(Q52097025)

English

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

scientific article published in January 1983

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scholarly article

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

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

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

1 reference

based on heuristic

inferred from title

author name string

S K Wadman

1

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

M Duran

2

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

F A Beemer

3

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

B P Cats

4

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

J L Johnson

5

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

K V Rajagopalan

6

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

J M Saudubray

7

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

H Ogier

8

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

C Charpentier

9

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

R Berger

10

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

publication date

1 January 1983

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

6 Suppl 1

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

78-83

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

https://scigraph.springernature.com/pub.10.1007/bf01811328

0 references

Urinary Purines in a Patient with a Severely Defective T Cell Immunity and a Purine Nucleoside Phosphorylase Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6413778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6413778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6413778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural and metabolic relationship between the molybdenum cofactor and urothione

1 reference

https://pubmed.ncbi.nlm.nih.gov/6413778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of the molybdenum cofactor of sulfite oxidase, xanthine, oxidase, and nitrate reductase. Identification of a pteridine as a structural component

1 reference

https://pubmed.ncbi.nlm.nih.gov/6413778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microassay of inorganic sulfate in biological fluids by controlled flow anion chromatography

1 reference

https://pubmed.ncbi.nlm.nih.gov/6413778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple screening test for sulfite oxidase deficiency: Detection of urinary thiosulfate by a modification of sörbo's method

1 reference

https://pubmed.ncbi.nlm.nih.gov/6413778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amino acid intolerance during prolonged total parenteral nutrition reversed by molybdate therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/6413778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6413778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6413778

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01811328

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6413778

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