Wraith JE - Search Results

1

No sensory neuropathy during pyridoxine treatment in homocystinuria.

Mpofu C, Alani SM, Whitehouse C, Fowler B, Wraith JE. Mpofu C, et al. Among authors: wraith je. Arch Dis Child. 1991 Sep;66(9):1081-2. doi: 10.1136/adc.66.9.1081. Arch Dis Child. 1991. PMID: 1929522 Free PMC article.

2

Carpal tunnel syndrome in the mucopolysaccharidoses and related disorders.

Wraith JE, Alani SM. Wraith JE, et al. Arch Dis Child. 1990 Sep;65(9):962-3. doi: 10.1136/adc.65.9.962. Arch Dis Child. 1990. PMID: 2121106 Free PMC article.

3

Mutation analysis in 46 British and Irish patients with Gaucher's disease.

Hatton CE, Cooper A, Whitehouse C, Wraith JE. Hatton CE, et al. Among authors: wraith je. Arch Dis Child. 1997 Jul;77(1):17-22. doi: 10.1136/adc.77.1.17. Arch Dis Child. 1997. PMID: 9279145 Free PMC article.

4

Magnetic resonance imaging of the brain in phenylketonuria.

Cleary MA, Walter JH, Wraith JE, Jenkins JP, Alani SM, Tyler K, Whittle D. Cleary MA, et al. Among authors: wraith je. Lancet. 1994 Jul 9;344(8915):87-90. doi: 10.1016/s0140-6736(94)91281-5. Lancet. 1994. PMID: 7912392

5

Methionine and serine formation in control and mutant human cultured fibroblasts: evidence for methyl trapping and characterization of remethylation defects.

Fowler B, Whitehouse C, Wenzel F, Wraith JE. Fowler B, et al. Among authors: wraith je. Pediatr Res. 1997 Jan;41(1):145-51. doi: 10.1203/00006450-199701000-00023. Pediatr Res. 1997. PMID: 8979304

6

A terminal deletion of 11q.

Schwarz C, Mpofu C, Wraith JE. Schwarz C, et al. Among authors: wraith je. J Med Genet. 1992 Jul;29(7):511-2. J Med Genet. 1992. PMID: 1640436 Free PMC article. No abstract available.

7

A patient with severe type of epimerase deficiency galactosaemia.

Sardharwalla IB, Wraith JE, Bridge C, Fowler B, Roberts SA. Sardharwalla IB, et al. Among authors: wraith je. J Inherit Metab Dis. 1988;11 Suppl 2:249-51. doi: 10.1007/BF01804249. J Inherit Metab Dis. 1988. PMID: 3141714 No abstract available.

8

Niemann-Pick disease type C in adults.

Imrie J, Vijayaraghaven S, Whitehouse C, Harris S, Heptinstall L, Church H, Cooper A, Besley GT, Wraith JE. Imrie J, et al. Among authors: wraith je. J Inherit Metab Dis. 2002 Oct;25(6):491-500. doi: 10.1023/a:1021259403196. J Inherit Metab Dis. 2002. PMID: 12555942

9

The natural history of Niemann-Pick disease type C in the UK.

Imrie J, Dasgupta S, Besley GT, Harris C, Heptinstall L, Knight S, Vanier MT, Fensom AH, Ward C, Jacklin E, Whitehouse C, Wraith JE. Imrie J, et al. Among authors: wraith je. J Inherit Metab Dis. 2007 Feb;30(1):51-9. doi: 10.1007/s10545-006-0384-7. Epub 2006 Dec 11. J Inherit Metab Dis. 2007. PMID: 17160617

10

Absence of acidosis in the initial presentation of propionic acidaemia.

Walter JH, Wraith JE, Cleary MA. Walter JH, et al. Among authors: wraith je. Arch Dis Child Fetal Neonatal Ed. 1995 May;72(3):F197-9. doi: 10.1136/fn.72.3.f197. Arch Dis Child Fetal Neonatal Ed. 1995. PMID: 7796239 Free PMC article.

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