INCREASED TRANSFERRIN IRON SATURATION IN SPLENECTOMIZED THALASSAEMIC PATIENTSPOOTRAKUL P; RUGKIATSAKUL R; WASI P et al.1980; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1980; VOL. 46; NO 1; PP. 143-145; BIBL. 14 REF.Article

IMMUNOLOGIC DIAGNOSIS OF ALPHA -THALASSEMIA TRAITSWASI P; PRAVATMUANG P; WINICHAGOON P et al.1979; HEMOGLOBIN; USA; DA. 1979; VOL. 3; NO 1; PP. 21-31; BIBL. 18 REF.Article

PAROXYSMAL NOCTURNAL HAEMOGLOBINURIA IN THAILAND WITH SPECIAL REFERENCE TO AN ASSOCIATION WITH APLASTIC ANAEMIAKRUATRACHUE M; WASI P; NA NAKORN S et al.1978; BRIT. J. HAEMATOL.; GBR; DA. 1978; VOL. 39; NO 2; PP. 267-276; BIBL. 18 REF.Article

HEMOGLOBIN CONSTANT SPRING: HEMOGLOBIN SYNTHESIS IN HETEROZYGOUS STATESPONGAMART S; POOTRAKUL S; WASI P et al.1975; BIOCHEM. BIOPHYS. RES. COMMUNIC.; U.S.A.; DA. 1975; VOL. 64; NO 2; PP. 681-686; BIBL. 21 REF.Article

SERUM FERRITIN LEVELS IN THALASSEMIAS AND THE EFFECT OF SPLENECTOMYPOOTRAKUL P; VONGSMASA V; LA ONGPANICH P et al.1981; ACTA HAEMATOL.; ISSN 0001-5792; CHE; DA. 1981; VOL. 66; NO 4; PP. 244-250; BIBL. 21 REF.Article

INEFFECTIVE ERYTHROPOIESIS IN HAEMOGLOBIN EBETA -THALASSAEMIA: AN ELECTRON MICROSCOPE STUDYWICKRAMASINGHE SN; HUGHES M; WASI P et al.1981; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1981; VOL. 48; NO 3; PP. 451-457; BIBL. 2 P.Article

SERUM ERYTHROCYTE FOLATE LEVELS IN THALASSAEMIC PATIENTS IN THAILANDVATANAVICHARN S; ANUVATANAKULCHAI M; NA NAKORN S et al.1979; SCAND. J. HAEMATOL.; DNK; DA. 1979; VOL. 22; NO 3; PP. 241-245; BIBL. 18 REF.Article

HAEMOGLOBIN BART'S HYDROPS SYNDROME IN GREECEKATTAMIS C; METAXOTOU MAVROMATI A; TSIARTIA E et al.1980; BRIT. MED. J.; GBR; DA. 1980; VOL. 281; NO 6235; PP. 268-270; BIBL. 14 REF.Article

Comparison of erythrocyte antioxidative enzyme activities between two types of haemoglobin H diseasePRASARTKAEW, S; BUNYARATVEJ, A; FUCHAROEN, S et al.Journal of clinical pathology. 1986, Vol 39, Num 12, pp 1299-1303, issn 0021-9746Article

The molecular basis of AE-Bart's diseaseTHONGLAIRUAM, V; WINICHAGOON, P; FUCHAROEN, S et al.Hemoglobin. 1989, Vol 13, Num 2, pp 117-124, issn 0363-0269Article

EF Bart's disease: interaction of the abnormal α- and β-globin genesFUCHAROEN, S; WINICHAGOON, P; THONGLAIRUAM, V et al.European journal of haematology. 1988, Vol 40, Num 1, pp 75-78, issn 0902-4441Article

ENDOCRINE FUNCTION IN THALASSAEMIAVANNASAENG S; PLOYBUTA S; VISUTKUL P et al.1981; CLIN. ENDOCRINOL. (OXF.); ISSN 0300-0664; GBR; DA. 1981; VOL. 14; NO 2; PP. 165-173; BIBL. 2 P.Article

A SYNDROME OF HYPERTENSION, CONVULSION, AND CEREBRAL HAEMORRHAGE IN THALASSAEMIC PATIENTS AFTER MULTIPLE BLOOD-TRANSFUSIONSWASI P; NA NAKORN S; POOTRAKUL P et al.1978; LANCET; GBR; DA. 1978; NO 8090; PP. 602-604; BIBL. 16 REF.Article

THAI Gγ(Aγδβ)°-Thalassemia and its interaction with a single γ-globin gene on a chromosome carrying β°-ThalassemiaWINICHAGOON, P; FUCHAROEN, S; THONGLAIROAM, V et al.Hemoglobin. 1990, Vol 14, Num 2, pp 185-197, issn 0363-0269, 13 p.Article

Different molecular defects of ^Gγ(^AγSβ)-thalassaemia in ThailandFUCHAROEN, S; WINICHAGOON, P; CHAICHAROEN, S et al.European journal of haematology. 1987, Vol 39, Num 2, pp 154-160, issn 0902-4441Article

Different severity of homozygous β-thalassemia among siblingsWINICHAGOON, P; FUCHAROEN, S; THONGLAIROAM, V et al.Human genetics. 1987, Vol 76, Num 3, pp 296-297, issn 0340-6717Article

Cord blood study on β-thalassemia and hemoglobin EPOOTRAKUL, S; MUANG-SUP, V; FUCHAROEN, S et al.American journal of medical genetics. 1988, Vol 29, Num 1, pp 49-57, issn 0148-7299Article

Failure of pulse high-dose dexamethasone in chronic idiopathic immune thrombocytopeniaWARNER, M; WASI, P; COUBAN, S et al.American journal of hematology. 1997, Vol 54, Num 4, pp 267-270, issn 0361-8609Article

Presence of immunoglobulins, C3 and cytolytic C5b-9 complement components on the surface of erythrocytes from patients with β-thalassaemia/HbE diseaseMALASIT, P; MAHASORN, W; MONGKOLSAPAYA, J et al.British journal of haematology. 1997, Vol 96, Num 3, pp 507-513, issn 0007-1048Article

Improved technic for detecting intraerythrocytic inclusion bodies in α Thalassemia traitHAUNGSAPAYA, W; WINICHAGOON, P; FUCHAROEN, S et al.Chot Mai Het Thang Phaet. 1985, Vol 68, Num 1, pp 43-45, issn 0125-2208Article

Bacterial infection-associated improvement of platelet counts in two patients with chronic and unresponsive idiopathic thrombocytopenic purpura with normal platelet survival studiesBORDIN, J. O; SMITH, J. W; HAYWARD, C. P. M et al.British journal of haematology. 1995, Vol 90, Num 2, pp 332-335, issn 0007-1048Article

The effect of erythroid hyperplasia on iron balancePOOTRAKUL, P; KITCHAROEN, K; YANSUKON, P et al.Blood. 1988, Vol 71, Num 4, pp 1124-1129, issn 0006-4971Article

Activation of monocytes for the immune clearance of red cells in β°-thalassaemia/HbEWANACHIWANAWIN, W; SIRIPANYAPHINYO, U; FUCHAROEN, S et al.British journal of haematology. 1993, Vol 85, Num 4, pp 773-777, issn 0007-1048Article

Hemoglobin constant spring in Bangkok : molecular screening by selective enzymatic amplification of the α₂-globin geneTHONGLAIROAM, V; WINICHAGOON, P; FUCHAROEN, S et al.American journal of hematology. 1991, Vol 38, Num 4, pp 277-280, issn 0361-8609Article

The molecular basis of β-thalassemia in Thailand : application to prenatal diagnosisTHEIN, S. L; WINICHAGOON, P; HESKETCH, C et al.American journal of human genetics. 1990, Vol 47, Num 3, pp 369-375, issn 0002-9297, 7 p.Article