The first validated criteria for effective screening and a new simplified method for α-globin gene sequencing for diagnosis of uncommon α-globin mutations
Uaprasert, Noppacharn, Settapiboon, Rung, Amornsiriwat, Supaporn, Sutcharitchan, Pranee, Rojnuckarin, Ponlapat
Published in International journal of hematology (01.06.2017)
Published in International journal of hematology (01.06.2017)
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Journal Article
Hemoglobin h disease classification by isoelectric focusing : Molecular verification of 110 cases from thailand
SUTCHARITCHAN, Pranee, WEN WANG, SETTAPIBOON, Rung, AMORNSIRIWAT, Supaporn, TAN, Arnold S. C, CHONG, Samuel S
Published in Clinical chemistry (Baltimore, Md.) (01.03.2005)
Published in Clinical chemistry (Baltimore, Md.) (01.03.2005)
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Journal Article
Good Prognosis of Adult Hemophagocytic Lymphohistiocytosis (HLH) Associated with the HAVCR2 germline Mutation
Boonyabaramee, Pitchayut, Polprasert, Chantana, Kongkiatkamon, Sunisa, Kobbuaklee, Sirorat, Settapiboon, Rung, Pongudom, Saranya, Faknuam, Saruta, Rojnuckarin, Ponlapat
Published in Blood (15.11.2022)
Published in Blood (15.11.2022)
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Journal Article
Good prognosis of adult hemophagocytic lymphohistiocytosis associated with the germline HAVCR2 mutation
Boonyabaramee, Pitchayut, Polprasert, Chantana, Kobbuaklee, Sirorat, Settapiboon, Rung, Pongudom, Saranya, Faknuam, Saruta, Kongkiatkamon, Sunisa, Wudhikarn, Kitsada, Rojnuckarin, Ponlapat
Published in Experimental hematology (01.09.2023)
Published in Experimental hematology (01.09.2023)
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Journal Article
Stability of Hemoglobin Constant Spring Identified by Capillary Electrophoresis
Jaitheang, Jidapa, Suksusut, Amornchai, Settapiboon, Rung, Amornsiriwat, Supaporn, Sutcharitchan, Pranee, Uaprasert, Noppacharn, Rojnuckarin, Ponlapat
Published in Laboratory medicine (02.05.2023)
Published in Laboratory medicine (02.05.2023)
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Journal Article
An Effective Screening Algorithm and a Simple DNA Sequencing Protocol for Molecular Characterization of Rare Alpha-Globin Variants
Uaprasert, Noppacharn, Settapiboon, Rung, Amornsiriwat, Supaporn, Sutcharitchan, Pranee, Rojnuckarin, Ponlapat
Published in Blood (03.12.2015)
Published in Blood (03.12.2015)
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Journal Article
The first validated criteria for effective screening and a new simplified method for [alpha]-globin gene sequencing for diagnosis of uncommon [alpha]-globin mutations
Uaprasert, Noppacharn, Settapiboon, Rung, Amornsiriwat, Supaporn, Sutcharitchan, Pranee, Rojnuckarin, Ponlapat
Published in International journal of hematology (01.06.2017)
Published in International journal of hematology (01.06.2017)
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Journal Article
Comprehensive screening for coexisting heterozygous α 0 -thalassemia in hemoglobin E trait
Polprasert, Chantana, Wongprachar, Piroonrut, Suksusut, Amornchai, Settapiboon, Rung, Amornsirivat, Supaporn, Sophonphan, Jiratchaya, Uaprasert, Noppacharn, Sucharitchan, Pranee, Rojnuckarin, Ponlapat
Published in Hematology (Luxembourg) (01.12.2020)
Published in Hematology (Luxembourg) (01.12.2020)
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Journal Article
Diagnostic utility of isoelectric focusing and high performance liquid chromatography in neonatal cord blood screening for thalassemia and non-sickling hemoglobinopathies
Uaprasert, Noppacharn, Settapiboon, Rung, Amornsiriwat, Supaporn, Sarnthammakul, Patsita, Thanapat, Tassanee, Rojnuckarin, Ponlapat, Sutcharitchan, Pranee
Published in Clinica chimica acta (01.01.2014)
Published in Clinica chimica acta (01.01.2014)
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Journal Article
Comprehensive screening for coexisting heterozygous α0-thalassemia in hemoglobin E trait
Polprasert, Chantana, Wongprachar, Piroonrut, Suksusut, Amornchai, Settapiboon, Rung, Amornsirivat, Supaporn, Sophonphan, Jiratchaya, Uaprasert, Noppacharn, Sucharitchan, Pranee, Rojnuckarin, Ponlapat
Published in Hematology (Luxembourg) (01.12.2020)
Published in Hematology (Luxembourg) (01.12.2020)
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Journal Article
Hematological characteristics and effective screening for compound heterozygosity for Hb constant spring and deletional α+‐thalassemia
Uaprasert, Noppacharn, Rojnuckarin, Ponlapat, Settapiboon, Rung, Amornsiriwat, Supaporn, Sutcharitchan, Pranee
Published in American journal of hematology (01.07.2011)
Published in American journal of hematology (01.07.2011)
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Journal Article
Diagnostic Utility of Isoelectric Focusing and High Performance Liquid Chromatography in Fetal Cord Blood Screening for Thalassemia and Non-Sickling Hemoglobinopathies
Uaprasert, Noppacharn, Settapiboon, Rung, Amornsiriwat, Supaporn, Sarnthammakul, Patsita, Rojnuckarin, Ponlapat, Sutcharitchan, Pranee
Published in Blood (18.11.2011)
Published in Blood (18.11.2011)
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Journal Article
Hematological characteristics and effective screening for compound heterozygosity for Hb constant spring and deletional [alpha]+-thalassemia
Uaprasert, Noppacharn, Rojnuckarin, Ponlapat, Settapiboon, Rung, Amornsiriwat, Supaporn, Sutcharitchan, Pranee
Published in American journal of hematology (01.07.2011)
Published in American journal of hematology (01.07.2011)
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Journal Article
Elevated serum transferrin receptor levels in common types of thalassemia heterozygotes in Southeast Asia: A correlation with genotypes and red cell indices
Uaprasert, Noppacharn, Rojnuckarin, Ponlapat, Bhokaisawan, Narudee, Settapiboon, Rung, Wacharaprechanont, Teera, Amornsiriwat, Siriporn, Sutcharitchan, Pranee
Published in Clinica chimica acta (01.05.2009)
Published in Clinica chimica acta (01.05.2009)
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Journal Article
Severe β0 thalassemia/hemoglobin E disease caused by de novo 22‐base pair duplication in the paternal allele of β globin gene
Rojnuckarin, Ponlapat, Settapiboon, Rung, Vanichsetakul, Preeda, Sueblinvong, Tada, Sutcharitchan, Pranee
Published in American journal of hematology (01.07.2007)
Published in American journal of hematology (01.07.2007)
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Journal Article
Severe phi 0 thalassemia/hemoglobin E disease caused by de novo 22-base pair duplication in the paternal allele of phi globin gene
Rojnuckarin, Ponlapat, Settapiboon, Rung, Vanichsetakul, Preeda, Sueblinvong, Tada, Sutcharitchan, Pranee
Published in American journal of hematology (01.07.2007)
Published in American journal of hematology (01.07.2007)
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Journal Article
Severe β 0 thalassemia/hemoglobin E disease caused by de novo 22‐base pair duplication in the paternal allele of β globin gene
Rojnuckarin, Ponlapat, Settapiboon, Rung, Vanichsetakul, Preeda, Sueblinvong, Tada, Sutcharitchan, Pranee
Published in American journal of hematology (01.07.2007)
Published in American journal of hematology (01.07.2007)
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Journal Article
Severe beta(0) thalassemia/hemoglobin E disease caused by de novo 22-base pair duplication in the paternal allele of beta globin gene
Rojnuckarin, Ponlapat, Settapiboon, Rung, Vanichsetakul, Preeda, Sueblinvong, Tada, Sutcharitchan, Pranee
Published in American journal of hematology (01.07.2007)
Published in American journal of hematology (01.07.2007)
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Journal Article