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1
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Determination for different severity of anemia in thalassemia: Concordance and discordance among sib pairs
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2
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2 Wasi P, Pootrakul P, Fucharoen S, Winichagoon P, Wilairat P, Promboon A: Thalassemia in Southeast Asia: determination of different degrees of severity of anemia in thalassemia. Ann N Y Acad Sci 1985, 445:119-126.
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5 Fucharoen S, Ketvichit P, Pootrakul P, Siritanaratkul N, Piankijagum A, Wasi P: The clinical manifestation of β-thalassemia/Hb E disease. J Pediatr Hematol Oncol 1999, in press.
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Quantitative assessment of erythropoiesis and functional classification of anemia based on measurements of serum transferrin receptor and erythropoietin
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Spinal cord compression in thalassemia: Report of 12 cases and recommendation for treatment
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7 Issaragrisil S, Piankijagum A, Wasi P: Spinal cord compression in thalassemia: report of 12 cases and recommendation for treatment. Arch Intern Med 1981, 141:1033-1036.
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Intracranial extramedullary hematopoiesis inducing epilepsy in a patient with β-thalassemia-hemoglobin E
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8 Fucharoen S, Suthipongchai S, Poungvarin N, Ladpli S, Sonakul D, Wasi P: Intracranial extramedullary hematopoiesis inducing epilepsy in a patient with β-thalassemia-hemoglobin E. Arch Intern Med 1985, 145:739-742.
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9 Pootrakul P, Hungsprenges S, Fucharoen S, Baylink D, Thompson E, English E, et al.: Relation between erythropoiesis and bone metabolism in thalassemia. N Engl J Med 1981, 304:1470-1473.
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0023480699
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Patients with thalassemia develop osteoporosis, osteomalacia, and hypoparathyroidism, all of which are corrected by transfusion
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10 Christensen RA, Pootrakul P, Burrnell JM, Teuner EJ, Finch CA, Baylink DJ: Patients with thalassemia develop osteoporosis, osteomalacia, and hypoparathyroidism, all of which are corrected by transfusion. Birth Defects 1988, 23:409-416.
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11
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4243212873
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Iron overload in Hb E- β-thalassemia: Magnetic measurement of hepatic iron stores
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11 Brittenham G, Pootrakul P, Finch CA, Yansukon P, Kitcharoen K, Fucharoen S, et al.: Iron overload in Hb E-β-thalassemia: magnetic measurement of hepatic iron stores [abstract]. Blood 1986, 68:72.
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12 Pootrakul P, Huebers HA, Finch CA, Pippard MJ, Cazzola M: Iron metabolism in thalassemia. Birth Defects 1988, 23:3-8.
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13 Pootrakul P, Kitcharoen K, Yansukon P, Wasi P, Fucharoen S, Charoenlarp P, et al.: The effect of erythroid hyperplasia on iron balance. Blood 1988, 71:1124-1129.
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14
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Histochemical study of liver tissue from thalassemic patients
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14 Thakerngpol K, Sonakul D, Fucharoen S, Vathanopas V, Stinimankarn T: Histochemical study of liver tissue from thalassemic patients. Birth Defects 1988, 23:193-198.
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15
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0023763811
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Electron microscopic study of liver tissue from 30 thalassemic patients
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15 Thakerngpol K, Sonakul D, Fucharoen S, Boonyaphiphat P, Vathanopas V, Sahaphong S, Stitnimankarn T: Electron microscopic study of liver tissue from 30 thalassemic patients. Birth Defects 1988, 23:199-206.
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16
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0023613682
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Impaired glucose counter regulation after insulin induced hypoglycemia in thalassemia patients
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16 Vannasaeng S, Fucharoen S, Nitiyanant W, Vichayanrat A, Pootrakul P, Piraphatdist T: Impaired glucose counter regulation after insulin induced hypoglycemia in thalassemia patients. J Med Assoc Thailand 1987, 70:631-637.
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17
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0023476073
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Oxidative stress and antioxidants in β-thalassemia/hemoglobin E
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17 Suthipark K, Ong-ajyooth S, Shumnumsirivath D, Likidlilid A, Fucharoen S, Siddhikol C, et al.: Oxidative stress and antioxidants in β-thalassemia/hemoglobin E. Birth Defects 1988, 23:199-205.
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18
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0032533264
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Oxidative modification of low-density lipoprotein and atherogenetic risk in β-thalassemia
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18 Livrea MA, Tesoriere L, Maggio A, D'Arpa D, Pintaudi AM, Pedone E: Oxidative modification of low-density lipoprotein and atherogenetic risk in β-thalassemia. Blood 1998, 92:3936-3942.
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19
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0021605407
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Cardiac pathology in 47 patients with beta thalassemia/hemoglobin E
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19 Sonakul D, Pacharee P, Wasi P, Fucharoen S: Cardiac pathology in 47 patients with beta thalassemia/hemoglobin E. Southeast Asian J Trop Med Public Health 1984, 15:554-563.
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20
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Apolipoprotein E ε4 allele as a genetic risk factor for left ventricular failure in homozygous β-thalassemia
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20 Economou-Petersen E, Aessopos A, Kladi A, Flevari P, Karabatsos F, Fragodimitri C, et al.: Apolipoprotein E ε4 allele as a genetic risk factor for left ventricular failure in homozygous β-thalassemia. Blood 1998, 92:3455-3459.
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21
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0025441923
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Cardiac involvement in beta-thalassemia/hemoglobin E disease: Clinical and hemodynamic findings
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21 Jootar P, Fucharoen S: Cardiac involvement in beta-thalassemia/hemoglobin E disease: clinical and hemodynamic findings. Southeast Asian J Trop Med Public Health 1990, 21:269-273.
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Deaths in β-thalassemia/Hb E patients secondary to infections
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22 Fucharoen S, Piankijagum A, Wasi P: Deaths in β-thalassemia/Hb E patients secondary to infections. Birth Defects 1988, 23:495-500.
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Infection in thalassemia: A retrospective study of 1,018 patients with β-thalassemia/Hb E disease
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23 Issaragrisil S, Wanachiwanawin W, Bhuripanyo K, Benjasuratwong Y, Piankijagum A, Wasi P: Infection in thalassemia: a retrospective study of 1,018 patients with β-thalassemia/Hb E disease. Birth Defects 1988, 23:505-511.
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24
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0023513146
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A study of infective episodes in patients with β-thalassemia/Hb E disease in Thailand
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24 Aswapokee N, Aswapokee P, Fucharoen S, Wasi P: A study of infective episodes in patients with β-thalassemia/Hb E disease in Thailand. Birth Defects 1988, 23:513-520.
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25
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0023465522
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Severe infection in thalassemia: A prospective study
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25 Aswapokee P, Aswapokee N, Fucharoen S, Sukroongreung S, Wasi P: Severe infection in thalassemia: a prospective study. Birth Defects 1988, 23:521-526.
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26
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0023465224
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Viral infections in β-thalassemia/hemoglobin E patients
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26 Wasi C, Kuntang R, Louisirirotchanakul S, Siritantikorn S, Fucharoen S, Aswapokee P: Viral infections in β-thalassemia/hemoglobin E patients. Birth Defects 1988, 23:547-555.
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27
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0027257923
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Fatal arteritis due to pythium insidiosum infection in patients with thalassemia
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27 Wanachiwanawin W, Thianprasit M, Fucharoen S, Chaiprasert A, Sudasna N, Ayuthaya N, et al.: Fatal arteritis due to pythium insidiosum infection in patients with thalassemia. Trans R Soc Trop Med Hyg 1993, 87:296-298.
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28
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0027137877
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Activation of monocytes for the immune clearance of red cells in β̊-thalassemia/HbE
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28 Wanachiwanawin W, Siripanyaphinyo U, Fucharoen S, Wasi P, Mawas F, Wiener E, Wickramasinghe SN: Activation of monocytes for the immune clearance of red cells in β̊-thalassemia/HbE. Br J Haematol 1993, 85:773-777.
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29
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Lymphocytes in β-thalassemia/Hb E: Subpopulations and mitogen responses
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29 Wanachiwanawin W, Chucharoen J, Pattanapanyasat K, Fucharoen S, Webster HK: Lymphocytes in β-thalassemia/Hb E: subpopulations and mitogen responses. Eur J Haematol 1996, 55:153-157.
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30
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0032979966
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Serum levels of tumor necrosis factor- α, interleukin-1, and interferon- in β̊-thalassemia/Hb E and their clinical significance
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30 Wanachiwanawin W, Wiener E, Siripanyaphinyo U, Chinprasertsuk S, Mawas F, Fucharoen S, et al.: Serum levels of tumor necrosis factor-α, interleukin-1, and interferon-in β̊-thalassemia/Hb E and their clinical significance. J Interferon Cytokine Res 1999, 19:1050-1011.
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31
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Presence of immunoglobulins, C3 and cytolytic C5b-9 complement components on the surface of erythrocytes from patients with β-thalassaemia/Hb E disease
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31 Malasit P, Mahasorn W, Mongkolsapaya J, Singhathong B, Fucharoen S, Wasi P, Bhakdi S: Presence of immunoglobulins, C3 and cytolytic C5b-9 complement components on the surface of erythrocytes from patients with β-thalassaemia/Hb E disease. Br J Haematol 1997, 96:507-513.
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A syndrome of hypertension, convulsion and cerebral haemorrhage in thalassaemic patients after multiple blood-transfusions
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33
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Study of mechanisms of post-transfusion hypertension in thalassaemic patients
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33 Thirawarapan S, Snongchart N, Fucharoen S, Tanphaichitr VS, Dhorranintra B: Study of mechanisms of post-transfusion hypertension in thalassaemic patients. Southeast Asian J Trop Med Public Health 1989, 20:471-478.
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Brain pathology in 6 fatal cases of post-transfusion hypertension, convulsion and cerebral hemorrhage syndrome
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34 Sonakul D, Fucharoen S: Brain pathology in 6 fatal cases of post-transfusion hypertension, convulsion and cerebral hemorrhage syndrome. Southeast Asian J Trop Med Public Health 1992, 23(Suppl 2):116-119.
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37 Sonakul D, Pacharee P, Laohapand T, Fucharoen S, Wasi P: Pulmonary artery obstruction in thalassaemia. Southeast Asian J Trop Med Public Health 1980, 11:516-523.
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39
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0023475845
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Distribution of pulmonary thromboembolic lesions in thalassemic patients
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39 Sonakul D, Suwanagool P, Sirivaidyapong P, Fucharoen S: Distribution of pulmonary thromboembolic lesions in thalassemic patients. Birth Defects 1988, 23:375-384.
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0027024167
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Increase in spontaneous platelet aggregation in β-thalassemia/hemoglobin E disease: A consequence of splenectomy
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40 Opartkiattikul N, Funahara Y, Fucharoen S, Thalalak P: Increase in spontaneous platelet aggregation in β-thalassemia/hemoglobin E disease: a consequence of splenectomy. Southeast Asian J Trop Med Public Health 1992, 23(Suppl 2):36-41.
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0027024753
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Detection of PF3 availability in whole blood from volunteers and β-thalassemia/HbE patients: A promising method for prediction of thrombolytic tendency
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41 Opartkiattikul N, Funahara Y, Hijikata-Okunomiya A, Yamaguchi A, Fucharoen S, Talalak P: Detection of PF3 availability in whole blood from volunteers and β-thalassemia/HbE patients: a promising method for prediction of thrombolytic tendency. Southeast Asian J Trop Med Public Health 1992, 23(Suppl 2):52-59.
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42
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0027023687
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Protein C and protein S deficiency in thalassemic patients
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42 Shirahata A, Funahara Y, Opartkiattikul N, Fucharoen S, Laosombat V, Yamada K: Protein C and protein S deficiency in thalassemic patients. Southeast Asian J Trop Med Public Health 1992, 23(Suppl 2):65-73.
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18744422490
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Interaction between endothelial cells and thalassemic red cells in vitro
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43 Butthep P, Bunyaratvej A, Kitaguchi H, Funahara Y, Fucharoen S: Interaction between endothelial cells and thalassemic red cells in vitro. Southeast Asian J Trop Med Public Health 1992, 23(Suppl 2):101-104.
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Alterations in vascular endothelial cell-related plasma proteins in thalassaemic patients and their correlation with clinical symptoms
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44 Butthep P, Bunyaratvej A, Funahara Y, Kitaguchi H, Fucharoen S, Sato S, Bhamarapravati N: Alterations in vascular endothelial cell-related plasma proteins in thalassaemic patients and their correlation with clinical symptoms. Thromb Haemost 1995, 74:1045-1049.
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55 Fucharoen S, Siritanaratkul N, Winichagoon P, Chowthaworn J, Siriboon W, Muangsup W, et al.: Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in β-thalassemia/hemoglobin E disease. Blood 1996, 87:887-892.
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