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Malignant lymphoma in Thailand: changes in the frequency of malignant lymphoma determined from a histopathologic and immunophenotypic analysis of 425 cases at Siriraj Hospital
- S. Sukpanichnant, D. Sonakul, A. Piankijagum, W. Wanachiwanawin, G. Veerakul, C. Mahasandana
- 15 November 1998
BACKGROUND Analysis of malignant lymphoma in a single institution at different periods of time can determine the changing status of the disease in the region. METHODS To compare with the large… Expand
Clinical Manifestation of &bgr;-Thalassemia/Hemoglobin E Disease
- S. Fucharoen, P. Ketvichit, P. Pootrakul, N. Siritanaratkul, A. Piankijagum, P. Wasi
- Journal of pediatric hematology/oncology
- 1 November 2000
Purpose To review the clinical manifestation and changes in hematologic parameters of patients with &bgr;-thalassemia/hemoglobin (Hb) E. Materials and Methods Retrospective analysis of the clinical… Expand
Screening for the carriers of thalassemias and abnormal hemoglobins at the community level.
- P. Winichagoon, A. Thitivichianlert, T. Lebnak, A. Piankijagum, S. Fucharoen
- The Southeast Asian journal of tropical medicine…
Thalassemia and abnormal hemoglobins are common genetic disorders in Southeast Asia. Thalassemia is not only an important public health problem but also a socio-economic problem of many countries in… Expand
Incidence of aplastic anemia in Bangkok. The Aplastic Anemia Study Group.
The annual incidence of aplastic anemia in metropolitan Bangkok, Thailand, and its five suburban provinces was prospectively determined. All patients first diagnosed during the period from January… Expand
Agranulocytosis in Bangkok, Thailand: a predominantly drug-induced disease with an unusually low incidence. Aplastic Anemia Study Group.
- S. Shapiro, S. Issaragrisil, +9 authors N. Young
- The American journal of tropical medicine and…
- 1 April 1999
Agranulocytosis, a syndrome characterized by a marked reduction in circulating granulocytes, is strongly associated with medical drug use in Europe and the United States. Unregulated use of common… Expand
Brief report: transplantation of cord-blood stem cells into a patient with severe thalassemia.
- S. Issaragrisil, S. Visuthisakchai, +6 authors A. Piankijagum
- The New England journal of medicine
- 9 February 1995
Several different kinds of thalassemia and hemoglobinopathy are prevalent in Southeast Asia.1,2 The frequency of the α-thalassemias reaches 30 to 40 percent in northern Thailand, whereas the… Expand
Prenatal and postnatal diagnoses of thalassemias and hemoglobinopathies by HPLC.
The conventional approach to qualitative and quantitative analyses of hemoglobin (Hb) molecules for the diagnoses of hemoglobinopathies requires a combination of tests. We used an automated HPLC… Expand
Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in beta-thalassemia/hemoglobin E disease.
Hydroxyurea (HU) is one of several agents that have been shown to enhance hemoglobin (Hb) F levels in patients with sickle cell disease and may be useful as a therapy for beta-globinopathies.… Expand
Infection in thalassemia: a retrospective study of 1,018 patients with beta-thalassemia/Hb E disease.
Fatal arteritis due to Pythium insidiosum infection in patients with thalassaemia.
- W. Wanachiwanawin, M. Thianprasit, +5 authors A. Piankijagum
- Transactions of the Royal Society of Tropical…
- 1 May 1993
Six thalassaemic patients had a distinct clinical syndrome characterized by progressive ischemia of the lower extremities, with ascending arteritis and thrombosis of the main arteries of the lower… Expand