Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Napaporn Archararit"'
Autor:
Suporn Chuncharunee, Anusith Tunhasiriwet, Vichai Atichartakarn, Ratchanee Lee, Katcharin Aryurachai, Umaporn Udomsubpayakul, Napaporn Archararit
Publikováno v:
European Journal of Haematology. 92:346-353
To find the prevalence and risk factors of pulmonary hypertension (PHT) in adult patients with hemoglobin E/β-thalassemia disease (E/β-Thal).One hundred and ten clinically stable E/β-Thal outpatients, sixty-one of whom had undergone splenectomy, w
Autor:
Somtawin Sirireung, Arjit Tirakanjana, Nongnuch Sirachainan, Ampaiwan Chuansumrit, Jaruwan Thongsad, Suradej Hongeng, Samart Pakakasama, Praguywan Kadegasem, Napaporn Archararit
Publikováno v:
Thrombosis Research. 129:765-770
The hypercoagulable state is well recognized in patients with severe β-thalassemia disease. One of the mechanisms of chronic hypercoagulable state is the abnormal expression of phosphatidylserine on red blood cells (RBC). This study aimed to determi
Autor:
Buppa Rachakom, Pantep Angchaisuksiri, Arjit Tiraganjana, Vichai Atichartakarn, Katcharin Aryurachai, Kanlayanee Atamasirikul, Napaporn Archararit
Publikováno v:
International Journal of Hematology. 86:397-402
Venous thromboembolism (VTE) has been reported to be less common among Thais than Caucasians. Whether this observation reflects genetic or environmental factors, or both, is uncertain. To identify genetic and acquired risk factors of Thai patients wi
Autor:
Napaporn Archararit, Pantep Angchaisuksiri, Vichai Atichartakarn, Katcharin Aryurachai, Arjit Tiraganjana, Sasivimol Rattanasiri, Suporn Chuncharunee
Publikováno v:
American Journal of Hematology. 82:1001-1004
Increased frequency of thrombosis has been observed in patients with hemoglobin E/beta-thalassemia (Hb E/beta-thal) disease, particularly those who have previously been splenectomized. We compared various hemostatic and thrombotic markers in blood fr
Publikováno v:
Transfusion Medicine. 23:276-278
Autor:
Suporn Chuncharunee, Vichai Atichartakarn, Umaporn Udomsubpayakul, Katcharin Aryurachai, Napaporn Archararit
Publikováno v:
Acta haematologica. 132(1)
The relationship between asplenia and thrombophilia in β-thalassemia disease patients is not yet completely understood. One hundred and ten adult hemoglobin (Hb) E/β-thalassemia (E/β-Thal) disease outpatients, dichotomized according to the presenc
Autor:
Suporn Chuncharunee, Napaporn Archararit, Sutipong Jongjirasiri, Teerapat Yingchoncharoen, Vichai Atichartakarn, Sukit Yamwong, Umaporn Udomsubpayakul
Publikováno v:
Acta haematologica. 130(3)
Autor:
Punnee Butthep, Kovit Pattanapanyasat, Wansa Banyatsuppasin, Vichai Atichartakarn, Suporn Chuncharunee, Napaporn Archararit, Ammarin Thakkinstian
Publikováno v:
American journal of hematology. 86(1)
Aged or abnormal red blood cells with exposed phosphatidylserine (PSRBCs) are cleared from the circulation by splenic macrophages. In asplenic patients, other mononuclear phagocytic cells in tissues and in circulation may function in this capacity. T
Publikováno v:
The Journal of international medical research. 36(6)
The effect of parenteral glutamine dipeptide (Gln) supplementation on neutrophil phagocytosis, superoxide anion generation (SAG), prevention of chemotherapy-induced side-effects and cost-effectiveness was examined in a pilot study of acute myeloid le
Autor:
Pantep Angchaisuksiri, Suchela Janwityanujit, Virunya Parkpian, Oravan Verasertniyom, Kanokrat Nantiruj, Katcharin Ayurachai, Kitti Totemchokchyakarn, Monchand Vanichapuntu, Prapaporn Pisitkul, Napaporn Archararit, Bupha Rachakom
Publikováno v:
Clinical rheumatology. 26(10)
Antibodies to beta(2)-glycoprotein I (anti-beta(2)-GPI) have been reported to have stronger association with clinical antiphospholipid syndrome (APS) than anticardiolipin antibodies (aCL) and lupus anticoagulant (LAC). We investigated the sensitivity