Simmonds HA - Search Results

1

Usefulness of intact erythrocyte studies in the diagnosis of inherited purine and pyrimidine defects.

Fairbanks LD, Simmonds HA, Webster DR. Fairbanks LD, et al. Among authors: simmonds ha. Adv Exp Med Biol. 1986;195 Pt A:101-7. doi: 10.1007/978-1-4684-5104-7_16. Adv Exp Med Biol. 1986. PMID: 2425562 No abstract available.

2

Inosine formation from hypoxanthine by intact erythrocytes and fibroblasts of an immunodeficient child with purine nucleoside phosphorylase deficiency.

Fairbanks LD, Webster DR, Simmonds HA, Potter CF, Watson AR. Fairbanks LD, et al. Among authors: simmonds ha. Adv Exp Med Biol. 1984;165 Pt B:167-70. doi: 10.1007/978-1-4757-0390-0_33. Adv Exp Med Biol. 1984. PMID: 6426263 No abstract available.

3

Screening for purine and pyrimidine disorders using dried urine spots.

Fairbanks LD, Escuredo E, Duley JA, Simmonds HA. Fairbanks LD, et al. Among authors: simmonds ha. Adv Exp Med Biol. 2000;486:383-8. doi: 10.1007/0-306-46843-3_73. Adv Exp Med Biol. 2000. PMID: 11783520 No abstract available.

4

Correlations between purine levels, clinical and immunological status in ADA deficiency.

Simmonds HA, Fairbanks LD, Morris GS, Hugh-Jones K, Morgan G, Levinsky RJ. Simmonds HA, et al. Adv Exp Med Biol. 1986;195 Pt A:93-9. doi: 10.1007/978-1-4684-5104-7_15. Adv Exp Med Biol. 1986. PMID: 3728190 No abstract available.

5

Purine and pyrimidine metabolism in hereditary oroticaciduria during a 15 year follow-up study.

Webster DR, Simmonds HA, Potter CF, Becroft DM. Webster DR, et al. Among authors: simmonds ha. Adv Exp Med Biol. 1979;122B:203-8. doi: 10.1007/978-1-4684-8559-2_34. Adv Exp Med Biol. 1979. PMID: 546145 No abstract available.

6

HPLC assay of uridine monophosphate synthase (UMPS) in chorionic villus samples (CVS) and erythrocytes (RBC).

Fairbanks LD, Duley JA, Shores AJ, Simmonds HA. Fairbanks LD, et al. Among authors: simmonds ha. Adv Exp Med Biol. 1991;309B:35-8. doi: 10.1007/978-1-4615-7703-4_8. Adv Exp Med Biol. 1991. PMID: 1781395 No abstract available.

7

Importance of the human erythrocyte in the diagnosis of inherited purine and pyrimidine disorders.

Simmonds HA, Fairbanks LD, Duley JA, Micheli V. Simmonds HA, et al. Biomed Biochim Acta. 1990;49(2-3):S259-64. Biomed Biochim Acta. 1990. PMID: 2386515

8

Use of intact erythrocytes in the diagnosis of inherited purine and pyrimidine disorders.

Fairbanks LD, Simmonds HA, Webster DR. Fairbanks LD, et al. Among authors: simmonds ha. J Inherit Metab Dis. 1987;10(2):174-86. doi: 10.1007/BF01800045. J Inherit Metab Dis. 1987. PMID: 2443757

9

Further evidence for a 'new' purine defect, inosine triphosphate (ITP) pyrophosphohydrolase deficiency.

Simmonds HA, Micheli V, Duley JA, Fairbanks LD, Hopkinson DA, Levinsky RJ. Simmonds HA, et al. Adv Exp Med Biol. 1989;253A:97-102. doi: 10.1007/978-1-4684-5673-8_15. Adv Exp Med Biol. 1989. PMID: 2560342 No abstract available.

10

Source and fate of circulating pyrimidines.

Harley EH, Sacks S, Berman P, Cohen L, Simmonds HA, Fairbanks LD, Black D. Harley EH, et al. Among authors: simmonds ha. Adv Exp Med Biol. 1986;195 Pt A:109-13. doi: 10.1007/978-1-4684-5104-7_17. Adv Exp Med Biol. 1986. PMID: 3014828 No abstract available.

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