Nutritional treatment for inborn errors of metabolism: indications, regulations, and availability of medical foods and dietary supplements using phenylketonuria as an example.
about
Advances in the nutritional and pharmacological management of phenylketonuriaRethinking the formulaInborn errors of metabolism identified via newborn screening: Ten-year incidence data and costs of nutritional interventions for research agenda planningThe Emerging Therapeutic Role of Medical Foods for Gastrointestinal Disorders.Expanding research to provide an evidence base for nutritional interventions for the management of inborn errors of metabolismEmerging issues in public health genomics.Insurance coverage of medical foods for treatment of inherited metabolic disorders.Table of Phenylalanine Content of Foods: Comparative Analysis of Data Compiled in Food Composition Tables.A critical reappraisal of dietary practices in methylmalonic acidemia raises concerns about the safety of medical foods. Part 1: isolated methylmalonic acidemias.Newborn screening 50 years later: access issues faced by adults with PKU.Development of the US English version of the phenylketonuria - quality of life (PKU-QOL) questionnaireSingle amino acid supplementation in aminoacidopathies: a systematic reviewThe role of evidence analysts in creating nutrition management guidelines for inherited metabolic disorders.Nutritional interventions in primary mitochondrial disorders: Developing an evidence base.Cost-effectiveness of liver transplantation in methylmalonic and propionic acidemias.Co-administration of creatine plus pyruvate prevents the effects of phenylalanine administration to female rats during pregnancy and lactation on enzymes activity of energy metabolism in cerebral cortex and hippocampus of the offspring.A questionnaire survey on the usage of low protein staple foods by people with phenylketonuria in Scotland.Impact of Dietary Intake on Bone Turnover in Patients with Phenylalanine Hydroxylase Deficiency.Healthy and sustainable diets for future generations.Strategies Used in Production of Phenylalanine-Free Foods for PKU Management
P2860
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P2860
Nutritional treatment for inborn errors of metabolism: indications, regulations, and availability of medical foods and dietary supplements using phenylketonuria as an example.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Nutritional treatment for inbo ...... phenylketonuria as an example.
@ast
Nutritional treatment for inbo ...... phenylketonuria as an example.
@en
type
label
Nutritional treatment for inbo ...... phenylketonuria as an example.
@ast
Nutritional treatment for inbo ...... phenylketonuria as an example.
@en
prefLabel
Nutritional treatment for inbo ...... phenylketonuria as an example.
@ast
Nutritional treatment for inbo ...... phenylketonuria as an example.
@en
P2093
P2860
P1476
Nutritional treatment for inbo ...... phenylketonuria as an example.
@en
P2093
Kathleen L Huntington
Kathryn M Camp
Michele A Lloyd-Puryear
P2860
P356
10.1016/J.YMGME.2012.07.005
P577
2012-07-16T00:00:00Z