(Q64913458)

30 June 2019

title

Prenatal exclusion of primary hyperoxaluria type 1. (English)

1 reference

30 June 2019

main subject

primary hyperoxaluria

1 reference

C J Danpure

1

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30 June 2019

P R Jennings

2

1 reference

30 June 2019

R J Penketh

3

1 reference

30 June 2019

P J Wise

4

1 reference

30 June 2019

C H Rodeck

5

1 reference

30 June 2019

language of work or name

English

0 references

publication date

1 February 1988

1 reference

30 June 2019

published in

The Lancet

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30 June 2019

volume

1

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30 June 2019

issue

8581

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30 June 2019

page(s)

367

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30 June 2019

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2888%2991171-3

7 January 2021

Peroxisomal alanine:glyoxylate aminotransferase and prenatal diagnosis of primary hyperoxaluria type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2888%2991171-3

7 January 2021

Fetal liver biopsy for prenatal diagnosis of ornithine carbamyl transferase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2888%2991171-3

7 January 2021

Enzymological diagnosis of primary hyperoxaluria type 1 by measurement of hepatic alanine: glyoxylate aminotransferase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2888%2991171-3

7 January 2021

A new micro-assay for human liver alanine: glyoxylate aminotransferase

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2888%2991171-3

7 January 2021

Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2888%2991171-3

7 January 2021

10.1016/S0140-6736(88)91171-3

Identifiers

DOI

1 reference

30 June 2019

PubMed ID

2893183

1 reference

30 June 2019