J. Wildgoose

P2i (United Kingdom) — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index320citations18works1.02yr avg
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Research Topics

Metabolism and Genetic Disorders(13), Diet and metabolism studies(10), Amino Acid Enzymes and Metabolism(4), Muscle metabolism and nutrition(3), Mitochondrial Function and Pathology(2)

Publications16 total

S2 What is the clinical effectiveness and cost-effectiveness of nebulised 7% saline in patients with chronic obstructive pulmonary disease (COPD)- (MucAct COPD Trial)
2025· 1 cited
Phenylalanine free infant formula in the dietary management of phenylketonuria
Orphanet Journal of Rare Diseases·2023· 9 citedOpen Access
P31 Minor reformulations of infant food for special medical purposes due to EU regulations 2016/127 & 2016/128 are well tolerated, accepted, complied with and continue to support growth in infants & children requiring nutrition support
Poster presentations·2021Open Access
Uniformity of Food Protein Interpretation Amongst Dietitians for Patients with Phenylketonuria (PKU): 2020 UK National Consensus Statements
Nutrients·2020· 16 citedOpen Access
Mealtime Anxiety and Coping Behaviour in Parents and Children during Weaning in PKU: A Case-Control Study
Nutrients·2019· 13 citedOpen Access
Growth, Protein and Energy Intake in Children with PKU Taking a Weaning Protein Substitute in the First Two Years of Life: A Case-Control Study
Nutrients·2019· 27 citedOpen Access
How Does Feeding Development and Progression onto Solid Foods in PKU Compare with Non-PKU Children During Weaning?
Nutrients·2019· 17 citedOpen Access
Practices in prescribing protein substitutes for PKU in Europe: No uniformity of approach
Molecular Genetics and Metabolism·2015· 35 cited
How strict is galactose restriction in adults with galactosaemia? International practice
Molecular Genetics and Metabolism·2015· 16 cited
Dietary practices in pyridoxine non-responsive homocystinuria: A European survey
Molecular Genetics and Metabolism·2013· 25 cited
Dietary management of urea cycle disorders: European practice
Molecular Genetics and Metabolism·2013· 52 cited
Dietary management of urea cycle disorders: UK practice
Journal of Human Nutrition and Dietetics·2012· 27 cited
Weaning infants with phenylketonuria: a review
Journal of Human Nutrition and Dietetics·2011· 31 cited
DIETARY MANAGEMENT OF NON-PYRIDOXINE RESPONSIVE HOMOCYSTINURIA
Data Archiving and Networked Services (DANS)·2011
The Exeter half-day release psychotherapy training scheme – a model for others?
Psychiatric Bulletin·2002· 11 citedOpen Access
Eccentric exercise and neuroleptic malignant syndrome
The Lancet·1998· 1 cited

Frequent Co-authors

Sharon Evans(11), Anita MacDonald(11), Anne Daly(8), Barbara Cochrane(8), Louise Robertson(7), Allyson Terry(7), Sarah Adam(5), Marjorie Dixon(5), Diana Webster(5), F. White(5), H. Zweers(5), Catherine Ashmore(5), Manuela Almeida(4), Helena Champion(4), Katharina Dokoupil(4), Ana Faria(4), Christine S. Ferguson(4), M. Heddrich‐Ellerbrok(4), C.M. Jankowski(4), S F Lowry(4)