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

由 C. Mahasandana, G. Veerakul, V. S. Tanphaichitr, V. Suvatte, N. Opartkiattikul, W. E. Hathaway
出版 2018

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

由 P. Yenchitsomanus, P. Thanootarakul, V. Akkarapatumwong, S. Oranwiroon, P. Pung-Amritt, G. Veerakul, C. Mahasandana
出版 2018

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

由 V. S. Tanphaichitr, V. Suvatte, S. Issaragrisil, C. Mahasandana, G. Veerakul, V. Chongkolwatana, W. Waiyawuth, H. Ideguchi
出版 2018

Determination of haemophilia A carrier status by mutation analysis

由 S. Oranwiroon, V. Akkarapatumwong, P. Pung-Amritt, A. Treesucon, G. Veerakul, C. Mahasandana, S. Panyim, P. Yenchitsomanus
出版 2018

Mutations of the factor VIII gene in thai hemophilia A patients

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