Reference health
Metabolic Control of Patients with Phenylketonuria in a Portuguese Metabolic Centre Comparing Three Different Recommendations
28/28 checkable references clean · checked 2026-07-22
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
2 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 28 checked references that resolve
resolves10.1186/s13023-017-0685-2
The complete European guidelines on phenylketonuria: diagnosis and treatment
resolves10.1007/8904_2017_60
The Use of d2 and Benton Tests for Assessment of Attention Deficits and Visual Memory in Teenagers with Phenylketonuria
resolves10.1186/s13023-015-0378-7
Special low protein foods for phenylketonuria: availability in Europe and an examination of their nutritional profile
resolves10.1038/ejcn.2016.54
Protein substitutes for phenylketonuria in Europe: access and nutritional composition
resolves10.1186/s13023-019-1011-y
Glycomacropeptide: long-term use and impact on blood phenylalanine, growth and nutritional status in children with PKU
resolves10.1186/s13023-021-01721-8
Continuous use of glycomacropeptide in the nutritional management of patients with phenylketonuria: a clinical perspective
resolves10.1038/ejcn.2017.38
Nutritional status in patients with phenylketonuria using glycomacropeptide as their major protein source
resolves10.1016/j.ymgme.2017.01.001
Adherence to clinic recommendations among patients with phenylketonuria in the United States
resolves10.1016/S0140-6736(02)09334-0
How practical are recommendations for dietary control in phenylketonuria?
resolves10.1016/j.ymgme.2019.04.004
International best practice for the evaluation of responsiveness to sapropterin dihydrochloride in patients with phenylketonuria
resolves10.1038/s41436-018-0403-z
Evidence- and consensus-based recommendations for the use of pegvaliase in adults with phenylketonuria
resolves10.1007/BF02312549
Diet termination in children with phenylketonuria: a review of psychological assessments used to determine outcome
resolves10.1016/j.ymgme.2007.05.006
Phenylalanine blood levels and clinical outcomes in phenylketonuria: A systematic literature review and meta-analysis
resolves10.1037/neu0000337
Cognitive outcomes in early-treated adults with phenylketonuria (PKU): A comprehensive picture across domains.
resolves10.1037/neu0000358
Cognitive profile and mental health in adult phenylketonuria: A PKU-COBESO study.
resolves10.1037/neu0000336
The impact of phenylalanine levels on cognitive outcomes in adults with phenylketonuria: Effects across tasks and developmental stages.
resolves10.1038/gim.2013.157
Phenylalanine hydroxylase deficiency: diagnosis and management guideline
resolves10.1515/jpem-2018-0527
The European Phenylketonuria Guidelines and the challenges on management practices in Portugal
resolves10.3390/nu12113440
Protein Labelling Accuracy for UK Patients with PKU Following a Low Protein Diet
resolves10.3390/nu13020707
Accidental Consumption of Aspartame in Phenylketonuria: Patient Experiences
resolves10.1016/j.ymgme.2013.08.013
Neurocognitive functioning in adults with phenylketonuria: Results of a long term study
resolves10.1212/WNL.0000000000011088
Phenylalanine Effects on Brain Function in Adult Phenylketonuria
resolves10.1007/s00415-019-09608-2
Neurological manifestations in adults with phenylketonuria: new cases and review of the literature
resolves10.1186/s13023-020-1343-7
Dried blood spot versus venous blood sampling for phenylalanine and tyrosine
The 2 references without a DOI — listed, not checked
no DOI — not checkedConsenso para o tratamento nutricional de fenilcetonúria (Article in Portuguese)
no DOI — not checkedJoint WHO/FAO/UNU Expert Consultation (2007). Protein and Amino Acid Requirements in Human Nutrition, World Health Organization.
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