(Q68012640)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3215199%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

title

Report on a new patient with combined deficiencies of sulphite oxidase and xanthine dehydrogenase due to molybdenum cofactor deficiency (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3215199%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

1 reference

molybdenum cofactor deficiency

1 reference

W Endres

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3215199%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

Y S Shin

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3215199%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

R Günther

3

1 reference

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20 September 2019

H Ibel

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3215199%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

M Duran

5

1 reference

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20 September 2019

S K Wadman

6

1 reference

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20 September 2019

publication date

1 December 1988

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3215199%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Pediatrics

20 September 2019

published in

1 reference

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20 September 2019

volume

148

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20 September 2019

issue

3

1 reference

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20 September 2019

page(s)

246-249

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00441412

20 September 2019

exact match

0 references

cites work

[Double deficiency of sulfite and xanthine oxidase causing encephalopathy and due to a hereditary anomaly in the metabolism of molybdenum]

1 reference

12 December 2020

Neuropathologic changes in a case of sulfite oxidase deficiency

1 reference

12 December 2020

Effects of Taurine, Glycine and GABA on Convulsions Produced by Strychnine in the Rabbit

1 reference

12 December 2020

The neuropharmacology of taurine

1 reference

12 December 2020

Sulfite oxidase deficiency. Biochemical and clinical investigations of a hereditary metabolic disorder in sulfur metabolism

1 reference

12 December 2020

Absence of hepatic molybdenum cofactor: an inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase.

1 reference

12 December 2020

Combined deficiency of xanthine oxidase and sulphite oxidase: A defect of molybdenum metabolism or transport?

1 reference

12 December 2020

The toxicity of sulphite. I. Long-term feeding and multigeneration studies in rats

1 reference

12 December 2020

Neuropathological findings in a case of combined deficiency of sulphite oxidase and xanthine dehydrogenase

1 reference

12 December 2020

Hereditary xanthinuria: report on three patients and short review of the literature

1 reference

12 December 2020

Renal excretion of cystathionine and creatinine in humans at different ages

1 reference

12 December 2020

Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00441412

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3215199%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

1 reference