(Q47685395)

4 February 2018

title

Brain phenylalanine concentration in the management of adults with phenylketonuria (English)

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4 February 2018

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R A Moats

1

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R Koch

2

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K Moseley

3

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P Guldberg

4

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F Guttler

5

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R G Boles

6

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M D Nelson

7

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publication date

1 February 2000

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4 February 2018

Journal of Inherited Metabolic Disease

published in

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4 February 2018

volume

23

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issue

1

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4 February 2018

page(s)

7-14

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https://scigraph.springernature.com/pub.10.1023/a:1005638627604

exact match

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cites work

Intelligence and quality of dietary treatment in phenylketonuria

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12 December 2020

Intellectual, neurologic, and neuropsychologic outcome in untreated subjects with nonphenylketonuria hyperphenylalaninemia. German Collaborative Study on Phenylketonuria.

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12 December 2020

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

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12 December 2020

Effect of age at loss of dietary control on intellectual performance and behavior of children with phenylketonuria

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12 December 2020

Identification and quantitation of phenylalanine in the brain of patients with phenylketonuria by means of localized in vivo 1H magnetic-resonance spectroscopy

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12 December 2020

Localized brain proton NMR spectroscopy in young adult phenylketonuria patients.

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12 December 2020

Treatment outcome of maternal phenylketonuria

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12 December 2020

In-vivo NMR spectroscopy in patients with phenylketonuria: changes of cerebral phenylalanine levels under dietary treatment

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12 December 2020

White matter abnormalities in phenylketonuria: results of magnetic resonance measurements.

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12 December 2020

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12 December 2020

In vivo NMR spectroscopy in patients with phenylketonuria: clinical significance of interindividual differences in brain phenylalanine concentrations.

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12 December 2020

Phenylketonuria: findings at MR imaging and localized in vivo H-1 MR spectroscopy of the brain in patients with early treatment.

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12 December 2020

Brain magnetic resonance imaging in children with optimally controlled hyperphenylalaninaemia

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12 December 2020

Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood

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12 December 2020

Magnetic resonance imaging of the brain in phenylketonuria

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12 December 2020

Brain MRI changes in phenylketonuria. Associations with dietary status.

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12 December 2020

Intellectual development of the patients of the German Collaborative Study of children treated for phenylketonuria

1 reference

12 December 2020

Phenylketonuria: MR imaging of the brain with clinical correlation.

1 reference

12 December 2020

Magnetic resonance imaging in phenylketonuria: reversal of cerebral white matter change

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12 December 2020

Intellectual development in 12-year-old children treated for phenylketonuria

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12 December 2020

Three methods of calibration in quantitative proton MR spectroscopy

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12 December 2020

Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria

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12 December 2020

Proton NMR observation of phenylalanine and an aromatic metabolite in the rabbit brain in vivo.

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12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1005638627604

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4 February 2018

Dimensions Publication ID

1040218050

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4 February 2018