Anne Daly

Birmingham Women's Hospital — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

26h-index2.1kcitations146works1.02yr avg
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Research Topics

Metabolism and Genetic Disorders(107), Diet and metabolism studies(82), Amino Acid Enzymes and Metabolism(26), Muscle metabolism and nutrition(21), Child Nutrition and Feeding Issues(20)

Publications146 total

From Control to Optimisation: Evolving Strategies in the Nutritional Management of Inborn Errors of Protein Metabolism
Journal of Inherited Metabolic Disease·2025Open Access
Point-of-Care Testing in PKU: A New ERA of Blood Phenylalanine Monitoring
Nutrients·2025· 1 citedOpen Access
Navigating Adolescence with PKU: Adherence, Metabolic Control, and Wellbeing in a UK Clinical Centre
Nutrients·2025Open Access
Improving sapropterin administration efficacy in PKU: Clinical practice case studies
Molecular Genetics and Metabolism Reports·2025Open Access
Protein Substitute Absorption: A Randomised Controlled Trial Comparing CGMP vs. Amino Acids vs. Micellar Casein in Healthy Volunteers
Nutrients·2025· 1 citedOpen Access
Global Clinical Practice in Transitioning Protein Substitutes for Children with Phenylketonuria
Nutrients·2025· 1 citedOpen Access
Nutritional profiling of foods for Phenylketonuria
Scientific Reports·2025· 2 citedOpen Access
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
Transitioning of protein substitutes in patients with phenylketonuria: a pilot study
Frontiers in Nutrition·2025· 3 citedOpen Access
UK Patient Access to Low-Protein Prescription Foods in Phenylketonuria (PKU): An Uneasy Path
Nutrients·2025· 1 citedOpen Access
P283: A prolonged-release formula has a positive impact on morning phenylalanine and tyrosine fluctuations in patients with classical phenylketonuria (PKU)
Genetics in Medicine Open·2025Open Access
Management of phenylketonuria in three European countries: analysis of patient characteristics, health service use and adherence to treatment guidelines
SSRN Electronic Journal·2025Open Access
A technology-enabled collaborative learning model (Project ECHO) to upskill primary care providers in best practice pain care
Australian Journal of Primary Health·2024· 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
Longitudinal Dietary Intake Data in Patients with Phenylketonuria from Europe: The Impact of Age and Phenylketonuria Severity
Nutrients·2024· 1 citedOpen Access
Outcomes of Pediatric Liver Transplantation in Glycogen Storage Disease Type 1b—A Single‐Center Experience
Pediatric Transplantation·2024· 2 cited
Patient and carer perceptions of video, telephone and in-person clinics for Phenylketonuria (PKU)
Orphanet Journal of Rare Diseases·2024· 2 citedOpen Access
A 12-month, longitudinal, intervention study examining a tablet protein substitute preparation in the management of tyrosinemia
Molecular Genetics and Metabolism Reports·2024· 1 citedOpen Access
Phenylalanine-Free Infant Formula in Patients with Phenylketonuria: A Retrospective Study
Nutrients·2024· 2 citedOpen Access
Blood Phenylalanine Levels in Patients with Phenylketonuria from Europe between 2012 and 2018: Is It a Changing Landscape?
Nutrients·2024· 9 citedOpen Access
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Frequent Co-authors

Anita MacDonald(46), Sharon Evans(34), Alex Pinto(18), Júlio César Rocha(14), Catherine Ashmore(14), Marjorie Dixon(8), Allyson Terry(8), Joanna Gribben(7), Louise Robertson(7), F. White(7), S. Chahal(7), Anupam Chakrapani(7), U. Meyer(6), J. Wildgoose(6), P.H. O'Connor Davies(6), Barbara Cochrane(6), Lucy White(6), Francjan J. van Spronsen(5), Christian J. Hendriksz(5), Manuela Almeida(5)