Sakorn Pornprasert

10PUBLICATIONS
3CO-AUTHORS
Cardiovascular medicine and haematology not elsewhere classifiedHaematologyEpigenetics (incl. genome methylation and epigenomics)Genetics not elsewhere classifiedNgā pūtaiao koiora-hauora, haumanu hoki o te Māori (Māori biomedical and clinical sciences)
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Publications (10)

|Apr 27, 2026
Compound Heterozygosity for Hb Queens Park (α32(B13)Met→Lys) and α-thalassemia Found in Northern Thailand.

|Jul 21, 2025
Alpha-Thalassemia Caused by ααIVSI-1(AGGT> AGAT) (HBA1: c.95 + 1G > A) Mutation and its Combinations with Other Forms of Thalassemia or Hemoglobinopathy in Northern Thailand.

Sakorn Pornprasert, Chedtapak Ruengdit, Manoo Punyamung

|May 06, 2025
Characterization of HbH Disease Caused by Compound Heterozygotes α+-Thalassemia 3.7 kb Deletion and a Large Novel α0-Thalassemia Deletion.

Chedtapak Ruengdit, Manoo Punyamung, Kritsanee Maneewong

|Aug 23, 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.

Duantida Songdej, Praguywan Kadegasem, Nongnuch Sirachainan

|Nov 06, 2023
Single-tube multiplex real-time PCR with EvaGreen and high-resolution melting analysis for diagnosis of α0-thalassemia--SEA,--THAI, and--CR type deletions.

Chedtapak Ruengdit, Manoo Punyamung, Nutjeera Intasai

|Sep 18, 2023
Identification of a novel and rare α0 -thalassemia 27.0 kb deletion with 9 bp insertion (Lamphun deletion; --LAMPHUN ) in a Thai family.

Pinyaphat Khamphikham, Wanicha Tepakhan, Siripong Tongjai

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Frequent Collaborators

2 joint publications

Pinyaphat Khamphikham

1 joint publications

Siripong Tongjai

1 joint publications

Nongnuch Sirachainan