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S Fucharoen

Showing results (121-130 of 254) with videos related to

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European Journal of Haematology|February 13, 2001
Clinical and hematological features of codon 17, A-T mutation of beta-thalassemia in Thai patientsV Laosombat, M Wongchanchailert, B Sattayasevana, et al.
British Journal of Haematology|August 1, 1994
Nondeletional type of hereditary persistence of fetal haemoglobin: molecular characterization of three unrelated Thai HPFHP Winichagoon, S Fucharoen, P Wilairat, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosisS Fucharoen, G Fucharoen, T Ratanasiri, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|December 1, 1980
Pulmonary artery obstruction in thalassaemiaD Sonakul, P Pacharee, T Laohapand, et al.
Birth Defects Original Article Series|January 1, 1987
Altered structure of spectrin in the two types of hemoglobin H diseaseP Lamchiagdhase, P Wilairat, A Bunyaratvej, et al.
Hemoglobin|March 18, 2000
Hb Siam [alpha15(A13)Gly-->Arg] is a GGT-->CGT mutation in the alpha1-globin geneB Yodsowan, J Svast, C Srisomsap, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|December 1, 1982
Heterogeneity of beta thalassaemia in ThailandP Yenchitsomanus, A Baramee, S Fucharoen, et al.
Clinical and Laboratory Haematology|October 16, 2004
Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in ThailandS Chunpanich, K Ayukarn, K Sanchaisuriya, et al.
Birth Defects Original Article Series|January 1, 1987
Alpha-mRNA level in the two types of Hb H diseaseP Winichagoon, W Chulalaksananukul, S Panyim, et al.
Acta Endocrinologica|January 1, 1991
Pituitary function in thalassemic patients and the effect of chelation therapyS Vannasaeng, S Fucharoen, P Pootrakul, et al.
Pageof 26

Showing results (121-130 of 254) with videos related to

Sort By:
Pageof 26
European Journal of Haematology|February 13, 2001
Clinical and hematological features of codon 17, A-T mutation of beta-thalassemia in Thai patientsV Laosombat, M Wongchanchailert, B Sattayasevana, et al.
British Journal of Haematology|August 1, 1994
Nondeletional type of hereditary persistence of fetal haemoglobin: molecular characterization of three unrelated Thai HPFHP Winichagoon, S Fucharoen, P Wilairat, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosisS Fucharoen, G Fucharoen, T Ratanasiri, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|December 1, 1980
Pulmonary artery obstruction in thalassaemiaD Sonakul, P Pacharee, T Laohapand, et al.
Birth Defects Original Article Series|January 1, 1987
Altered structure of spectrin in the two types of hemoglobin H diseaseP Lamchiagdhase, P Wilairat, A Bunyaratvej, et al.
Hemoglobin|March 18, 2000
Hb Siam [alpha15(A13)Gly-->Arg] is a GGT-->CGT mutation in the alpha1-globin geneB Yodsowan, J Svast, C Srisomsap, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|December 1, 1982
Heterogeneity of beta thalassaemia in ThailandP Yenchitsomanus, A Baramee, S Fucharoen, et al.
Clinical and Laboratory Haematology|October 16, 2004
Laboratory diagnosis of a compound heterozygosity for Hb Hekinan [alpha27(B8) Glu-Asp] and a deletional alpha-thalassaemia 2 in ThailandS Chunpanich, K Ayukarn, K Sanchaisuriya, et al.
Birth Defects Original Article Series|January 1, 1987
Alpha-mRNA level in the two types of Hb H diseaseP Winichagoon, W Chulalaksananukul, S Panyim, et al.
Acta Endocrinologica|January 1, 1991
Pituitary function in thalassemic patients and the effect of chelation therapyS Vannasaeng, S Fucharoen, P Pootrakul, et al.
Pageof 26