Homozygous protein S deficiency: 7-year follow-up [3]

بواسطة C. Mahasandana, G. Veerakul, V. S. Tanphaichitr, V. Suvatte, N. Opartkiattikul, W. E. Hathaway
منشور في 2018

Mutation causing exon 15 skipping and partial exon 16 deletion in factor VIII transcript, and a method for direct mutation detection

بواسطة P. Yenchitsomanus, P. Thanootarakul, V. Akkarapatumwong, S. Oranwiroon, P. Pung-Amritt, G. Veerakul, C. Mahasandana
منشور في 2018

Successful bone marrow transplantation in a child with red blood cell pyruvate kinase deficiency

بواسطة V. S. Tanphaichitr, V. Suvatte, S. Issaragrisil, C. Mahasandana, G. Veerakul, V. Chongkolwatana, W. Waiyawuth, H. Ideguchi
منشور في 2018

Determination of haemophilia A carrier status by mutation analysis

بواسطة S. Oranwiroon, V. Akkarapatumwong, P. Pung-Amritt, A. Treesucon, G. Veerakul, C. Mahasandana, S. Panyim, P. Yenchitsomanus
منشور في 2018

Mutations of the factor VIII gene in thai hemophilia A patients

بواسطة V. Akkarapatumwong, S. Oranwiroon, P. Pung-amritt, A. Treesucon, P. Thanootarakul, G. Veerakul, C. Mahasandana, S. Panyim, P. Yenchitsomanus
منشور في 2018