Main issues in micronutrient supplementation in phenylketonuria-Reference-Cited by-同舟云学术

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Main issues in micronutrient supplementation in phenylketonuria

Published:2013 Issue: Volume:110 Page:S1-S5
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Lammardo A.M.,Robert M.,Rocha J.C.,van Rijn M.,Ahring K.,Bélanger-Quintana A.,MacDonald A.,Dokoupil K.,Ozel H. Gokmen,Goyens P.,Feillet F.

Publisher

Elsevier BV

Subject

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

Reference34 articles.

1. Micronutrients in health and disease;Shenkin;Postgrad. Med. J.,2006

2. Dietary management practices in phenylketonuria across European centres;Ahring;Clin. Nutr.,2009

3. Free use of fruits and vegetables in phenylketonuria;MacDonald;J. Inherit. Metab. Dis.,2003

4. Unrestricted consumption of fruits and vegetables in phenylketonuria: no major impact on metabolic control;Rohde;Eur. J. Clin. Nutr.,2012

5. Positive effect of a simplified diet on blood phenylalanine control in different phenylketonuria variants, characterized by newborn BH4 loading test and PAH analysis;Zimmermann;Mol. Genet. Metab.,2012

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1. Potential Micronutrient Deficiencies in the First 1000 Days of Life: The Pediatrician on the Side of the Weakest;Current Obesity Reports;2024-03-21

2. Micronutrient Deficiency in Inherited Metabolic Disorders Requiring Diet Regimen: A Brief Critical Review;International Journal of Molecular Sciences;2023-11-30

3. Food or medicine? A European regulatory perspective on nutritional therapy products to treat inborn errors of metabolism;Journal of Inherited Metabolic Disease;2023-09-13

4. Clinical, genetic, and experimental research of hyperphenylalaninemia;Frontiers in Genetics;2023-01-04

5. Inborn errors of metabolism: Nutrition management of phenylketonuria;Encyclopedia of Human Nutrition;2023

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