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Antenatal diagnosis of inborn errors of metabolism.
Cleary MA, Wraith JE. Cleary MA, et al. Arch Dis Child. 1991 Jul;66(7 Spec No):816-22. doi: 10.1136/adc.66.7_spec_no.816. Arch Dis Child. 1991. PMID: 1863132 Free PMC article. No abstract available.
Immune function in prolidase deficiency.
Cleary MA, Heaney M, Couriel JM, Walter JH. Cleary MA, et al. J Inherit Metab Dis. 1994;17(3):345-8. doi: 10.1007/BF00711826. J Inherit Metab Dis. 1994. PMID: 7807949 No abstract available.
Management of mucopolysaccharidosis type III.
Cleary MA, Wraith JE. Cleary MA, et al. Arch Dis Child. 1993 Sep;69(3):403-6. doi: 10.1136/adc.69.3.403. Arch Dis Child. 1993. PMID: 8215557 Free PMC article. Review. No abstract available.
Histidinaemia: a benign metabolic disorder.
Lam WK, Cleary MA, Wraith JE, Walter JH. Lam WK, et al. Among authors: cleary ma. Arch Dis Child. 1996 Apr;74(4):343-6. doi: 10.1136/adc.74.4.343. Arch Dis Child. 1996. PMID: 8669938 Free PMC article.
Generalised uridine diphosphate galactose-4-epimerase deficiency.
Walter JH, Roberts RE, Besley GT, Wraith JE, Cleary MA, Holton JB, MacFaul R. Walter JH, et al. Among authors: cleary ma. Arch Dis Child. 1999 Apr;80(4):374-6. doi: 10.1136/adc.80.4.374. Arch Dis Child. 1999. PMID: 10086948 Free PMC article.
153 results