Reference health

Implementing a Transition Program from Paediatric to Adult Services in Phenylketonuria: Results after Two Years of Follow-Up with an Adult Team

https://doi.org/10.3390/nu13030799
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35/35 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.

8 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 35 checked references that resolve
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Phenylketonuria
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Phenylketonuria, co‐morbidity, and ageing: A review
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Neuropsychiatric comorbidities in adults with phenylketonuria: A retrospective cohort study
resolves10.1080/87565641.2016.1243109
Systematic Review and Meta-Analysis of Neuropsychiatric Symptoms and Executive Functioning in Adults With Phenylketonuria
resolves10.1002/jimd.12065
The neurological and psychological phenotype of adult patients with early‐treated phenylketonuria: A systematic review
resolves10.1016/j.ymgme.2018.09.006
Prevalence of comorbid conditions among adult patients diagnosed with phenylketonuria
resolves10.1016/j.ymgme.2010.05.017
Suboptimal outcomes in patients with PKU treated early with diet alone: Revisiting the evidence
resolves10.1186/s13023-019-1153-y
Clinical burden of illness in patients with phenylketonuria (PKU) and associated comorbidities - a retrospective study of German health insurance claims data
resolves10.1007/s10545-005-4478-8
Living with phenylketonuria: Perspectives of patients and their families
resolves10.1007/s10545-010-9073-y
The reality of dietary compliance in the management of phenylketonuria
resolves10.1159/000342256
Adherence Issues in Inherited Metabolic Disorders Treated by Low Natural Protein Diets
resolves10.1515/IJAMH.2004.16.1.41
Blood phenylalanine control in adolescents with phenylketonuria
resolves10.1038/ejcn.2010.258
Blood phenylalanine control in phenylketonuria: a survey of 10 European centres
resolves10.1016/S0140-6736(02)09334-0
How practical are recommendations for dietary control in phenylketonuria?
resolves10.1007/s00431-014-2458-4
Management of adult patients with phenylketonuria: survey results from 24 countries
resolves10.1016/j.ymgme.2017.01.001
Adherence to clinic recommendations among patients with phenylketonuria in the United States
resolves10.1038/gim.2013.10
Newborn screening 50 years later: access issues faced by adults with PKU
resolves10.1016/j.ejmg.2019.103818
Adult patient perspectives on phenylketonuria care: Highlighting the need for dedicated adult management and services
resolves10.1016/j.ymgme.2009.09.005
Management of phenylketonuria in Europe: Survey results from 19 countries
resolves10.1016/j.ymgme.2010.06.006
Reaching out to the lost generation of adults with early-treated phenylketonuria (PKU)
resolves10.1016/j.arcped.2018.05.009
Transition from pediatric to adult care in adolescents with hereditary metabolic diseases: Specific guidelines from the French network for rare inherited metabolic diseases (G2M)
resolves10.1016/j.ymgme.2009.10.182
Psychiatric symptoms and disorders in phenylketonuria☆
resolves10.7861/clinmed.2019-0077
Facilitating transition of young people with long-term health conditions from children’s to adults’ healthcare services – implications of a 5-year research programme
resolves10.1186/s13023-020-01391-y
PKU dietary handbook to accompany PKU guidelines
resolves10.1080/21678707.2018.1536541
Treatment options and dietary supplements for patients with phenylketonuria
resolves10.1007/s10545-011-9284-x
Transition of young adults with phenylketonuria from pediatric to adult care
resolves10.1186/s13023-016-0410-6
Ten years of specialized adult care for phenylketonuria – a single-centre experience
resolves10.1111/j.1365-2265.2008.03467.x
Transition process of patients with type 1 diabetes (T1DM) from paediatric to the adult health care service: a hospital‐based approach
resolves10.14423/SMJ.0000000000000950
Lessons Learned from Building a Pediatric-to-Adult Sickle Cell Transition Program
resolves10.1017/S0007114511000298
Adjusting diet with sapropterin in phenylketonuria: what factors should be considered?
resolves10.1111/j.1651-2227.1995.tb13748.x
Nutrient intake and food consumption of adolescents and young adults with phenylketonuria
resolves10.1136/adc.2010.202473
Improving the transition between paediatric and adult healthcare: a systematic review
resolves10.1016/1054-139X(95)00077-6
Between two worlds: Bridging the cultures of child health and adult medicine
resolves10.1016/j.jada.2009.10.030
Perspectives on Dietary Adherence among Women with Inborn Errors of Metabolism
resolves10.1007/s00431-010-1364-7
Transition from pediatric to adult health care: expectations of adolescents with chronic disorders and their parents
The 8 references without a DOI — listed, not checked
no DOI — not checkedThe complete European guidelines on phenylketonuria: Diagnosis and treatment
no DOI — not checkedNutritional management of phenylketonuria
no DOI — not checkedAdult issues in phenylketonuria
no DOI — not checkedPhenylketonuria: A review of current and future treatments
no DOI — not checkedConsensus for the nutritional treatment of phenylketonuria
no DOI — not checkedMetabolic control in patients with phenylketonuria pre- and post-sapropterin loading test
no DOI — not checkedTransition in a paediatric rheumatology unit—experience from a tertiary unit
no DOI — not checkedPhenylketonuria (PKU): A problem solved?
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