Acquired von Willebrand disease in Wilms' tumor patients von COPPES, M. J, ZANDVOORT, S. W. H, SPARLING, C. R, POON, A. O, WEITZMAN, S, BLANCHETTE, V. S

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Reticulated platelet counts in the diagnosis of acute immune thrombocytopenic purpura von SAXON, B. R, BLANCHETTE, V. S, BUTCHART, S, LIM-YIN, J, POON, A. O

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Reduction of plasma volume after storage of platelets in CP2D von Rock, G., Haddad, S.A., Poon, A.O., Romans, R.A., Sparling, C.R., Louis, P., Berger, R.

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Acute tumour lysis syndrome with no evidence of tumour load von HAIN, R. D. W, HARVEY, E, POON, A. O, WEITZMAN, S

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Coagulation plasma factor levels are early indicators of graft nonfunction following liver transplantation in children von Bilik, Ron, Superina, Riccardo A., Poon, A.O.

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An α-Globin Gene Initiation Codon Mutation in a Black Family With HbH Disease von Olivieri, Nancy F., Chang, Lebe S., Poon, AnnetteO, Michelson, Alan M., Orkin, Stuart H.

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Hyperkalaemia during massive blood transfusion in paediatric craniofacial surgery von BROWN, K. A, BISSONNETTE, B, MACDONALD, M, POON, A. O

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Diagnosis of small bowel radiation enteritis by capsule endoscopy von Lee, D W H, Poon, A O S, Chan, A C W

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An alpha-globin gene initiation codon mutation in a black family with HbH disease von Olivieri, NF, Chang, LS, Poon, AO, Michelson, AM, Orkin, SH

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Compound Heterozygosity for two Genotypes of α-Thalassemia-2 : Hematological, Biosynthetic and DNA Studies von Wong, S. C., Chang, L. S., Olivieri, N. F., Poon, A. O., Ali, M. A. M., Groves, D. J.

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666 Two previously uncharacterized double heterozygous states for hemoglobin E von Carcao, M. D., Al-Hashmi, I. M., Waye, J. S., Muraca, M. F., Poon, A. O., Olivieri, N. F.

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Hb E/Hb LeporeHollandia in a family from Bangladesh von Waye, John S., Eng, Barry, Patterson, Margaret, Chui, David H. K., Chang, Lebe S., Cogionis, Bessie, Poon, Annette O., Olivieri, Nancy F.

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Hb E/Hb lepore Hollandia in a family from Bangladesh von WAYE, J. S, ENG, B, PATTERSON, M, CHUI, D. H. K, CHANG, L. S, COGIONIS, B, POON, A. O, OLIVIERI, N. F

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Coagulation plasma factor levels are early indicators of graft nonfunction following liver transplantation in children. Discussion von BILIK, R, SUPERINA, R. A, POON, A. O, DUNN, S, BILIK, R

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A new frameshift beta zero-thalassemia mutation (codons 27-28 +C) found in a Chinese family von Cai, S P, Chui, D H, Ng, J, Poon, A O, Freedman, M H, Olivieri, N F

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A new frameshift β°‐thalassemia mutation (codons 27–28 +C) found in a Chinese family von Cai, Shiping, Chui, David H. K., Ng, Judy, Poon, Annette O., Freedman, Melvin H., Olivieri, Nancy F.

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A Second Observation of the Fetal Methehoglobin Variant HB F-M-Fort Ripley or α2Gγ292(F8)HIS→TYR von Molchanova, T. P., Wilson, J. B., Gu, L-H., Hain, R. D. W., Chang, L. S., Poon, A. O., Huisman, T. H. J.

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A second observation of the fetal methemoglobin variant Hb F-M-Fort Ripley or α2Gγ292(F8)His→Tyr von MOLCHANOVA, T. P, WILSON, J. B, GU, L.-H, HAIN, R. D. W, CHANG, L. S, POON, A. O, HUISMAN, T. H. J

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A second observation of the fetal methemoglobin variant Hb F-M-Fort Ripley or alpha 2G gamma 2(92)(F8)His----Tyr von Molchanova, T P, Wilson, J B, Gu, L H, Hain, R D, Chang, L S, Poon, A O, Huisman, T H

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A Second Observation of the Fetal Methehoglobin Variant HB F-M-Fort Ripley or α 2 G γ 2 92 (F8)HIS→TYR von Molchanova, T. P., Wilson, J. B., Gu, L-H., Hain, R. D. W., Chang, L. S., Poon, A. O., Huisman, T. H. J.

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