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Results: 1-7 |
Results: 7
Mutation causing exon 15 skipping and partial exon 16 deletion in factor VIII transcript, and a method for direct mutation detection
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
Determination of haemophilia A carrier status by mutation analysis
Authors: Oranwiroon, S Akkarapatumwong, V Pung-Amritt, P Treesucon, A Veerakul, G Mahasandana, C Panyim, S Yenchitsomanus, P
Citation: S. Oranwiroon et al., Determination of haemophilia A carrier status by mutation analysis, HAEMOPHILIA, 7(1), 2001, pp. 20-25
Neonatal alloimmune thrombocytopenia due to anti-Nak(a)
Authors: Kankirawatana, S Kupatawintu, P Juji, T Veerakul, G Ngerncham, S Chongkolwatana, V O'Charoen, R
Citation: S. Kankirawatana et al., Neonatal alloimmune thrombocytopenia due to anti-Nak(a), TRANSFUSION, 41(3), 2001, pp. 375-377
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
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
Risultati: 1-7 |