Measurement of plasma amino acids by Ultraperformance® Liquid Chromatography.

Item

http://www.wikidata.org/entity/Q53086147

description

2011 nî lūn-bûn

@nan

2011年の論文

@ja

2011年学术文章

@wuu

2011年学术文章

@zh

2011年学术文章

@zh-cn

2011年学术文章

@zh-hans

2011年学术文章

@zh-my

2011年学术文章

@zh-sg

2011年學術文章

@yue

2011年學術文章

@zh-hant

name

Measurement of plasma amino acids by Ultraperformance® Liquid Chromatography.

@en

Measurement of plasma amino acids by Ultraperformance® Liquid Chromatography.

@nl

type

Item

label

Measurement of plasma amino acids by Ultraperformance® Liquid Chromatography.

@en

Measurement of plasma amino acids by Ultraperformance® Liquid Chromatography.

@nl

prefLabel

Measurement of plasma amino acids by Ultraperformance® Liquid Chromatography.

@en

Measurement of plasma amino acids by Ultraperformance® Liquid Chromatography.

@nl

P1476

Measurement of plasma amino acids by Ultraperformance® Liquid Chromatography.

@en

P2093

Gail Ditewig-Meyers

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

Kendon S Graham

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

Michael J Bennett

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

Robert Scott

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

Srinivas B Narayan

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

P2860

Newborn screening may fail to identify intermediate forms of maple syrup urine disease.

Reassessment of phenylalanine tolerance in adults with phenylketonuria is needed as body mass changes.

Validated quantitation of underivatized amino acids in human blood samples by volatile ion-pair reversed-phase liquid chromatography coupled to isotope dilution tandem mass spectrometry.

Analysis of plasma amino acids by HPLC with photodiode array and fluorescence detection.

Clinical and functional characterization of a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome.

A new reversed-phase liquid chromatographic/tandem mass spectrometric method for analysis of underivatised amino acids: evaluation for the diagnosis and the management of inherited disorders of amino acid metabolism.

Second-tier test for quantification of alloisoleucine and branched-chain amino acids in dried blood spots to improve newborn screening for maple syrup urine disease (MSUD).

Maple syrup urine disease: favourable effect of early diagnosis by newborn screening on the neonatal course of the disease.

P304

1177-1185

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

P31

scholarly article

P356

10.1515/CCLM.2011.200

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

P433

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

P478

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

P577

2011-07-01T00:00:00Z

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

P698

21722078

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