AAAAAA

   
Results: 1-7 |
Results: 7
Recurrent A353V mutation in a Thai family with X-linked dyskeratosis congenita
Authors: Viprakasit, V Tanphaichitr, VS
Citation: V. Viprakasit et Vs. Tanphaichitr, Recurrent A353V mutation in a Thai family with X-linked dyskeratosis congenita, HAEMATOLOG, 86(8), 2001, pp. 871-872
Successful bone marrow transplantation in a child with red blood cell pyruvate kinase deficiency
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
Purification of human hemopoietic stem cells for transplantation in Thailand
Authors: Udomsakdi-Auewarakul, C U-pratya, Y Chongkolwatana, V Tanphaichitr, VS Pattanapanyasat, K Issaragrisil, S
Citation: C. Udomsakdi-auewarakul et al., Purification of human hemopoietic stem cells for transplantation in Thailand, A P J ALLER, 18(2), 2000, pp. 85-92
Compound heterozygosity for one novel and one recurrent mutation in a Thaipatient with severe protein S deficiency
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
Bone marrow, peripheral blood and cord blood stem cell transplantation in children: Ten years' experience at Siriraj Hospital
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
Novel AE1 mutations in recessive distal renal tubular acidosis - Loss-of-function is rescued by glycophorin A
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
Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH-cytochrome b(5) reductase gene
Authors: Higasa, K Manabe, J Yubisui, T Sumimoto, H Pung-amritt, P Tanphaichitr, VS Fukumaki, Y
Citation: K. Higasa et al., Molecular basis of hereditary methaemoglobinaemia, types I and II: two novel mutations in the NADH-cytochrome b(5) reductase gene, BR J HAEM, 103(4), 1998, pp. 922-930
Risultati: 1-7 |