Search Results - "Piankijagum, A"

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  1. 1

    Screening for the carriers of thalassemias and abnormal hemoglobins at the community level by Winichagoon, P, Thitivichianlert, A, Lebnak, T, Piankijagum, A, Fucharoen, S

    “…Thalassemia and abnormal hemoglobins are common genetic disorders in Southeast Asia. Thalassemia is not only an important public health problem but also a…”
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    Relation of haemolytic anaemia and erythrocyte-bound IgG in α- and β-thalassaemic syndromes by Chinprasertsuk, S., Wanachiwanawin, W., Pattanapanyasat, K., Tatsumi, N., Piankijagum, A.

    Published in European journal of haematology (01-02-1997)
    “…: There has been evidence that IgG‐mediated phagocytosis plays some part in destruction of erythroid cells and subsequent anaemia in thalassaemia. In this…”
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  3. 3

    Significance of blood coagulation and platelet profiles in relation to pulmonary thrombosis in beta-thalassemia/Hb E by Visudhiphan, S, Ketsa-Ard, K, Tumliang, S, Piankijagum, A

    “…In beta-Thalassemia hemoglobin E (beta-thal Hb E), hypoxemia with abnormal lung function was described and postmortem examination in these patients showed…”
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    Growth of mixed erythroid-granulocytic colonies in culture derived from bone marrow of patients with paroxysmal nocturnal hemoglobinuria without addition of exogenous stimulator by Issaragrisil, S, Piankijagum, A, Chinprasertsuk, S, Kruatrachue, M

    Published in Experimental hematology (01-10-1986)
    “…Hematopoietic progenitor cell cultures were studied in 16 patients with paroxysmal nocturnal hemoglobinuria (PNH). Both erythroid and granulocyte-macrophage…”
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    Serious complications following treatment of chronic idiopathic thrombocytopenic purpura by Wanachiwanawin, W., Visudhiphan, S., Piankijagum, A., Vatanavicharn, S.

    Published in Postgraduate medical journal (01-06-1988)
    “…Six patients had serious complications as consequences of treatment of idiopathic thrombocytopenic purpura. Five had splenectomy-related complications, one of…”
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    Glomerulonephritis in beta-thalassemia Hb-E disease: clinical manifestations, histopathologic studies and outcome by Ongajyooth, L, Siritanaratkul, N, Pootrakul, P, Parichatikanond, P, Malasit, P, Fucharoen, S, Nimmannit, S, Piankijagum, A, Nilwarangkur, S

    “…We presented 8 patients with beta-thal/Hb E with glomerular diseases. Diverse glomerular lesions were seen, but diffuse endocapillary glomerulonephritis was…”
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  9. 9

    Severe hyperbilirubinemia in glucose-6-phosphate dehydrogenase deficient patients during viral hepatitis by Wanachiwanawin, W, Piankijagum, A

    “…Nine G-6-PD subjects developed acute hemolysis and severe hyperbilirubinemia (up to 61.1 mg/dl) following viral hepatitis. All except one had fever at…”
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    Cytochemical stainings in acute promyelocytic leukemia: chloroacetate esterase reaction as a prognostic index by Chinprasertsuk, S, Piankijagum, A, Issaragrisil, S

    “…Cytochemical studies including peroxidase, sudan black B and esterases were used for staining peripheral blood and bone marrow smears from 42 patients with…”
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    Corticosteroids therapy in paroxysmal nocturnal hemoglobinuria by Issaragrisil, S, Piankijagum, A, Tang-naitrisorana, Y

    Published in American journal of hematology (01-05-1987)
    “…We evaluated the efficacy of alternate day, high dose prednisolone for the treatment of paroxysmal nocturnal hemoglobinuria (PNH). Nineteen patients were…”
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    Dark green pit viper (Trimeresurus popeorum) bite: clinical and serial coagulation profiles in 51 cases by Visudhiphan, S, Tonmukayakul, A, Tumliang, S, Dumavibhat, B, Piankijagum, A

    “…Trimeresurus popeorum, a dark green pit viper, is commonly found in Southeast Asia. This study describes the clinical picture and blood studies of 51 patients…”
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  14. 14

    Outcomes of pregnancy in adult idiopathic thrombocytopenic purpura by Wanachiwanawin, W, Chansung, K, Visudhiphan, S, Piankijagum, A

    “…The outcomes of 39 pregnancies in 36 idiopathic thrombocytopenic purpura (ITP) patients were analysed. Among the 36 pregnant patients, 23 had active ITP…”
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    Methylprednisolone treatment in aplastic anaemia by Issaragrisil, S, Piankijagum, A

    “…Twenty patients with aplastic anaemia were treated with a short term bolus of methylprednisolone. Seven patients were refractory to anabolic steroids and were…”
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    Clinical manifestation of beta-thalassemia/hemoglobin E disease by Fucharoen, S, Ketvichit, P, Pootrakul, P, Siritanaratkul, N, Piankijagum, A, Wasi, P

    Published in Journal of pediatric hematology/oncology (01-11-2000)
    “…To review the clinical manifestation and changes in hematologic parameters of patients with beta-thalassemia/hemoglobin (Hb) E. Retrospective analysis of the…”
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    A syndrome of hypertension, convulsion, and cerebral haemorrhage in thalassaemic patients after multiple blood-transfusions by Wasi, P, Na-Nakorn, S, Pootrakul, P, Sonakul, D, Piankijagum, A, Pacharee, P

    Published in The Lancet (British edition) (16-09-1978)
    “…Various combinations of hypertension, convulsion, severe headache, and cerebral haemorrhage appeared in eight thalassaemic patients after they had received…”
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    Incidence of aplastic anemia in Bangkok. The Aplastic Anemia Study Group by Issaragrisil, S, Sriratanasatavorn, C, Piankijagum, A, Vannasaeng, S, Porapakkham, Y, Leaverton, P E, Kaufman, D W, Anderson, T E, Shapiro, S, Young, N S

    Published in Blood (15-05-1991)
    “…The annual incidence of aplastic anemia in metropolitan Bangkok, Thailand, and its five suburban provinces was prospectively determined. All patients first…”
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    Homozygous haemoglobin Constant Spring: a need for revision of concept by Pootrakul, P, Winichagoon, P, Fucharoen, S, Pravatmuang, P, Piankijagum, A, Wasi, P

    Published in Human genetics (01-01-1981)
    “…Twenty-two patients with mild haemolytic anaemia and haemoglobin (Hb) Constant Spring (CS) of around 6% were studied because they were suspected of having…”
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