Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations.

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Sapropterin dihydrochloride for phenylketonuria Sapropterin dihydrochloride for phenylketonuria Sapropterin dihydrochloride for phenylketonuria Novel pharmacological chaperones that correct phenylketonuria in mice.Biopterin responsive phenylalanine hydroxylase deficiency.

P2860

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P2860

Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations.

Item

http://www.wikidata.org/entity/Q44099354

description

2002 nî lūn-bûn

@nan

2002年の論文

@ja

2002年学术文章

@wuu

2002年学术文章

@zh

2002年学术文章

@zh-cn

2002年学术文章

@zh-hans

2002年学术文章

@zh-my

2002年学术文章

@zh-sg

2002年學術文章

@yue

2002年學術文章

@zh-hant

name

Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations.

@en

Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations.

@nl

type

Item

label

Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations.

@en

Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations.

@nl

prefLabel

Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations.

@en

Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations.

@nl

P1476

Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations

@en

P2093

Johannes Zschocke

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

Kurt Ullrich

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

Martin Lindner

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

Robert Steinfeld

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

Zoltan Lukacs

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

P2860

A structural hypothesis for BH4 responsiveness in patients with mild forms of hyperphenylalaninaemia and phenylketonuria.

A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype.

Human phenylalanine hydroxylase mutations and hyperphenylalaninemia phenotypes: a metanalysis of genotype-phenotype correlations.

Tetrahydrobiopterin responsiveness in phenylketonuria differs between patients with the same genotype.

Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Dutch neonates.

P2888

s00431-002-0966-0

P304

403-405

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

P31

scholarly article

P356

10.1007/S00431-002-0966-0

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

P433

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

P478

161

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

P50

Alfried Kohlschütter

P577

2002-07-01T00:00:00Z

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

P698

12174822

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

P921

phenylketonuria

Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations.

about

P2860

P2860

Tetrahydrobiopterin monotherapy for phenylketonuria patients with common mild mutations.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P921