(Q43236062)

16 November 2017

title

Prolidase deficiency: it looks like systemic lupus erythematosus but it is not. (English)

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systemic lupus erythematosus

16 November 2017

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Aharon Klar

1

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16 November 2017

Paulina Navon-Elkan

2

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16 November 2017

Alan Rubinow

3

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16 November 2017

David Branski

4

1 reference

16 November 2017

Haggit Hurvitz

5

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16 November 2017

Ernst Christensen

6

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16 November 2017

Morad Khayat

7

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16 November 2017

Tzipora C Falik-Zaccai

8

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16 November 2017

publication date

24 November 2009

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European Journal of Pediatrics

16 November 2017

published in

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16 November 2017

volume

169

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16 November 2017

issue

6

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16 November 2017

page(s)

727-732

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https://scigraph.springernature.com/pub.10.1007/s00431-009-1102-1

16 November 2017

exact match

0 references

cites work

Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiency

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00431-009-1102-1

Determination of dipeptides in urine

21 January 2018

1 reference

12 December 2020

Prolidase deficiency and the biochemical assays used in its diagnosis

1 reference

12 December 2020

Topical treatment of skin ulcers in prolidase deficiency.

1 reference

12 December 2020

Systemic lupus erythematosus-like disease in a 6-year-old boy with prolidase deficiency

1 reference

12 December 2020

A nonsense mutation of PEPD in four Amish children with prolidase deficiency

1 reference

12 December 2020

Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations

1 reference

12 December 2020

Prolidase deficiency: a multisystemic hereditary disorder

1 reference

12 December 2020

A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndrome.

1 reference

12 December 2020

Prolidase deficiency and systemic lupus erythematosus

1 reference

12 December 2020

Structural and functional evaluation of modifications in the composite skin graft: cryopreserved dermis and cultured keratinocytes

1 reference

12 December 2020

Clinical approach to cutaneous vasculitis

1 reference

12 December 2020

Iminodipeptiduria: a genetic defect in recycling collagen; a method for determining prolidase in erythrocytes

1 reference

12 December 2020

Formiminoglutamic aciduria in a slightly retarded boy with chronic obstructive lung disease.

1 reference

12 December 2020

1 reference

12 December 2020

A prolidase deficiency in man with iminopeptiduria

1 reference

12 December 2020

The 1982 revised criteria for the classification of systemic lupus erythematosus

1 reference

12 December 2020

Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family.

1 reference

12 December 2020

Improved assay of glutaryl-CoA dehydrogenase in cultured cells and liver: application to glutaric aciduria type I

1 reference

12 December 2020

A syndrome resembling lathyrism associated with iminodipeptiduria

1 reference

12 December 2020

Prolidase deficiency with hyperimmunoglobulin E: a case report

1 reference

12 December 2020

Skin capillary abnormalities as indicators of organ involvement in scleroderma (systemic sclerosis), Raynaud's syndrome and dermatomyositis

1 reference

12 December 2020

A broad spectrum of developmental delay in a large cohort of prolidase deficiency patients demonstrates marked interfamilial and intrafamilial phenotypic variability

1 reference

12 December 2020

Prolidase and prolidase deficiency

1 reference

12 December 2020

10.1007/S00431-009-1102-1

Identifiers

DOI

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16 November 2017

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