N.B.T. TEST IN OVERWHELMING BACTERIAL INFECTION

بواسطة Warren Lenney, Vinai Suvatte, Soodsakorn Tuchinda
منشور في 2018

Gaucher's disease;thirty-two years experience at Siriraj Hospital

بواسطة Voravarn S. Tanphaichitr, Vinai Suvatte, Chularatana Mahasandana, Prasit Sachapong, Gavivann Veerakul, Suthida Kankirawatana, Pornswan Wasant
منشور في 2018

Successful prophylaxis of intracranial hemorrhage in infants with severe congenital factor VII deficiency

بواسطة Suthida Kankirawatana, Chularatana Mahasandana, Gavivann Veerakul, Julin Seeloem, Lerlugsn Suwantol, Voravan Tanphaichitr, Vinai Suvatte
منشور في 2018

Pyruvate kinase deficiency in an alpha-thalassemia family: First case report in Thailand

بواسطة Voravarn S. Tanphaichitr, Vinai Suvatte, Chularatana Mahasandana, Gavivann Veerakul, Parichat Pung-amritt, Kalya Tachavanich, Hiroshi Ideguchi
منشور في 2018

Dengue hemorrhagic fever in patients with thalassemia

بواسطة Bunchoo Pongtanakul, Nattee Narkbunnam, Gavivann Veerakul, Kleebsabai Sanpakit, Vip Viprakasit, Voravarn Tanphaichitr Tanphaichitr, Vinai Suvatte
منشور في 2018

Malignant lymphoma in Thailand: Changes in the frequency of malignant lymphoma determined from a histopathologic and immunophenotypic analysis of 425 cases at Siriraj Hospital

بواسطة Sanya Sukpanichnant, Dhira Sonakul, Anong Piankijagum, Wanchai Wanachiwanawin, Gavivann Veerakul, Chularatana Mahasandana, Voravarn S. Tanphaichitr, Vinai Suvatte
منشور في 2018

Collection of cord blood stem cells for transplantation in thalassemic patients

بواسطة Surapol Issaragrisil, Sanan Visuthisakchai, Yaowalak Tangnaitrisorana, Anong Piankijagum, Dasnayanee Chandanayingyong, Vinai Suvatte, Voravarn Tanphaichitr, Pornpimol Ruengvuttilert
منشور في 2018

Neonatal purpura fulminans associated with homozygous protein S deficiency

بواسطة Chularatana Mahasandana, Vinai Suvatte, Richard A. Marlar, Marilyn J. Manco-Johnson, Linda J. Jacobson, William E. Hathaway
منشور في 2018

Linear growth in homozygous β-thalassemia and β-thalassemia/hemoglobin E patients under different treatment regimens

بواسطة Vip Viprakasit, Chularatana Mahasandana, Lerlugsn Suwantol, Suthida Kankirawatana, Vinai Suvatte, Voravarn S. Tanphaichitr, Amara Assteerawatt, Gavivann Veerakul, Parichat Pung-Amritt
منشور في 2018

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

بواسطة Supan Fucharoen, Goonnapa Fucharoen, Winionman Sriroongrueng, Vichai Laosombat, Arunee Jetsrisuparb, Sutthipan Prasatkaew, Voravarn S. Tanphaichitr, Vinai Suvatte, Soodsarkorn Tuchinda, Yasuyuki Fukumaki
منشور في 2018

Compound heterozygosity for one novel and one recurrent mutation in a Thai patient with severe protein S deficiency

بواسطة Parichat Pung-Amritt, Swibertus R. Poort, Hans L. Vos, Rogier M. Bertina, Chularatana Mahasandana, Voravarn S. Tanphaichitr, Gavivann Veerakul, Suthida Kankirawatana, Vinai Suvatte
منشور في 2018