Noppawan Tangbubpha
Bangkok, Thailand
Last Updated: 09/26/2026
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Found 9 publications
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
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.
Journal: International journal of laboratory hematology
Published: July 06, 2023
Response to Prolonged Duration of Therapeutic Dose Oral Iron Therapy in a Girl With Novel TMPRSS6 Gene Variants: A Case Report and Review Literature.
Journal: Journal of pediatric hematology/oncology
Published: March 28, 2022
Whole-exome sequencing uncovered genetic diagnosis of severe inherited haemolytic anaemia: Correlation with clinical phenotypes.
Journal: British journal of haematology
Published: March 07, 2022
Corrigendum to: A Simple and Applicable Method for Human Platelet Lysate Preparation Using Citrate Blood.
Journal: Laboratory medicine
Published: February 14, 2022
A Simple and Applicable Method for Human Platelet Lysate Preparation Using Citrate Blood.
Journal: Laboratory medicine
Published: January 11, 2022
The use of immature platelet fraction to predict time to platelet recovery in patients with dengue infection.
Journal: Paediatrics and international child health
Published: December 07, 2019
Reticulocyte hemoglobin equivalent in a thalassemia-prevalent area.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: June 20, 2018
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Last Updated: 09/26/2026