Search Results - "Wasi, Prawase"

Quantitative study of erythrocyte glucose-6-phosphate dehydrogenase by Vicharn Panich, Prawase Wasi

“…The method and result of erythrocyte glucose-6-phosphate dehydrogenase (G6PD) assay in Thai subjects are presented. In 266 males the distribution of G6PD…”
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Genetic factors affecting clinical severity in beta-thalassemia syndromes by Winichagoon, P, Fucharoen, S, Chen, P, Wasi, P

“…Heterogeneity in the clinical manifestation of beta-thalassemic diseases may occur from the nature of beta-globin gene mutations, alpha-thalassemia gene…”
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A correlation of erythrokinetics, ineffective erythropoiesis, and erythroid precursor apoptosis in Thai patients with thalassemia by Pootrakul, Pensri, Sirankapracha, Pornpan, Hemsorach, Surai, Moungsub, Wanna, Kumbunlue, Rawiprapa, Piangitjagum, Anong, Wasi, Prawase, Ma, Lisa, Schrier, Stanley L.

“…The variety of patients with thalassemia in Thailand offers an opportunity to fully characterize the kinetic causes of the anemia and to study apoptosis of…”
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A correlation of erythrokinetics, ineffective erythropoiesis, and erythroid precursor apoptosis in Thai patients with thalassemia by Pootrakul, Pensri, Sirankapracha, Pornpan, Hemsorach, Surai, Moungsub, Wanna, Kumbunlue, Rawiprapa, Piangitjagum, Anong, Wasi, Prawase, Ma, Lisa, Schrier, Stanley L.

“…The variety of patients with thalassemia in Thailand offers an opportunity to fully characterize the kinetic causes of the anemia and to study apoptosis of…”
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Acute hemolysis in glucose-6-phosphate dehydrogenase deficiency a study in 20 patients by Supa Na-Nakorn, Prawase Wasi, Vicharn Panich, Munsit Sookanek, Malida Pornpatkut, Pensri Pootrakul

“…All patients were male 13 to 53 years old. 19 of them had fever; acute hemolysis occurred 2-3 or more days after administration of drugs in 15, and 4 had acute…”
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Clinical manifestation of beta-thalassemia/hemoglobin E disease by Fucharoen, S, Ketvichit, P, Pootrakul, P, Siritanaratkul, N, Piankijagum, A, Wasi, P

“…To review the clinical manifestation and changes in hematologic parameters of patients with beta-thalassemia/hemoglobin (Hb) E. Retrospective analysis of the…”
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Increased red blood cell protoporphyrin in thalassemia: a result of relative iron deficiency by Pootrakul, P, Wattanasaree, J, Anuwatanakulchai, M, Wasi, P

“…Erythrocyte protoporphyrin (EP) was measured in 50 normal control subjects, 22 iron-responsive anemic subjects, and in 106 patients with thalassemic diseases…”
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Quantitative changes of red blood cell shapes in relation to clinical features in beta-thalassemia/HbE disease by Bunyaratvej, A, Sahaphong, S, Bhamarapravati, N, Wasi, P

“…Quantitative analysis of red blood cell (RBC) shapes was performed in 79 patients with beta-thalassemia/HbE disease, using scanning electron microscopy (SEM)…”
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Increased phagocytosis of Plasmodium falciparum-infected erythrocytes with haemoglobin E by peripheral blood monocytes by Bunyaratvej, A, Butthep, P, Yuthavong, Y, Fucharoen, S, Khusmith, S, Yoksan, S, Wasi, P

“…Erythrocytes from subjects with homozygous and heterozygous haemoglobin E (HbE) infected with Plasmodium falciparum in vitro were phagocytosed to a greater…”
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Severity differences in beta-thalassaemia/haemoglobin E syndromes: implication of genetic factors by Winichagoon, P, Thonglairoam, V, Fucharoen, S, Wilairat, P, Fukumaki, Y, Wasi, P

“…Genetic factors determining the difference in severity of anaemia in beta-thalassaemia/HbE disease were studied in 90 patients who had haemoglobin levels, at…”
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Determination for different severity of anemia in thalassemia: concordance and discordance among sib pairs by Fucharoen, S, Winichagoon, P, Pootrakul, P, Wasi, P

“…The degree of anemia in beta(0)-thalassemia/hemoglobin E disease is highly variable. As part of an attempt to identify determinants of this variability of…”
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Presence of immunoglobulins, C3 and cytolytic C5b‐9 complement components on the surface of erythrocytes from patients with β‐thalassaemia/HbE disease by Malasit, Prida, Mahasorn, Weerawuth, Mongkolsapaya, Juthathip, Singhathong, Benjawan, Fucharoen, Suthat, Wasi, Prawase, Bhakdi, Sucharit

“…The occurrence of IgG, IgM, IgA, C3 and C5b‐9 complement complexes on erythrocytes from 43 patients with β‐thalassaemia HbE disease was investigated. Indirect…”
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The Effect of Erythroid Hyperplasia on Iron Balance by Pootrakul, Pensri, Kitcharoen, Kriengkrai, Yansukon, Pornpan, Wasi, Prawase, Fucharoen, Suthat, Charoenlarp, Preecha, Brittenham, Gary, Pippard, Martin J., Finch, Clement A.

“…Measurements of erythropoiesis and iron balance were made in eight normal and 32 anemic subjects. The latter consisted of 12 individuals with ineffective…”
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Beta-thalassemia in Thailand by Winichagoon, P, Fucharoen, S, Thonglairoam, V, Tanapotiwirut, V, Wasi, P

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Thalassaemia Genes by Wasi, Prawase

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Thalassemia genes by Wasi, P

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Thalassemia in southeast Asia: determination of different degrees of severity of anemia in thalassemia by Wasi, P, Pootrakul, P, Fucharoen, S, Winichagoon, P, Wilairat, P, Promboon, A

“…beta (0)-Thalassemia/Hb E in Southeast Asia varies greatly in severity, with hemoglobin levels ranging from 2.5 to 13.5 g/dl, averaging 7.7 g/dl. Results of…”
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Intracranial extramedullary hematopoiesis in beta-thalassemia/hemoglobin E disease by Fucharoen, S, Tunthanavatana, C, Sonakul, D, Wasi, P

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Cardiac pathology in 47 patients with beta thalassaemia/haemoglobin E by Sonakul, D, Pacharee, P, Wasi, P, Fucharoen, S

“…Autopsy protocols and heart slides of 47 patients with beta thalassaemia/haemoglobin E disease were reviewed. All but 1 patient had cardiac hypertrophy,…”
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Brief Note: Hemoglobin J in an American Caucasian Family of Swedish Ancestry by WASI, PRAWASE, GITHENS, JOHN, HATHAWAY, WILLIAM

“…Two instances of the heterozygous state of hemoglobin J are described in the male members of an American Caucasian family of Swedish ancestry…”
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