Thein SL - Search Results

1

Outcome of children with sickle cell disease admitted to intensive care - a single institution experience.

Bartram JL, Thein SL, Gardner K, Egberongbe Y, D'Silva P, Height SE, Dick MC, O'Driscoll S, Rees DC. Bartram JL, et al. Among authors: thein sl. Br J Haematol. 2010 Sep;150(5):614-7. doi: 10.1111/j.1365-2141.2010.08272.x. Epub 2010 Jun 15. Br J Haematol. 2010. PMID: 20560966 Free article.

2

Hb Sun Prairie: diagnostic pitfalls in thalassemic hemoglobinopathies.

Ho PJ, Rochette J, Rees DC, Fisher CA, Huehns ER, Will AM, Thein SL. Ho PJ, et al. Among authors: thein sl. Hemoglobin. 1996 May;20(2):103-12. doi: 10.3109/03630269609027915. Hemoglobin. 1996. PMID: 8811313

3

Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiency.

Rees DC, Duley J, Simmonds HA, Wonke B, Thein SL, Clegg JB, Weatherall DJ. Rees DC, et al. Among authors: thein sl. Blood. 1996 Oct 1;88(7):2761-7. Blood. 1996. PMID: 8839873 Free article.

4

Erythroblastic inclusions in dominantly inherited beta thalassemias.

Ho PJ, Wickramasinghe SN, Rees DC, Lee MJ, Eden A, Thein SL. Ho PJ, et al. Among authors: thein sl. Blood. 1997 Jan 1;89(1):322-8. Blood. 1997. PMID: 8978308 Free article.

5

Nontransfusional iron overload in thalassemia. Association with hereditary hemochromatosis.

Rees DC, Singh BM, Luo LY, Wickramasinghe S, Thein SL. Rees DC, et al. Among authors: thein sl. Ann N Y Acad Sci. 1998 Jun 30;850:490-4. doi: 10.1111/j.1749-6632.1998.tb10530.x. Ann N Y Acad Sci. 1998. PMID: 9668593 No abstract available.

6

Automated genotyping for accurate assignment of the (AT)xNz(AT)y motif within the beta-globin locus control region-hypersensitive site 2.

Tatu T, Thein S. Tatu T, et al. Br J Haematol. 2001 Feb;112(2):488-92. doi: 10.1046/j.1365-2141.2001.02539.x. Br J Haematol. 2001. PMID: 11167852 Free article.

7

Heterocellular hereditary persistence of fetal haemoglobin affects the haematological parameters of beta-thalassaemia trait.

Garner C, Dew TK, Sherwood R, Rees D, Thein SL. Garner C, et al. Among authors: thein sl. Br J Haematol. 2003 Oct;123(2):353-8. doi: 10.1046/j.1365-2141.2003.04600.x. Br J Haematol. 2003. PMID: 14531920 Free article.

8

Lamin B-receptor mutations in Pelger-Huët anomaly.

Best S, Salvati F, Kallo J, Garner C, Height S, Thein SL, Rees DC. Best S, et al. Among authors: thein sl. Br J Haematol. 2003 Nov;123(3):542-4. doi: 10.1046/j.1365-2141.2003.04621.x. Br J Haematol. 2003. PMID: 14617022 Free article.

9

Pulmonary function abnormalities in children with sickle cell disease.

Sylvester KP, Patey RA, Milligan P, Dick M, Rafferty GF, Rees D, Thein SL, Greenough A. Sylvester KP, et al. Among authors: thein sl. Thorax. 2004 Jan;59(1):67-70. Thorax. 2004. PMID: 14694252 Free PMC article. Clinical Trial.

10

The genetic basis of the interaction between pyrimidine 5' nucleotidase I deficiency and hemoglobin E.

Escuredo E, Marinaki AM, Duley JA, Thein SL, Rees DC. Escuredo E, et al. Among authors: thein sl. Nucleosides Nucleotides Nucleic Acids. 2004 Oct;23(8-9):1261-3. doi: 10.1081/NCN-200027532. Nucleosides Nucleotides Nucleic Acids. 2004. PMID: 15571242

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