List of works - Fiona White

Blood phenylalanine control in adolescents with phenylketonuria.

scientific article

Complete reversal of moderate/severe brain MRI abnormalities in a patient with classical phenylketonuria.

scientific article published in July 1997

Daily variation in food intake of infants from 2 to 18 months

scientific article published on 01 December 1983

Dietary management of urea cycle disorders: European practice.

scientific article published on 12 September 2013

Dietary practices in isovaleric acidemia: A European survey

scientific article published on 27 February 2017

Dietary practices in propionic acidemia: A European survey

scientific article published on 3 October 2017

Dietary practices in pyridoxine non-responsive homocystinuria: a European survey.

scientific article published on 10 October 2013

How practical are recommendations for dietary control in phenylketonuria?

scientific article

Increased risk of vitamin B12 deficiency in patients with phenylketonuria on an unrestricted or relaxed diet

scientific article published on 01 April 2000

Magnetic resonance imaging in phenylketonuria: reversal of cerebral white matter change

scientific article published on 01 August 1995

Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approach.

scientific article published on 26 March 2015

Randomised controlled trial of essential fatty acid supplementation in phenylketonuria.

scientific article published on 8 March 2006

Review of specialist dietitian services in patients with inherited metabolic disease in the United Kingdom.

scientific article published on April 2007

Strategies for the treatment of cystathionine beta-synthase deficiency: the experience of the Willink Biochemical Genetics Unit over the past 30 years

scientific article published on 01 April 1998

The use of continuous glucose monitoring in the practical management of glycogen storage disorders

scientific article published on 10 May 2011

Unsuccessful treatment of severe pyruvate carboxylase deficiency with triheptanoin.