(Q43592447)

25 November 2017

title

Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative Study (English)

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25 November 2017

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maternal phenylketonuria

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based on heuristic

inferred from title

congenital heart disease

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Levy HL

1

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25 November 2017

Guldberg P

2

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25 November 2017

Güttler F

3

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25 November 2017

Hanley WB

4

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25 November 2017

Matalon R

5

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25 November 2017

Rouse BM

6

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25 November 2017

Trefz F

7

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25 November 2017

Azen C

8

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25 November 2017

Allred EN

9

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25 November 2017

de la Cruz F

10

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25 November 2017

Koch R

11

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25 November 2017

language of work or name

English

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publication date

1 May 2001

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25 November 2017

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25 November 2017

volume

49

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25 November 2017

issue

5

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25 November 2017

page(s)

636-642

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https://scigraph.springernature.com/pub.10.1203/00006450-200105000-00005

25 November 2017

exact match

0 references

cites work

Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

Cardiac defects in the children of mothers with high concentrations of plasma phenylalanine

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

PAH Mutation Analysis Consortium Database: 1997. Prototype for relational locus-specific mutation databases

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

A preliminary report of the collaborative study of maternal phenylketonuria in the United States and Canada.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

The International Collaborative Study on maternal phenylketonuria: organization, study design and description of the sample.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

Fetal ultrasonography in maternal PKU.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

Prevalence and clinical significance of cardiac murmurs in neonates

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

Cardiovascular defects among the progeny of mouse phenylketonuria females.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

Molecular pathways controlling heart development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

Homeodomain factor Nkx2-5 controls left/right asymmetric expression of bHLH gene eHand during murine heart development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

NK-2 homeobox genes and heart development

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

Heart and extra-embryonic mesodermal defects in mouse embryos lacking the bHLH transcription factor Hand1

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

Congenital heart disease caused by mutations in the transcription factor NKX2-5

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

Histidinaemia. Part I: Reconciling retrospective and prospective findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200105000-00005

10.1203/00006450-200105000-00005

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

25 November 2017

1026646746

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