Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

about

Translation of Nutritional Genomics into Nutrition Practice: The Next Step Parkinsonism in Inherited Metabolic Disorders: Key Considerations and Major Features

P2860

Q33365157-83A95D14-2C0B-4C03-9DB0-9496CD65F59C Q58122613-3568E8D5-5F5F-44BC-AB32-D4F9F365D619

P2860

Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

Item

http://www.wikidata.org/entity/Q35889337

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

@zh

2015年论文

@zh-cn

name

Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

@ast

Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

@en

type

Item

label

Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

@ast

Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

@en

prefLabel

Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

@ast

Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

@en

P1476

Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

@en

P2093

Lindsay C Burrage

http://www.w3.org/2001/XMLSchema#string

Lisa J Barclay

http://www.w3.org/2001/XMLSchema#string

Suzanne W Boyer

http://www.w3.org/2001/XMLSchema#string

P2860

Improved nutritional management of phenylketonuria by using a diet containing glycomacropeptide compared with amino acids

Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia

Nutrition management guideline for maple syrup urine disease: an evidence- and consensus-based approach.

Neuropsychological outcome of subjects participating in the PKU adult collaborative study: a preliminary review.

Long-term management of patients with urea cycle disorders.

The discovery of phenylketonuria: the story of a young couple, two retarded children, and a scientist.

Behaviour in early treated phenylketonuria: a systematic review.

Sodium phenylbutyrate decreases plasma branched-chain amino acids in patients with urea cycle disorders.

Recommendations for the use of sapropterin in phenylketonuria.

Effect of dietary interventions in the maintenance of normoglycaemia in glycogen storage disease type 1a: a systematic review and meta-analysis.

P304

502-510

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1177/0884533615586201

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2015-06-16T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

26079521

http://www.w3.org/2001/XMLSchema#string

P921

nutrition disorder

P932

4515158

http://www.w3.org/2001/XMLSchema#string

Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

about

P2860

P2860

Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921

P932