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reality of dietary compliance in the management of phenylketonuria

Journal of inherited metabolic disease, 2010-12, Vol.33 (6), p.665-670

2010

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Do Thickening Agents Used in Dysphagia Diet Affect Drug Bioavailability?

European journal of pharmaceutical sciences, 2022-07, Vol.174, p.106197-106197, Article 106197

2022

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Weight Management in Phenylketonuria: What Should Be Monitored?

Annals of nutrition and metabolism, 2016-01, Vol.68 (1), p.60-65

2016

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Dietary management practices in phenylketonuria across European centres

Clinical nutrition (Edinburgh, Scotland), 2009-06, Vol.28 (3), p.231-236

2009

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Successful management of rhabdomyolysis with triheptanoin in a child with severe long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency

Neuromuscular disorders : NMD, 2023-04, Vol.33 (4), p.315-318

2023

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When should social service referral be considered in phenylketonuria?

Molecular genetics and metabolism reports, 2015-03, Vol.2 (C), p.85-88

2015

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The association of milk and multiple food avoidance with growth parameters in infants and children

Annals of allergy, asthma, & immunology, 2024-06, Vol.132 (6), p.745-751.e2

2024

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Erratum to "Recommendations on phenylketonuria in Turkey" [Turk J Pediatr 2022; 64: 413-434]

Turkish journal of pediatrics, 2022-11, Vol.64 (6), p.1175-1175

2022

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Special low protein foods for phenylketonuria: availability in Europe and an examination of their nutritional profile

Orphanet journal of rare diseases, 2015-12, Vol.10 (163), p.162-162, Article 162

2015

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Effects of a Psychobiotic Supplement on Serum Brain-derived Neurotrophic Factor Levels in Depressive Patients: A Post Hoc Analysis of a Randomized Clinical Trial

Journal of neurogastroenterology and motility, 2020-10, Vol.26 (4), p.486-495

2020

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Protein Substitute Requirements of Patients with Phenylketonuria on BH4 Treatment: A Systematic Review and Meta-Analysis

Nutrients, 2021-03, Vol.13 (3), p.1040

2021

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Optimising growth in phenylketonuria: Current state of the clinical evidence base

Clinical nutrition (Edinburgh, Scotland), 2012-02, Vol.31 (1), p.16-21

2012

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Nutritional content of modular feeds: how accurate is feed production?

Archives of disease in childhood, 2013-03, Vol.98 (3), p.184-188

2013

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Long-Term Growth in Phenylketonuria: A Systematic Review and Meta-Analysis

Nutrients, 2019-09, Vol.11 (9), p.2070

2019

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Errors in emergency feeds in inherited metabolic disorders: a randomised controlled trial of three preparation methods

Archives of disease in childhood, 2010-10, Vol.95 (10), p.776-780

2010

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Adjusting diet with sapropterin in phenylketonuria: what factors should be considered?

British journal of nutrition, 2011-07, Vol.106 (2), p.175-182

2011

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Does a lower carbohydrate protein substitute impact on blood phenylalanine control, growth and appetite in children with PKU?

Molecular genetics and metabolism, 2011, Vol.104, p.S64-S67

2011

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Changing dietary practices in phenylketonuria

Turkish journal of pediatrics, 2009-09, Vol.51 (5), p.409-415

2009

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Development of a practical dietitian road map for the nutritional management of phenylketonuria (PKU) patients on pegvaliase

Molecular genetics and metabolism reports, 2021-09, Vol.28, p.100771, Article 100771

2021

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Home visits in phenylketonuria: a 12-month longitudinal study

Turkish journal of pediatrics, 2011-03, Vol.53 (2), p.149-153

2011

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Recommendations on phenylketonuria in Turkey

The Turkish journal of pediatrics, 2022, Vol.64 (3), p.413-434

2022

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Successful management of rhabdomyolysis with triheptanoin in a child with severe long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency

Neuromuscular disorders : NMD, 2023, Vol.33 (4), p.315-318

2023

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A New Concept in the Nutrition Therapy of Childhood Obesity: Food Insulin Index

Güncel pediatri, 2018-08, Vol.16 (2), p.205-218

2018

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Longitudinal Dietary Intake Data in Patients with Phenylketonuria from Europe: The Impact of Age and Phenylketonuria Severity

reality of dietary compliance in the management of phenylketonuria

Do Thickening Agents Used in Dysphagia Diet Affect Drug Bioavailability?

Weight Management in Phenylketonuria: What Should Be Monitored?

Dietary management practices in phenylketonuria across European centres

Successful management of rhabdomyolysis with triheptanoin in a child with severe long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency

When should social service referral be considered in phenylketonuria?

The association of milk and multiple food avoidance with growth parameters in infants and children

Erratum to "Recommendations on phenylketonuria in Turkey" [Turk J Pediatr 2022; 64: 413-434]

Special low protein foods for phenylketonuria: availability in Europe and an examination of their nutritional profile

Effects of a Psychobiotic Supplement on Serum Brain-derived Neurotrophic Factor Levels in Depressive Patients: A Post Hoc Analysis of a Randomized Clinical Trial

Protein Substitute Requirements of Patients with Phenylketonuria on BH4 Treatment: A Systematic Review and Meta-Analysis

Optimising growth in phenylketonuria: Current state of the clinical evidence base

Nutritional content of modular feeds: how accurate is feed production?

Long-Term Growth in Phenylketonuria: A Systematic Review and Meta-Analysis

Errors in emergency feeds in inherited metabolic disorders: a randomised controlled trial of three preparation methods

Adjusting diet with sapropterin in phenylketonuria: what factors should be considered?

Blood Phenylalanine Levels in Patients with Phenylketonuria from Europe between 2012 and 2018: Is It a Changing Landscape?

Does a lower carbohydrate protein substitute impact on blood phenylalanine control, growth and appetite in children with PKU?

Changing dietary practices in phenylketonuria

Development of a practical dietitian road map for the nutritional management of phenylketonuria (PKU) patients on pegvaliase

Home visits in phenylketonuria: a 12-month longitudinal study

Recommendations on phenylketonuria in Turkey

Successful management of rhabdomyolysis with triheptanoin in a child with severe long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency

A New Concept in the Nutrition Therapy of Childhood Obesity: Food Insulin Index

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