Adherence to clinic recommendations among patients with phenylketonuria in the United States-Reference-Cited by-同舟云学术

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Adherence to clinic recommendations among patients with phenylketonuria in the United States

Published:2017-03 Issue:3 Volume:120 Page:190-197
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Jurecki E.R.,Cederbaum S.,Kopesky J.,Perry K.,Rohr F.,Sanchez-Valle A.,Viau K.S.,Sheinin M.Y.,Cohen-Pfeffer J.L.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference21 articles.

1. How practical are recommendations for dietary control in phenylketonuria?;Walter;Lancet,2002

2. Phenylalanine hydroxylase deficiency: diagnosis and management guideline;Vockley;Genet. Med.,2014

3. Phenylketonuria: a review of current and future treatments;Al Hafid;Translat. Pediatr.,2015

4. Newborn screening 50years later: access issues faced by adults with PKU;Berry;Genet. Med.,2013

5. Management of phenylketonuria for optimal outcome: a review of guidelines for phenylketonuria management and a report of surveys of parents, patients, and clinic directors;Wappner;Pediatrics,1999

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1. Meta-analysis of bone mineral density in adults with phenylketonuria;Orphanet Journal of Rare Diseases;2024-09-12

2. Executive functions & metabolic control in phenylketonuria (PKU) and mild hyperphenylalaninemia (mHPA);Molecular Genetics and Metabolism;2024-09

3. Initial results from the PHEFREE longitudinal natural history study: Cross-sectional observations in a cohort of individuals with phenylalanine hydroxylase (PAH) deficiency;Molecular Genetics and Metabolism;2024-09

4. The challenge of adults with phenylketonuria who have been lost to care; a single center's attempt to reach those diagnosed with PKU over 60 years of newborn screening;Molecular Genetics and Metabolism Reports;2024-09

5. Patient and carer perceptions of video, telephone and in-person clinics for Phenylketonuria (PKU);Orphanet Journal of Rare Diseases;2024-08-20

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