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Transfusion|August 20, 2022
Red blood cell alloimmunization and other transfusion-related complications in patients with transfusion-dependent thalassemia: A multi-center study in ThailandNattiya Teawtrakul, Duantida Songdej, Chattree Hantaweepant, et al.
Pediatric Blood & Cancer|July 24, 2023
Thalassemia-related complications in pediatric, adolescent, and young adult patients with transfusion-dependent thalassemia: A multicenter study in ThailandPacharapan Surapolchai, Duantida Songdej, Chattree Hantaweepant, et al.
Asian Pacific Journal of Cancer Prevention : APJCP|September 29, 2022
KRAS Mutation in Pediatric Intracranial Germ Cell TumorsChusana Khaiman, Piti Techavichit, Hansamon Poparn, et al.
Annals of Hematology|November 23, 2023
Molecular characteristics of hereditary red blood cell membrane disorders in Thailand: a multi-center registryDuantida Songdej, Pacharapan Surapolchai, Patcharee Komwilaisak, et al.
Clinical and Experimental Pediatrics|March 13, 2026
Outcomes of hematopoietic stem cell transplantation for pediatric patients with transfusion-dependent thalassemia in ThailandKleebsabai Sanpakit, Kamala Laohverapanich, Bunchoo Pongtanakul, et al.
British Journal of Haematology|October 31, 2024
Impact of HbE mutation on the clinical severity of HbH disease: A multicentre study from ThailandDuantida Songdej, Nattiya Teawtrakul, Napat Laoaroon, et al.
Scientific Reports|June 13, 2026
Disease-related complications and risk factors in hemoglobin H disease in a Thai multicenter registryNattiya Teawtrakul, Duantida Songdej, Chattree Hantaweepant, et al.
Journal of Medical Genetics|October 18, 2018
Biallelic mutations in EXOC3L2 cause a novel syndrome that affects the brain, kidney and bloodAdel Shalata, Supanun Lauhasurayotin, Zvi Leibovitz, et al.
NPJ Genomic Medicine|December 17, 2019
Reanalysing genomic data by normalized coverage values uncovers CNVs in bone marrow failure gene panelsSupanun Lauhasurayotin, Geoff D Cuvelier, Robert J Klaassen, et al.
British Journal of Haematology|March 5, 2020
Androgen therapy in inherited bone marrow failure syndromes: analysis from the Canadian Inherited Marrow Failure RegistryAlbert Català, Salah S Ali, Geoffrey D E Cuvelier, et al.
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