Journal of Inherited Metabolic Disease, ‎0141-8955

Journal

Publications

  1. Published

    'Ready to drink' protein substitute is easier is for people with phenylketonuria

    Pete Davies, , , , , & , 1 Aug 2006, In: Journal of Inherited Metabolic Disease. 29, 4, p. 526-531 6 p.

    Research output: Contribution to journalArticle

  2. Published

    A new, low-volume protein substitute for teenagers and adults with phenylketonuria

    1 Jan 2004, In: Journal of Inherited Metabolic Disease. 27, p. 127-135 9 p.

    Research output: Contribution to journalArticle

  3. Published
  4. Published

    Bile acid-CoA ligase deficiency-a new inborn error of bile acid metabolism

    Paul Gissen, , , & , 1 May 2012, In: Journal of Inherited Metabolic Disease. 35, 3, p. 521-530 10 p.

    Research output: Contribution to journalArticle

  5. Published

    Free use of fruits and vegetables in phenylketonuria

    Ian Booth, 1 Jan 2003, In: Journal of Inherited Metabolic Disease. 26, p. 327-338 12 p.

    Research output: Contribution to journalArticle

  6. Published
  7. Published
  8. Published

    Late presentation of medium-chain acyl-CoA dehydrogenase deficiency.

    Louisa Edwards, & , 1 Feb 2007, In: Journal of Inherited Metabolic Disease. 30, 1, p. 104 1 p.

    Research output: Contribution to journalArticle

  9. Published

    Long-term compliance with a novel vitamin and mineral supplement in older people with PKU

    1 Dec 2008, In: Journal of Inherited Metabolic Disease. 31, 6, p. 718-723 6 p.

    Research output: Contribution to journalArticle

  10. Published

    Mutation screening for tyrosinaemia type 1 - short report

    1 Jan 2002, In: Journal of Inherited Metabolic Disease. 24

    Research output: Contribution to journalArticle

  11. Published

    Mutation screening for tyrosinaemia type I.

    Richard Gray, , , Elizabeth Walker & , 1 Oct 2002, In: Journal of Inherited Metabolic Disease. 25, 6, p. 523-4 2 p.

    Research output: Contribution to journalArticle

  12. Published
  13. Published

    Ophthalmic follow-up in patients with tyrosinaemia type 1on NTBC

    Paul Gissen, , & , 1 Jan 2001, In: Journal of Inherited Metabolic Disease. 24, p. 32 1 p.

    Research output: Contribution to journalAbstract

  14. Published

    Ophthalmic follow-up of patients with tyrosinaemia type I on NTBC.

    Paul Gissen, , & , 1 Jan 2003, In: Journal of Inherited Metabolic Disease. 26, 1, p. 13-6 4 p.

    Research output: Contribution to journalArticle

  15. Published

    Outcome of Tyrosinaemia type III

    1 Jan 2001, In: Journal of Inherited Metabolic Disease. 24, p. 824-832 9 p.

    Research output: Contribution to journalArticle

  16. Published
  17. Published

    Prenatal diagnosis of succinate semialdehyde dehydrogenase deficiency in non-identical twins

    Irene Aligianis, , , , Mark Kilby, & , 1 Jan 2002, In: Journal of Inherited Metabolic Disease. 25(6), p. 517-518 2 p.

    Research output: Contribution to journalArticle

  18. Published

    Protein substitutes for PKU: what's new?

    Ian Booth, 1 Jan 2004, In: Journal of Inherited Metabolic Disease. 27, p. 363-361

    Research output: Contribution to journalArticle

  19. Published
  20. Published

    Treatment of complicated hyperlipidaemia in patients with glycogen storage disease Type 1A

    Paul Gissen, , , & , 1 Jan 2002, In: Journal of Inherited Metabolic Disease. 25, p. 126 1 p.

    Research output: Contribution to journalArticle

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