Simmonds HA - Search Results

1

Adenosine deaminase (ADA) deficiency as the unexpected cause of CD4+ T-lymphocytopenia in two HIV-negative adult female siblings.

Fairbanks LD, Simmonds HA, Webster AD, Shovlin CL, Hughes JM. Fairbanks LD, et al. Among authors: simmonds ha. Adv Exp Med Biol. 1994;370:471-4. doi: 10.1007/978-1-4615-2584-4_100. Adv Exp Med Biol. 1994. PMID: 7660952 No abstract available.

2

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.

3

Biochemical and immunological status following gene therapy and PEG-ADA therapy for adenosine deaminase (ADA) deficiency.

Fairbanks LD, Simmonds HA, Hoogerbrugge PM, van Beusechem VW, Valerio D, Moseley A, Levinsky RJ, Gaspar HB, Morgan G. Fairbanks LD, et al. Among authors: simmonds ha. Adv Exp Med Biol. 1994;370:391-4. doi: 10.1007/978-1-4615-2584-4_85. Adv Exp Med Biol. 1994. PMID: 7660936 No abstract available.

4

Adenosine deaminase deficiency with altered biochemical parameters in two sisters with late-onset immunodeficiency.

Fairbanks LD, Shovlin CL, Webster AD, Hughes JM, Simmonds HA. Fairbanks LD, et al. Among authors: simmonds ha. J Inherit Metab Dis. 1994;17(1):135-7. doi: 10.1007/BF00735418. J Inherit Metab Dis. 1994. PMID: 7914248 No abstract available.

5

Carrier erythrocyte entrapped adenosine deaminase therapy in adenosine deaminase deficiency.

Bax BE, Bain MD, Fairbanks LD, Simmonds HA, Webster AD, Chalmers RA. Bax BE, et al. Among authors: simmonds ha. Adv Exp Med Biol. 2000;486:47-50. doi: 10.1007/0-306-46843-3_9. Adv Exp Med Biol. 2000. PMID: 11783525 No abstract available.

6

ADA activity and DATP levels in erythrocytes after bone marrow transplantation.

Fairbanks LD, Simmonds HA, Duley JA, Gaspar HB, Flood T, Steward CA. Fairbanks LD, et al. Among authors: simmonds ha. Adv Exp Med Biol. 2000;486:51-5. doi: 10.1007/0-306-46843-3_10. Adv Exp Med Biol. 2000. PMID: 11783527 No abstract available.

7

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.

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

ATP formation from deoxyadenosine in human erythrocytes: evidence for a hitherto unidentified route involving adenine and S-adenosylhomocysteine hydrolase.

Simmonds HA, Fairbanks LD, Duley JA, Morris GS. Simmonds HA, et al. Biosci Rep. 1989 Feb;9(1):75-85. doi: 10.1007/BF01117513. Biosci Rep. 1989. PMID: 2785825

10

First trimester diagnosis of adenosine deaminase deficiency.

Dooley T, Fairbanks LD, Simmonds HA, Rodeck CH, Nicolaides KH, Soothill PW, Stewart P, Morgan G, Levinsky RJ. Dooley T, et al. Among authors: simmonds ha. Prenat Diagn. 1987 Oct;7(8):561-5. doi: 10.1002/pd.1970070806. Prenat Diagn. 1987. PMID: 3120171

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