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Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH‐cytochrome b5 reductase gene

British journal of haematology, 1998-12, Vol.103 (4), p.922-930

1998

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Complex interactions of δβ hybrid haemoglobin (Hb Lepore‐Hollandia) Hb E (β26 G→A) and α+ thalassaemia in a Thai family

European journal of haematology, 2002-02, Vol.68 (2), p.107-111

2002

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Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder

European journal of haematology, 2004-07, Vol.73 (1), p.43-49

2004

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Co‐inheritance of Hb Pak Num Po, a novel α1 gene mutation, and α0 thalassemia associated with transfusion‐dependent Hb H disease

American journal of hematology, 2004-03, Vol.75 (3), p.157-163

2004

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Frameshift mutations with severe and moderate clinical phenotypes in Thai hemophilia A patients

Human mutation, 2000-12, Vol.16 (6), p.530-531

2000

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A Novel Asn344 Deletion in the Core Domain of Coagulation Factor XIII A Subunit: Its Effects on Protein Structure and Function

Blood, 1998-07, Vol.92 (2), p.481-487

1998

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Compound heterozygosity for one novel and one recurrent mutation in a Thai patient with severe protein S deficiency

Thrombosis and haemostasis, 1999-02, Vol.81 (2), p.189

1999

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Clinical phenotypes and molecular characterization of Hb H-Paksé disease

Haematologica (Roma), 2002-02, Vol.87 (2), p.117

2002

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Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok Noi

Annals of hematology, 2011-07, Vol.90 (7), p.769-775

2011

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Molecular analysis of unknown β-globin gene mutations using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique and its application in Thai families with β-thalassemias and β-globin variants

Clinical biochemistry, 2005-11, Vol.38 (11), p.987-996

2005

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DEVELOPMENT OF A COMPREHENSIVE RED BLOOD CELL ENZYMOPATHY LABORATORY IN THAILAND : THE STUDY OF NORMAL ACTIVITY IN EIGHT ERYTHROENZYMES IN THAIS

Southeast Asian journal of tropical medicine and public health, 2009-03, Vol.40 (2), p.317-326

2009

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A Novel Asn344 Deletion in the Core Domain of Coagulation Factor XIII A Subunit: Its Effects on Protein Structure and Function

Blood, 1998-07, Vol.92 (2), p.481-487

1998

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Linear growth in homozygous beta-thalassemia and beta-thalassemia/hemoglobin E patients under different treatment regimens

Journal of the Medical Association of Thailand, 2001-07, Vol.84 (7), p.929-941

2001

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Identification of Hb Q-India (64 Asp→His) in Thailand

Hematology (Luxembourg), 2004-04, Vol.9 (2), p.151-155

2004

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Co‐inheritance of Hb Pak Num Po, a novel α1 gene mutation, and α 0 thalassemia associated with transfusion‐dependent Hb H disease

American journal of hematology, 2004-03, Vol.75 (3), p.157-163

2004

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Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease

American journal of hematology, 2004-03, Vol.75 (3), p.157-163

2004

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Effect of red blood cell glucose-6-phosphate dehydrogenase deficiency on patients with dengue hemorrhagic fever

Journal of the Medical Association of Thailand, 2002-08, Vol.85 Suppl 2, p.S522-S529

2002

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Co-inheritance of Hb Pak Num Po, a novel alpha 1 gene mutation, and alpha super(0) thalassemia associated with transfusion-dependent Hb H disease

American journal of hematology, 2004-01, Vol.75 (3), p.157-163

2004

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Prevalence of HB E from cord blood samples and after one year follow-up

Southeast Asian journal of tropical medicine and public health, 1999, Vol.30 Suppl 2, p.97-99

1999

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Complex interactions of deltabeta hybrid haemoglobin (Hb Lepore-Hollandia) Hb E (beta(26G-->A)) and alpha+ thalassaemia in a Thai family

European journal of haematology, 2002-02, Vol.68 (2), p.107-111

2002

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The validation of an automated liquid chromatography system for the diagnosis of thalassemias and hemoglobinopathies

Southeast Asian journal of tropical medicine and public health, 2002-12, Vol.33 (4), p.862-868

2002

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Carrier detection by DNA linkage analysis in eighty Thai hemophilia A families

Journal of the Medical Association of Thailand, 2002-08, Vol.85 Suppl 2, p.S513-S521

2002

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Allele related mutation specific-polymerase chain reaction for rapid diagnosis of Hb New York (beta 113 (G15) Val-->Glu, beta(CD113 GTG-->GAG))

Journal of the Medical Association of Thailand, 2002-08, Vol.85 Suppl 2, p.S558-S563

2002

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Pyruvate kinase deficiency in an alpha-thalassemia family : First case report in Thailand

Southeast Asian journal of tropical medicine and public health, 1997, Vol.28, p.64-68

1997

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Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH‐cytochrome b 5 reductase gene

British journal of haematology, 1998-12, Vol.103 (4), p.922-930

1998

Link zum Volltext

Verfügbarkeit prüfen

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Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH‐cytochrome b5 reductase gene

Complex interactions of δβ hybrid haemoglobin (Hb Lepore‐Hollandia) Hb E (β26 G→A) and α+ thalassaemia in a Thai family

Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder

Co‐inheritance of Hb Pak Num Po, a novel α1 gene mutation, and α0 thalassemia associated with transfusion‐dependent Hb H disease

Frameshift mutations with severe and moderate clinical phenotypes in Thai hemophilia A patients

A Novel Asn344 Deletion in the Core Domain of Coagulation Factor XIII A Subunit: Its Effects on Protein Structure and Function

Compound heterozygosity for one novel and one recurrent mutation in a Thai patient with severe protein S deficiency

Clinical phenotypes and molecular characterization of Hb H-Paksé disease

Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok Noi

Molecular analysis of unknown β-globin gene mutations using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique and its application in Thai families with β-thalassemias and β-globin variants

DEVELOPMENT OF A COMPREHENSIVE RED BLOOD CELL ENZYMOPATHY LABORATORY IN THAILAND : THE STUDY OF NORMAL ACTIVITY IN EIGHT ERYTHROENZYMES IN THAIS

A Novel Asn344 Deletion in the Core Domain of Coagulation Factor XIII A Subunit: Its Effects on Protein Structure and Function

Linear growth in homozygous beta-thalassemia and beta-thalassemia/hemoglobin E patients under different treatment regimens

Identification of Hb Q-India (64 Asp→His) in Thailand

Co‐inheritance of Hb Pak Num Po, a novel α1 gene mutation, and α 0 thalassemia associated with transfusion‐dependent Hb H disease

Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease

Effect of red blood cell glucose-6-phosphate dehydrogenase deficiency on patients with dengue hemorrhagic fever

Co-inheritance of Hb Pak Num Po, a novel alpha 1 gene mutation, and alpha super(0) thalassemia associated with transfusion-dependent Hb H disease

Prevalence of HB E from cord blood samples and after one year follow-up

Complex interactions of deltabeta hybrid haemoglobin (Hb Lepore-Hollandia) Hb E (beta(26G-->A)) and alpha+ thalassaemia in a Thai family

The validation of an automated liquid chromatography system for the diagnosis of thalassemias and hemoglobinopathies

Carrier detection by DNA linkage analysis in eighty Thai hemophilia A families

Allele related mutation specific-polymerase chain reaction for rapid diagnosis of Hb New York (beta 113 (G15) Val-->Glu, beta(CD113 GTG-->GAG))

Pyruvate kinase deficiency in an alpha-thalassemia family : First case report in Thailand

Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH‐cytochrome b 5 reductase gene

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