communication from the ISTH SSC Subcommittee on Pediatric and Neonatal Thrombosis and Hemostasis.

Journal: Journal of thrombosis and haemostasis : JTH

Published: October 09, 2025

An international survey on current practices of management of neonatal catheter-associated venous thromboembolism: communication from the ISTH SSC Subcommittee on Pediatric and Neonatal Thrombosis and Hemostasis.

An international survey on current practices of management of neonatal catheter-associated venous thromboembolism: communication from the ISTH SSC Subcommittee on Pediatric and Neonatal Thrombosis and Hemostasis.

Journal: Journal of thrombosis and haemostasis : JTH

Published: October 09, 2025

Outcomes of hematopoietic stem cell transplantation for pediatric patients with transfusion-dependent thalassemia in Thailand.

Outcomes of hematopoietic stem cell transplantation for pediatric patients with transfusion-dependent thalassemia in Thailand.

Journal: Clinical and experimental pediatrics

Published: September 17, 2025

Five decades of successive establishment of hemophilia care in Thailand.

Five decades of successive establishment of hemophilia care in Thailand.

Journal: Expert review of hematology

Published: March 31, 2025

International Perspectives on Vitamin K Deficiency Bleeding in Infants: A Cross-Sectional Questionnaire-Based Survey.

International Perspectives on Vitamin K Deficiency Bleeding in Infants: A Cross-Sectional Questionnaire-Based Survey.

Journal: Pediatric blood & cancer

Published: March 02, 2025

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

Genetic Mutations of Congenital Red Cell Membrane Defects in Hydrops Fetalis.

Genetic Mutations of Congenital Red Cell Membrane Defects in Hydrops Fetalis.

Journal: Fetal diagnosis and therapy

Published: December 28, 2024

Eltrombopag in combination with immunosuppressive therapy in pediatric severe aplastic anemia: phase 2 ESCALATE trial.

Eltrombopag in combination with immunosuppressive therapy in pediatric severe aplastic anemia: phase 2 ESCALATE trial.

Journal: Blood advances

Published: December 11, 2024

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

Vitamin K deficiency bleeding in children with cholestatic liver disease: a systematic review and meta-analysis.

Vitamin K deficiency bleeding in children with cholestatic liver disease: a systematic review and meta-analysis.

Journal: Research and practice in thrombosis and haemostasis

Published: September 04, 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

Showing 1-12 of 129

Last Updated: 09/26/2026