Camille Newby

Bristol Royal Hospital for Children — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

7h-index177citations16works1.62yr avg
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Research Topics

Metabolism and Genetic Disorders(14), Diet and metabolism studies(10), Folate and B Vitamins Research(6), Mitochondrial Function and Pathology(3), Infant Nutrition and Health(3)

Publications16 total

OC42 Classical homocystinuria (HCU) presenting with complications of chronic pancreatitis
2025
Corrigendum to “The effects of casein glycomacropeptide on general health status in children with PKU: A randomized crossover trial” [Molecular Genetics and Metabolism Volume 143, Issue 4, December 2024, 108607]
Molecular Genetics and Metabolism·2025Open Access
Human Milk Feeding in Inherited Metabolic Disorders: A Systematic Review of Growth, Metabolic Control, and Neurodevelopment Outcomes
Journal of Inherited Metabolic Disease·2025· 4 citedOpen Access
UK Patient Access to Low-Protein Prescription Foods in Phenylketonuria (PKU): An Uneasy Path
Nutrients·2025· 1 citedOpen Access
The effects of casein glycomacropeptide on general health status in children with PKU: A randomized crossover trial
Molecular Genetics and Metabolism·2024· 3 citedOpen Access
Evaluation of a New ‘Mix-In’ Style Glycomacropeptide-Based Protein Substitute for Food and Drinks in Patients with Phenylketonuria and Tyrosinemia
Nutrients·2023· 4 citedOpen Access
Evaluation of a New Glycomacropeptide-Based Protein Substitute in Powdered and Liquid Format in Patients with PKU
Nutrients·2023· 4 citedOpen Access
Introducing a granule based protein substitute to the diet of a child with phenylketonuria to address reluctance to ingest phenylalanine-free protein substitute: A case report
Nutrition and Health·2023· 5 citedOpen Access
Suitability and Allocation of Protein-Containing Foods According to Protein Tolerance in PKU: A 2022 UK National Consensus
Nutrients·2022· 7 citedOpen Access
Special Low Protein Foods Prescribed in England for PKU Patients: An Analysis of Prescribing Patterns and Cost
Nutrients·2021· 21 citedOpen Access
Dietary Management, Clinical Status and Outcome of Patients with Citrin Deficiency in the UK
Nutrients·2020· 23 citedOpen Access
Uniformity of Food Protein Interpretation Amongst Dietitians for Patients with Phenylketonuria (PKU): 2020 UK National Consensus Statements
Nutrients·2020· 16 citedOpen Access
Nutritional and Metabolic Characteristics of UK Adult Phenylketonuria Patients with Varying Dietary Adherence
Nutrients·2019· 37 citedOpen Access
Development of national consensus statements on food labelling interpretation and protein allocation in a low phenylalanine diet for PKU
Orphanet Journal of Rare Diseases·2019· 13 citedOpen Access
Weaning practices in phenylketonuria vary between health professionals in Europe
Molecular Genetics and Metabolism Reports·2018· 13 citedOpen Access
Early feeding practices in infants with phenylketonuria across Europe
Molecular Genetics and Metabolism Reports·2018· 26 citedOpen Access

Frequent Co-authors

Anne Daly(12), Anita MacDonald(11), Rachel Skeath(10), Sharon Evans(10), Alex Pinto(9), Catherine Ashmore(9), Sandra Adams(7), Lisa Gaff(7), Louise Robertson(7), Charlotte Ellerton(7), Melanie Hill(6), Carolyn Dunlop(6), Heather Allen(6), Moira French(6), Anne Grimsley(6), Júlio César Rocha(6), Allyson Terry(6), Joanna Gribben(6), Lucy White(6), Barbara Cochrane(5)