List of works - Pimlak Charoenkwan

A Longitudinal Study of Growth and Relation With Anemia and Iron Overload in Pediatric Patients With Transfusion-dependent Thalassemia

scientific article published in August 2016

A Randomized, Open-Labeled, Prospective Controlled Study to Assess the Efficacy of Frontline Empirical Intravenous Piperacillin/Tazobactam Monotherapy in Comparison with Ceftazidime Plus Amikacin for Febrile Neutropenia in Pediatric Oncology Patient

scientific article published on 01 September 2019

Acute Non-Atherosclerotic ST-Segment Elevation Myocardial Infarction in an Adolescent with Concurrent Hemoglobin H-Constant Spring Disease and Polycythemia Vera.

scientific article published on 23 September 2015

Adverse effects of imatinib in children with chronic myelogenous leukemia

scientific article published on 19 August 2016

Anemia and hydrops in a fetus with homozygous hemoglobin constant spring

scientific article published on 01 December 2006

Borderline hemoglobin A levels in northern Thai population: HBB genotypes and effects of coinherited alpha-thalassemia

scientific article published on 04 October 2018

Calreticulin mutation analysis in non-mutated Janus kinase 2 essential thrombocythemia patients in Chiang Mai University: analysis of three methods and clinical correlations

scientific article published on 9 March 2018

Cardiorenal syndrome in thalassemia patients

scientific article published on 03 August 2020

Coinheritance of Hereditary Elliptocytosis and Deletional Hemoglobin H Disease

scientific article published on 5 January 2017

Compound heterozygosity of a silent beta-thalassemia mutation at the 3'-untranslated region (HBB: c.*132 C>T) and beta-zero thalassemia results in thalassemia intermedia

scientific article published on 13 January 2020

Cord blood screening for alpha-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: correlation with genotypes and hematologic parameters.

scientific article published on 17 March 2010

DeepThal: A Deep Learning-Based Framework for the Large-Scale Prediction of the α+-Thalassemia Trait Using Red Blood Cell Parameters

scientific article published in 2022

Discrepancy in the degree of polycythemia in a family with a novel nonsense EPOR mutation

scientific article published on 26 July 2019

Effectiveness of the model for prenatal control of severe thalassemia

scientific article published on 31 March 2013

FLT3, a prognostic biomarker for acute myeloid leukemia (AML): Quantitative monitoring with a simple anti-FLT3 interaction and flow cytometric method

scientific article published on 08 February 2019

Fetal anaemia from red blood cell membrane defect and co-inherited haemoglobin Constant Spring

scientific article published on 27 July 2015

Flow Cytometric Test with Eosin-5-Maleimide for a Diagnosis of Hereditary Spherocytosis in a Newborn

scientific article published on 07 May 2019

Genotypes and phenotypes of protein S deficiency in Thai children with thromboembolism.

scientific article published on 17 October 2016

Gingival Bleeding and Bloody Dialysate: A Case Report of Scurvy in a Child With End-Stage Renal Disease Receiving Peritoneal Dialysis

scientific article published on 23 April 2016

Hb H hydrops foetalis syndrome: a case report and review of literature.

scientific article

Health-Related Quality of Life in Adolescents with Thalassemia.

scientific article published on 18 June 2015

Heart Rate Variability as an Alternative Indicator for Identifying Cardiac Iron Status in Non-Transfusion Dependent Thalassemia Patients

scientific article published on 17 June 2015

Heart Rate Variability for Early Detection of Cardiac Iron Deposition in Patients with Transfusion-Dependent Thalassemia

scientific article

Heart rate variability in beta-thalassemia patients

scientific article published on 06 July 2009

Hematopoietic stem cell transplantation for homozygous β-thalassemia and β-thalassemia/hemoglobin E patients from haploidentical donors.

scientific article published on 15 February 2016

Hemodynamic assessment of hydrops foetalis secondary to transient myeloproliferative disorder associated with foetal Down syndrome: A case report and literature review

scientific article published on 9 September 2016

High-resolution melting analysis for prenatal diagnosis of beta-thalassemia in northern Thailand.

scientific article published on 8 August 2017

Hyperuricemia, urine uric excretion, and associated complications in thalassemia patients

scientific article published on 05 February 2019

Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII.

scientific article published on June 2006

Iron overload in non-transfusion-dependent thalassemia: association with genotype and clinical risk factors.

scientific article published on 6 April 2016

MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis.

scholarly article

Mass spectrometry-based detection of hemoglobin E mutation by allele-specific base extension reaction

scientific article published on 19 October 2007

Molecular and clinical features of Hb H disease in northern Thailand.

scientific article published in January 2005

Molecular characteristics of thalassemia and hemoglobin variants in prenatal diagnosis program in northern Thailand

scientific article published on 25 June 2019

No evidence of hemostasis disturbance in Thai children with iron deficiency anemia.

scientific article published on 9 September 2012

Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia

scientific article published on 10 September 2018

Outcomes of thalassemia patients undergoing hematopoietic stem cell transplantation by using a standard myeloablative versus a novel reduced-toxicity conditioning regimen according to a new risk stratification

scientific article published on 23 July 2014

Prenatal diagnosis and management of homozygous hemoglobin constant spring disease

scientific article published on 16 May 2019

Prenatal diagnosis of homozygous alpha-thalassemia-1 by cell-free fetal DNA in maternal plasma.

scientific article

Prevalence and Risk Factors for Complications in Patients with Nontransfusion Dependent Alpha- and Beta-Thalassemia.

scientific article

Prophylaxis in congenital factor VII deficiency: indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER).

scientific article published on 12 February 2013

Pulmonary hypertension in non-transfusion-dependent thalassemia: Correlation with clinical parameters, liver iron concentration, and non-transferrin-bound iron

scientific article published on 12 May 2015

Quantification of glucose-6-phosphate dehydrogenase activity by spectrophotometry: A systematic review and meta-analysis

scientific article published on 14 May 2020

R147W in PROC Gene Is a Risk Factor of Thromboembolism in Thai Children.

scientific article published in January 2017

Replacement therapy in inherited factor VII deficiency: occurrence of adverse events and relation with surgery

scientific article

Root dentin anomaly and a PLG mutation

scientific article published on 30 September 2014

Secondary erythrocytosis caused by hemoglobin Tak/β0-thalassaemia disease during pregnancy: A case report.

scientific article published on 14 December 2016

Significance of p53 expression in immature teratomas

scientific article published on 04 September 2002

Skin involvement in a newborn with down syndrome and transient myeloproliferative disorder

scientific article published on 01 May 2012

Successful treatment of mild pediatric kasabach-merritt phenomenon with propranolol monotherapy

scientific article

The association between pre-transfusion hemoglobin levels and thalassemia complications

scientific article published on 01 December 2021

The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.

scientific article published on 19 September 2014

The effect of polymorphisms of MTHFR C677T, A1298C, MS A2756G and CBS 844ins68bp on plasma total homocysteine level and the risk of ischemic stroke in Thai children.

scientific article published on 8 November 2007

Tissue Doppler echocardiography reliably reflects severity of iron overload in pediatric patients with beta thalassemia

scientific article published on 07 August 2007

Unusual Presentation with Orbital Mass in a Child with Precursor B-Cell Acute Lymphoblastic Leukemia

scientific article published on 05 November 2019

Use of cardiac markers for monitoring of doxorubixin-induced cardiotoxicity in children with cancer.

scientific article published in November 2012

Vincristine-induced polyneuropathy in a child with stage I Wilms' tumour presenting with unilateral abducens nerve palsy.

scientific article

Vitamin D deficiency and its relationship with cardiac iron and function in patients with transfusion-dependent thalassemia at Chiang Mai University Hospital.

scientific article published on 23 January 2018

List of works by Pimlak Charoenkwan

A Longitudinal Study of Growth and Relation With Anemia and Iron Overload in Pediatric Patients With Transfusion-dependent Thalassemia

A Randomized, Open-Labeled, Prospective Controlled Study to Assess the Efficacy of Frontline Empirical Intravenous Piperacillin/Tazobactam Monotherapy in Comparison with Ceftazidime Plus Amikacin for Febrile Neutropenia in Pediatric Oncology Patient

Acute Non-Atherosclerotic ST-Segment Elevation Myocardial Infarction in an Adolescent with Concurrent Hemoglobin H-Constant Spring Disease and Polycythemia Vera.

Adverse effects of imatinib in children with chronic myelogenous leukemia

Anemia and hydrops in a fetus with homozygous hemoglobin constant spring

Borderline hemoglobin A levels in northern Thai population: HBB genotypes and effects of coinherited alpha-thalassemia

Calreticulin mutation analysis in non-mutated Janus kinase 2 essential thrombocythemia patients in Chiang Mai University: analysis of three methods and clinical correlations

Cardiorenal syndrome in thalassemia patients

Coinheritance of Hereditary Elliptocytosis and Deletional Hemoglobin H Disease

Compound heterozygosity of a silent beta-thalassemia mutation at the 3'-untranslated region (HBB: c.*132 C>T) and beta-zero thalassemia results in thalassemia intermedia

Cord blood screening for alpha-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: correlation with genotypes and hematologic parameters.

DeepThal: A Deep Learning-Based Framework for the Large-Scale Prediction of the α+-Thalassemia Trait Using Red Blood Cell Parameters

Discrepancy in the degree of polycythemia in a family with a novel nonsense EPOR mutation

Effectiveness of the model for prenatal control of severe thalassemia

FLT3, a prognostic biomarker for acute myeloid leukemia (AML): Quantitative monitoring with a simple anti-FLT3 interaction and flow cytometric method

Fetal anaemia from red blood cell membrane defect and co-inherited haemoglobin Constant Spring

Flow Cytometric Test with Eosin-5-Maleimide for a Diagnosis of Hereditary Spherocytosis in a Newborn

Genotypes and phenotypes of protein S deficiency in Thai children with thromboembolism.

Gingival Bleeding and Bloody Dialysate: A Case Report of Scurvy in a Child With End-Stage Renal Disease Receiving Peritoneal Dialysis

Hb H hydrops foetalis syndrome: a case report and review of literature.

Health-Related Quality of Life in Adolescents with Thalassemia.

Heart Rate Variability as an Alternative Indicator for Identifying Cardiac Iron Status in Non-Transfusion Dependent Thalassemia Patients

Heart Rate Variability for Early Detection of Cardiac Iron Deposition in Patients with Transfusion-Dependent Thalassemia

Heart rate variability in beta-thalassemia patients

Hematopoietic stem cell transplantation for homozygous β-thalassemia and β-thalassemia/hemoglobin E patients from haploidentical donors.

Hemodynamic assessment of hydrops foetalis secondary to transient myeloproliferative disorder associated with foetal Down syndrome: A case report and literature review

High-resolution melting analysis for prenatal diagnosis of beta-thalassemia in northern Thailand.

Hyperuricemia, urine uric excretion, and associated complications in thalassemia patients

Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII.

Iron overload in non-transfusion-dependent thalassemia: association with genotype and clinical risk factors.

MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis.

Mass spectrometry-based detection of hemoglobin E mutation by allele-specific base extension reaction

Molecular and clinical features of Hb H disease in northern Thailand.

Molecular characteristics of thalassemia and hemoglobin variants in prenatal diagnosis program in northern Thailand

No evidence of hemostasis disturbance in Thai children with iron deficiency anemia.

Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia

Outcomes of thalassemia patients undergoing hematopoietic stem cell transplantation by using a standard myeloablative versus a novel reduced-toxicity conditioning regimen according to a new risk stratification

Prenatal diagnosis and management of homozygous hemoglobin constant spring disease

Prenatal diagnosis of homozygous alpha-thalassemia-1 by cell-free fetal DNA in maternal plasma.

Prevalence and Risk Factors for Complications in Patients with Nontransfusion Dependent Alpha- and Beta-Thalassemia.

Prophylaxis in congenital factor VII deficiency: indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER).

Pulmonary hypertension in non-transfusion-dependent thalassemia: Correlation with clinical parameters, liver iron concentration, and non-transferrin-bound iron

Quantification of glucose-6-phosphate dehydrogenase activity by spectrophotometry: A systematic review and meta-analysis

R147W in PROC Gene Is a Risk Factor of Thromboembolism in Thai Children.

Replacement therapy in inherited factor VII deficiency: occurrence of adverse events and relation with surgery

Root dentin anomaly and a PLG mutation

Secondary erythrocytosis caused by hemoglobin Tak/β0-thalassaemia disease during pregnancy: A case report.

Significance of p53 expression in immature teratomas

Skin involvement in a newborn with down syndrome and transient myeloproliferative disorder

Successful treatment of mild pediatric kasabach-merritt phenomenon with propranolol monotherapy

The association between pre-transfusion hemoglobin levels and thalassemia complications

The correlation of α-globin gene mutations and the XmnI polymorphism with clinical severity of Hb E/β-thalassemia.

The effect of polymorphisms of MTHFR C677T, A1298C, MS A2756G and CBS 844ins68bp on plasma total homocysteine level and the risk of ischemic stroke in Thai children.

Tissue Doppler echocardiography reliably reflects severity of iron overload in pediatric patients with beta thalassemia

Unusual Presentation with Orbital Mass in a Child with Precursor B-Cell Acute Lymphoblastic Leukemia

Use of cardiac markers for monitoring of doxorubixin-induced cardiotoxicity in children with cancer.

Vincristine-induced polyneuropathy in a child with stage I Wilms' tumour presenting with unilateral abducens nerve palsy.

Vitamin D deficiency and its relationship with cardiac iron and function in patients with transfusion-dependent thalassemia at Chiang Mai University Hospital.