Thein SL - Search Results

1

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

2

Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency.

Sumi S, Marinaki AM, Arenas M, Fairbanks L, Shobowale-Bakre M, Rees DC, Thein SL, Ansari A, Sanderson J, De Abreu RA, Simmonds HA, Duley JA. Sumi S, et al. Among authors: thein sl. Hum Genet. 2002 Oct;111(4-5):360-7. doi: 10.1007/s00439-002-0798-z. Epub 2002 Aug 15. Hum Genet. 2002. PMID: 12384777

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

Genetic basis of hemolytic anemia caused by pyrimidine 5' nucleotidase deficiency.

Marinaki AM, Escuredo E, Duley JA, Simmonds HA, Amici A, Naponelli V, Magni G, Seip M, Ben-Bassat I, Harley EH, Thein SL, Rees DC. Marinaki AM, et al. Among authors: thein sl. Blood. 2001 Jun 1;97(11):3327-32. doi: 10.1182/blood.v97.11.3327. Blood. 2001. PMID: 11369620 Free article.

5

The effects of air quality on haematological and clinical parameters in children with sickle cell anaemia.

Mittal H, Roberts L, Fuller GW, O'Driscoll S, Dick MC, Height SE, Thein SL, Rees DC. Mittal H, et al. Among authors: thein sl. Ann Hematol. 2009 Jun;88(6):529-33. doi: 10.1007/s00277-008-0598-1. Epub 2008 Sep 4. Ann Hematol. 2009. PMID: 18769920

6

g(HbF): a genetic model of fetal hemoglobin in sickle cell disease.

Gardner K, Fulford T, Silver N, Rooks H, Angelis N, Allman M, Nkya S, Makani J, Howard J, Kesse-Adu R, Rees DC, Stuart-Smith S, Yeghen T, Awogbade M, Sangeda RZ, Mgaya J, Patel H, Newhouse S, Menzel S, Thein SL. Gardner K, et al. Among authors: thein sl. Blood Adv. 2018 Feb 13;2(3):235-239. doi: 10.1182/bloodadvances.2017009811. Blood Adv. 2018. PMID: 29437638 Free PMC article.

7

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.

8

Nontransfusional iron overload in thalassemia: association with hereditary hemochromatosis.

Rees DC, Luo LY, Thein SL, Singh BM, Wickramasinghe S. Rees DC, et al. Among authors: thein sl. Blood. 1997 Oct 15;90(8):3234-6. Blood. 1997. PMID: 9376610 Free article. No abstract available.

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

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.

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