Authors:
Yenchitsomanus, P
Thanootarakul, P
Akkarapatumwong, V
Oranwiroon, S
Pung-Amritt, P
Veerakul, G
Mahasandana, C
Citation: P. Yenchitsomanus et al., Mutation causing exon 15 skipping and partial exon 16 deletion in factor VIII transcript, and a method for direct mutation detection, HAEMOPHILIA, 7(3), 2001, pp. 335-338
Authors:
Tanphaichitr, VS
Suvatte, V
Issaragrisil, S
Mahasandana, C
Veerakul, G
Chongkolwatana, V
Waiyawuth, W
Ideguchi, H
Citation: Vs. Tanphaichitr et al., Successful bone marrow transplantation in a child with red blood cell pyruvate kinase deficiency, BONE MAR TR, 26(6), 2000, pp. 689-690
Authors:
Pung-amritt, P
Poor, SR
Vos, HL
Bertina, RM
Mahasandana, C
Tanphaichitr, VS
Veerakul, G
Kankirawatana, S
Suvatte, V
Citation: P. Pung-amritt et al., Compound heterozygosity for one novel and one recurrent mutation in a Thaipatient with severe protein S deficiency, THROMB HAEM, 81(2), 1999, pp. 189-192
Authors:
Suvatte, V
Tanphaichitr, VS
Visuthisakchai, S
Mahasandana, C
Veerakul, G
Chongkolwatana, V
Chandanayingyong, D
Issaragrisil, S
Citation: V. Suvatte et al., Bone marrow, peripheral blood and cord blood stem cell transplantation in children: Ten years' experience at Siriraj Hospital, INT J HEMAT, 68(4), 1998, pp. 411-419
Authors:
Tanphaichitr, VS
Sumboonnanonda, A
Ideguchi, H
Shayakul, C
Brugnara, C
Takao, M
Veerakul, G
Alper, SL
Citation: Vs. Tanphaichitr et al., Novel AE1 mutations in recessive distal renal tubular acidosis - Loss-of-function is rescued by glycophorin A, J CLIN INV, 102(12), 1998, pp. 2173-2179