(Q43934854)

28 November 2017

Prolidase deficiency diagnosed by 1H NMR spectroscopy of urine (English)

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28 November 2017

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6

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28 November 2017

S H Moolenaar

1

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28 November 2017

U F Engelke

2

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28 November 2017

N G Abeling

3

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28 November 2017

H Mandel

4

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28 November 2017

M Duran

5

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28 November 2017

1 December 2001

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Journal of Inherited Metabolic Disease

28 November 2017

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28 November 2017

24

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28 November 2017

843-850

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28 November 2017

8

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https://scigraph.springernature.com/pub.10.1023/a:1013940207973

28 November 2017

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cites work

In vivo and in vitro NMR spectroscopy reveal a putative novel inborn error involving polyol metabolism

1 reference

12 December 2020

Investigation of urea cycle enzyme disorders by 1H-NMR spectroscopy

1 reference

12 December 2020

Prolidase deficiency: a patient without hydroxyproline-containing iminodipeptides in urine

1 reference

12 December 2020

The use of liquid chromatography-mass spectrometry for the identification and quantification of urinary iminodipeptides in prolidase deficiency

1 reference

12 December 2020

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency studied using 2-dimensional proton nuclear magnetic resonance spectroscopy

1 reference

12 December 2020

Increased manganese content and reduced arginase activity in erythrocytes of a patient with prolidase deficiency (iminodipeptiduria)

1 reference

12 December 2020

Proton NMR spectroscopic analysis of multiple acyl-CoA dehydrogenase deficiency--capacity of the choline oxidation pathway for methylation in vivo

1 reference

12 December 2020

Clinical and biochemical characteristics of prolidase deficiency in siblings.

1 reference

12 December 2020

Analysis of biological fluids using 600 MHz proton NMR spectroscopy: Application of homonuclear two-dimensional J-resolved spectroscopy to urine and blood plasma for spectral simplification and assignment

1 reference

12 December 2020

Use of capillary zone electrophoresis for analysis of imidodipeptides in urine of prolidase-deficient patients

1 reference

12 December 2020

Prolidase deficiency: a multisystemic hereditary disorder

1 reference

12 December 2020

Further assignment of resonances in 1H NMR spectra of cerebrospinal fluid (CSF)

1 reference

12 December 2020

750 MHz 1H and 1H-13C NMR spectroscopy of human blood plasma

1 reference

12 December 2020

Isotachophoretic analysis of iminopeptides in the urine of patients with iminopeptiduria

1 reference

12 December 2020

A syndrome resembling lathyrism associated with iminodipeptiduria.

1 reference

12 December 2020

Measurement of iminodipeptides in the serum of patients with prolidase deficiency using liquid chromatography-mass spectrometry.

1 reference

12 December 2020

Prolidase deficiency among an Israeli population: prenatal diagnosis in a genetic disorder with uncertain prognosis

1 reference

12 December 2020

750 MHz 1H NMR spectroscopy characterisation of the complex metabolic pattern of urine from patients with inborn errors of metabolism: 2-hydroxyglutaric aciduria and maple syrup urine disease

1 reference

12 December 2020

1H-NMR spectroscopy of body fluids: inborn errors of purine and pyrimidine metabolism

1 reference

12 December 2020

Prolidase deficiency: detection of cases by a newborn urinary screening programme

1 reference

12 December 2020

NMR Spectroscopy of Biofluids

1 reference

Crossref

https://api.crossref.org/works/10.1023%2FA%3A1013940207973

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1023/A:1013940207973

1 reference

Dimensions Publication ID

28 November 2017

0 references

1 reference