Journal of Inherited Metabolic Disease, 0141-8955

Journal

Publications

  1. 2016
  2. Published
  3. 2012
  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
  6. Published
  7. 2011
  8. Published

    UK experience of liver transplantation for erythropoietic protoporphyria.

    Joanna Dowman & Philip Newsome, 1 Apr 2011, In: Journal of Inherited Metabolic Disease. 34, 2, p. 539-545 7 p.

    Research output: Contribution to journalArticlepeer-review

  9. 2010
  10. Published
  11. 2009
  12. Published
  13. 2008
  14. 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

  15. 2007
  16. 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

  17. 2006
  18. 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

  19. 2004
  20. 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

  21. 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

  22. 2003
  23. Published
  24. 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

  25. 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

  26. 2002
  27. 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

  28. Published

    Mutation screening for tyrosinaemia type 1 - short report

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

    Research output: Contribution to journalArticle

  29. Published
  30. Published
  31. 2001
  32. 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

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