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Journal Articles

The Unusual Pathobiology of Hemoglobin Constant Spring Red Blood Cells

S.L. Schrier, A. Bunyaratvej, A. Khuhapinant, S. Fucharoen, M. Aljurf, L.M. Snyder, C.R. Keifer, L. Ma, N. Mohandas

Blood (1997) 89 (5): 1762–1769.

https://doi.org/10.1182/blood.V89.5.1762

Published: 1997

Journal Articles

Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in beta-thalassemia/hemoglobin E disease

S Fucharoen, N Siritanaratkul, P Winichagoon, J Chowthaworn, W Siriboon, W Muangsup, S Chaicharoen, N Poolsup, B Chindavijak, P Pootrakul, A Piankijagum, AN Schechter, GP Rodgers

Blood (1996) 87 (3): 887–892.

https://doi.org/10.1182/blood.V87.3.887.bloodjournal873887

Published: 1996

Journal Articles

The instability of the membrane skeleton in thalassemic red blood cells

J Yuan, A Bunyaratvej, S Fucharoen, C Fung, E Shinar, SL Schrier

Blood (1995) 86 (10): 3945–3950.

https://doi.org/10.1182/blood.V86.10.3945.bloodjournal86103945

Published: 1995

Journal Articles

Reduced deformability of thalassemic erythrocytes and erythrocytes with abnormal hemoglobins and relation with susceptibility to Plasmodium falciparum invasion

A Bunyaratvej, P Butthep, N Sae-Ung, S Fucharoen, Y Yuthavong

Blood (1992) 79 (9): 2460–2463.

https://doi.org/10.1182/blood.V79.9.2460.2460

Published: 1992

Journal Articles

Asymmetrically primed selective amplification/temperature shift fluorescence polymerase chain reaction to detect the hemoglobin Constant Spring mutation

GL Kropp, S Fucharoen, SH Embury

Blood (1991) 78 (1): 26–29.

https://doi.org/10.1182/blood.V78.1.26.26

Published: 1991

Journal Articles

Three-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta gunma) with a thalassemia-like phenotype [letter]

S Fucharoen, G Fucharoen, Y Fukumaki, Y Nakayama, Y Hattori, K Yamamoto, Y Ohba

Blood (1990) 76 (9): 1894–1896.

https://doi.org/10.1182/blood.V76.9.1894.1894

Published: 1990

Journal Articles

Selective enzymatic amplification of alpha 2-globin DNA for detection of the hemoglobin Constant Spring mutation

GL Kropp, S Fucharoen, SH Embury

Blood (1989) 73 (7): 1987–1992.

https://doi.org/10.1182/blood.V73.7.1987.1987

Published: 1989

Journal Articles

The effect of erythroid hyperplasia on iron balance

P Pootrakul, K Kitcharoen, P Yansukon, P Wasi, S Fucharoen, P Charoenlarp, G Brittenham, MJ Pippard, CA Finch

Blood (1988) 71 (4): 1124–1129.

https://doi.org/10.1182/blood.V71.4.1124.1124

Published: 1988

NARROW

The Unusual Pathobiology of Hemoglobin Constant Spring Red Blood Cells

Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in beta-thalassemia/hemoglobin E disease

The instability of the membrane skeleton in thalassemic red blood cells

Reduced deformability of thalassemic erythrocytes and erythrocytes with abnormal hemoglobins and relation with susceptibility to Plasmodium falciparum invasion

Asymmetrically primed selective amplification/temperature shift fluorescence polymerase chain reaction to detect the hemoglobin Constant Spring mutation

Three-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta gunma) with a thalassemia-like phenotype [letter]

Selective enzymatic amplification of alpha 2-globin DNA for detection of the hemoglobin Constant Spring mutation

The effect of erythroid hyperplasia on iron balance

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American Society of Hematology

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ASH Publications

American Society of Hematology

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