V. Tanphaichitr

发表

Rapid flow cytometric test using eosin-5-maleimide for diagnosis of red blood cell membrane disorders.

V. Viprakasit, K. Tachavanich, V. Tanphaichitr, 2009, The Southeast Asian journal of tropical medicine and public health.

Hemodynamic responses to captopril during splenectomy in thalassemic children.

S. Pirayavaraporn, V. Tanphaichitr, V. Suwanchinda, 1999, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Molecular basis of β-thalassemia in Thailand: analysis of β-thalassemia mutations using the polymerase chain reaction

Y. Fukumaki, V. Suvatte, V. Tanphaichitr, 1989, Human Genetics.

Recurrent A353V mutation in a Thai family with X-linked dyskeratosis congenita.

V. Viprakasit, V. Tanphaichitr, 2001, Haematologica.

Deferiprone (GPO‐L‐ONE®) monotherapy reduces iron overload in transfusion‐dependent thalassemias: 1‐year results from a multicenter prospective, single arm, open label, dose escalating phase III pediatric study (GPO‐L‐ONE; A001) from Thailand

Prapat Suriyaphol, A. Chuansumrit, J. Pooliam, 2013, American journal of hematology.

Malignancies in HIV-infected children at Siriraj Hospital.

K. Sanpakit, C. Mahasandana, G. Veerakul, 2002, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Malignant lymphoma in Thailand

C. Mahasandana, V. Suvatte, G. Veerakul, 1998 .

Baseline levels of plasma endothelin‐1 (ET‐1) and changes during transfusion in thalassemic patients

V. Viprakasit, P. Akarasereenont, K. Durongpisitkul, 2002, American journal of hematology.

Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemia.

M. Weiss, D. Higgs, V. Viprakasit, 2004, Blood.

Early detection of cardiac involvement in beta-thalassemia children.

K. Durongpisitkul, V. Tanphaichitr, C. Kangkagate, 2002, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Brief report: transplantation of cord-blood stem cells into a patient with severe thalassemia.

V. Suvatte, D. Chandanayingyong, S. Kanokpongsakdi, 1995, The New England journal of medicine.

Renal tubular function in beta-thalassemia.

P. Malasit, S. Pattanakitsakul, V. Tanphaichitr, 1998, Pediatric nephrology.

Direct detection for G6PD Bangkok and G6PD Bangkok Noi mutations in the families with chronic nonspherocytic hemolytic anemia (CNSHA)

V. Tanphaichitr, W. Thongnoppakhun, A. Treesucon, 2015, International journal of laboratory hematology.

Novel AE1 mutations in recessive distal renal tubular acidosis. Loss-of-function is rescued by glycophorin A.

S. Alper, C. Brugnara, G. Veerakul, 1998, The Journal of clinical investigation.

Acquired platelet dysfunction with eosinophilia: study of platelet function in 62 cases.

C. Mahasandana, V. Suvatte, V. Tanphaichitr, 1979, The Southeast Asian journal of tropical medicine and public health.

Penicilliosis-associated hemophagocytic syndrome in a human immunodeficiency virus-infected child: the first case report in children.

A. Chaiprasert, G. Veerakul, K. Chokephaibulkit, 2001, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Bone marrow transplantation for thalassemia in Thailand.

C. Mahasandana, V. Suvatte, D. Chandanayingyong, 1993, Bone marrow transplantation.

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

V. Tanphaichitr, W. Wanachiwanawin, A. Treesucon, 2011, Annals of Hematology.

Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression.

S. Philipsen, D. Higgs, V. Viprakasit, 2014, Blood.

Incidence of Ototoxicity in Pediatric Patients with Transfusion-Dependent Thalassemia Who Are Less Well-Chelated by Mono- and Combined Therapy of Iron Chelating Agents

J. Pooliam, V. Viprakasit, V. Tanphaichitr, 2014, Hemoglobin.

Renal tubular dysfunction in α-thalassemia

P. Malasit, V. Tanphaichitr, S. Ong-ajyooth, 2003, Pediatric Nephrology.

Renal tubular function in β-thalassemia

P. Malasit, S. Pattanakitsakul, V. Tanphaichitr, 1998, Pediatric nephrology (Berlin, West).

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

V. Viprakasit, V. Tanphaichitr, Kevin D. Clark, 2002, European journal of haematology.

Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from Thailand

V. Viprakasit, M. Sirikong, P. Ruangvutilert, 2013, Clinical chemistry and laboratory medicine.

Clinical and hematological phenotype of homozygous hemoglobin E: revisit of a benign condition with hidden reproductive risk.

V. Viprakasit, K. Tachavanich, V. Tanphaichitr, 2009, The Southeast Asian journal of tropical medicine and public health.

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

V. Viprakasit, P. Yenchitsomanus, V. Tanphaichitr, 2005 .

Validation of osmotic fragility test and dichlorophenol indophenol precipitation test for screening of thalassemia and Hb E.

S. Sangkitporn, V. Tanphaichitr, S. Sangkitporn, 2005, The Southeast Asian journal of tropical medicine and public health.

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

V. Viprakasit, V. Tanphaichitr, W. Chinchang, 2004 .

V. Viprakasit, K. Tachavanich, V. Tanphaichitr, 2002, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Clinical phenotypes and molecular characterization of Hb H-Paksé disease.

D. Higgs, V. Viprakasit, C. Fisher, 2002, Haematologica.

Homozygous Hemoglobin Tak Causes Symptomatic Secondary Polycythemia in a Thai Boy

V. Viprakasit, K. Sanpakit, G. Veerakul, 2003, Journal of pediatric hematology/oncology.

Common origin of a rare β‐globin initiation codon mutation (ATG→AGG) in Asians

V. Viprakasit, V. Tanphaichitr, W. Chinchang, 2005 .

Combination of chemotherapy, radiotherapy and immunotherapy for acute lymphoblastic leukemia in children.

C. Mahasandana, V. Suvatte, V. Tanphaichitr, 1981, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Recent advances in diagnosis of paragonimiasis.

N. Tatsumi, S. Sukpanichnant, V. Tanphaichitr, 1997 .

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

V. Viprakasit, K. Tachavanich, V. Tanphaichitr, 2002, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Transient, acquired glucose-6-phosphate dehydrogenase deficiency in Thai children with typhoid fever.

C. Mahasandana, V. Suvatte, V. Tanphaichitr, 1982, The Southeast Asian journal of tropical medicine and public health.

Compound Heterozygosity for One Novel and One Recurrent Mutation in a Thai Patient with Severe Protein S Deficiency

R. Bertina, C. Mahasandana, V. Suvatte, 1999, Thrombosis and Haemostasis.

Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.

R. Chapman, Jennifer J. Pointon, V. Viprakasit, 2003, Human molecular genetics.

Secondary hemophagocytic lymphohistiocytosis in children: an analysis of etiology and outcome.

K. Sanpakit, C. Mahasandana, G. Veerakul, 2002, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

Successful treatment of cytophagic histiocytic panniculitis by cyclosporin A: a case report.

V. Tanphaichitr, W. Wisuthsarewong, J. Manonukul, 1997, Asian Pacific journal of allergy and immunology.

Identification of mutations in the uroporphyrinogen III synthase gene in a Thai girl patient with congenital erythropoietic porphyria

V. Tanphaichitr, W. Thongnoppakhun, A. Treesucon, 2015, International journal of laboratory hematology.

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

V. Viprakasit, P. Yenchitsomanus, K. Tachavanich, 2004, European journal of haematology.

Clinical Phenotypes and Molecular Diagnosis in a Hitherto Interaction of Hb E / β Thalassemia Syndrome ( β E / β-31 , A → G )

V. Viprakasit, G. Veerakul, V. Tanphaichitr, 2005 .

COMPOUND HETEROZYGOSITY FOR α0-THALASSEMIA (−−THAI) AND Hb CONSTANT SPRING CAUSES SEVERE Hb H DISEASE

V. Viprakasit, V. Tanphaichitr, 2002, Hemoglobin.

Vitamin B12 deficiency: report of a childhood case.

V. Tanphaichitr, S. Areekul, S. Sirimachan, 1991, Journal of the Medical Association of Thailand = Chotmaihet thangphaet.

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

V. Viprakasit, P. Yenchitsomanus, V. Tanphaichitr, 2005, Clinical biochemistry.

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

D. Higgs, V. Viprakasit, G. Veerakul, 2004, American journal of hematology.

Renal tubular dysfunction in alpha-thalassemia.

P. Malasit, V. Tanphaichitr, S. Ong-ajyooth, 2003, Pediatric nephrology (Berlin, West).

Acute haemolytic crisis in a Thai patient with homozygous haemoglobin Constant Spring (Hb CS/CS): a case report

V. Viprakasit, K. Sanpakit, G. Veerakul, 2004, Annals of tropical paediatrics.

INITIATION CODON MUTATION (ATG!A-G) OF THE a2 GENE CAUSES Hb H DISEASE IN THAILAND

V. Viprakasit, V. Tanphaichitr, W. Chinchang, 2005 .

Collection of cord blood stem cells for transplantation in thalassemic patients

V. Suvatte, D. Chandanayingyong, V. Tanphaichitr, 1995, Stem cells.

Common origin of a rare beta-globin initiation codon mutation (ATG-->AGG) in Asians.

V. Viprakasit, V. Tanphaichitr, W. Chinchang, 2005, Clinical and laboratory haematology.

Successful bone marrow transplantation in a child with red blood cell pyruvate kinase deficiency

C. Mahasandana, V. Suvatte, G. Veerakul, 2000, Bone Marrow Transplantation.

Hemoglobin constant spring in bangkok: Molecular screening by selective enzymatic amplification of the α2‐globin gene

S. Fucharoen, P. Winichagoon, S. Embury, 1991, American journal of hematology.

Immunogenicity and protective efficacy of low dose recombinant DNA hepatitis B vaccine in normal and high-risk neonates.

V. Suvatte, V. Tanphaichitr, V. Tanphaichitr, 1991, Asian Pacific journal of allergy and immunology.

A Rare Association of α0-Thalassemia (– –SEA) and an Initiation Codon Mutation (ATG→A-G) of the α2 Gene Causes Hb H Disease in Thailand

V. Viprakasit, V. Tanphaichitr, W. Glomglao, 2005 .

Bone marrow, peripheral blood and cord blood stem cell transplantation in children: ten years' experience at Siriraj Hospital.

C. Mahasandana, V. Suvatte, D. Chandanayingyong, 1998, International journal of hematology.

Purification of human hemopoietic stem cells for transplantation in Thailand.

K. Pattanapanyasat, V. Tanphaichitr, S. Issaragrisil, 2000, Asian Pacific Journal of Allergy and Immunology.

Immunogenicity and efficacy of a recombinant DNA hepatitis B vaccine, GenHevac B Pasteur in high risk neonates, school children and healthy adults.

V. Suvatte, V. Tanphaichitr, V. Tanphaichitr, 1993, Asian Pacific journal of allergy and immunology.

A. Chuansumrit, J. Pooliam, S. Srichairatanakool, 2013, American journal of hematology.

Hypertension posttransfusion in Thai thalassemic children: early detection and management.

C. Mahasandana, V. Suvatte, V. Tanphaichitr, 1988, Birth defects original article series.

Prevalence of hemoglobin E, alpha-thalassemia and glucose-6-phosphate dehydrogenase deficiency in 1,000 cord bloods studied in Bangkok.

C. Mahasandana, V. Suvatte, V. Tanphaichitr, 1995, The Southeast Asian journal of tropical medicine and public health.

Hereditary Methemoglobinemia Due to Cytochrome b5 Reductase Deficiency

G. Veerakul, V. Tanphaichitr, Kleebsabai Sanpakit, 2004 .

Incidence of Ototoxicity in Pediatric Patients with Transfusion-Dependent Thalassemia Who Are Less Well-Chelated by Mono- and Combined Therapy of Iron Chelating Agents

J. Pooliam, V. Viprakasit, V. Tanphaichitr, 2014, Hemoglobin.

Sinus histiocytosis with massive lymphadenopathy: the first three cases reported in Thailand.

C. Mahasandana, V. Suvatte, S. Sukpanichnant, 1990, Asian Pacific journal of allergy and immunology.