Clinical paroxysmal nocturnal hemoglobinuria is the result of expansion of glycosyl-phosphatidyl-inositol-anchored protein-deficient clone in the condition of deficient hematopoies...

by Kriangsak Pakdeesuwan
Published 2018

Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals

by David J. Araten, Khedoudja Nafa, Kriangsak Pakdeesuwan, Lucio Luzzatto
Published 2018

Immunophenotypic discrepancies between granulocytic and erythroid lineages in peripheral blood of patients with paroxysmal nocturnal haemoglobinuria

by Kriangsak Pakdeesuwan, Wanchai Wanachiwanawin, Uamporn Siripanyaphinyo, Kovit Pattanapanyasat, Prapon Wilairat, Surapol Issaragrisil
Published 2018

Genotypic and phenotypic implications in paroxysmal nocturnal hemoglobinuria (PNH): A preliminary investigation

by Kriangsak Pakdeesuwan, Uamporn Siripanyaphinyo, Patcharin Pramoonjago, Kovit Pattanapanyasat, Prapon Wilairat, Taroh Kinoshita, Wanchai Wanachiwanawin
Published 2018