(Q48900141)

English

Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. I. Clinical, metabolical, and biochemical findings.

scientific article published in September 1982

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scholarly article

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two brothers. I. Clinical, metabolical, and biochemical findings. (English)

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

dehydrogenation

1 reference

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inferred from title

Glutaric aciduria

1 reference

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author name string

W Lehnert

1

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

U Wendel

2

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

S Lindenmaier

3

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

N Böhm

4

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

publication date

1 September 1982

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

European Journal of Pediatrics

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

139

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Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

56-59

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Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

1

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

https://scigraph.springernature.com/pub.10.1007/bf00442081

0 references

A new membrane iron-sulfur flavoprotein of the mitochondrial electron transfer system the entrance point of the fatty acyl dehydrogenation pathway?

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent Hypoglycemia Associated with Glutaric Aciduria Type II in an Adult

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein katabolism and oxygen consumption during starvation in infants, young adults and old men

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

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CARBOHYDRATE RESERVES IN THE NEWBORN INFANT

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

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Glutaric aciduria type II: in vitro studies on substrate oxidation, acyl-CoA dehydrogenases, and electron-transferring flavoprotein in cultured skin fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glutaric aciduria Type II

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical studies in a patient with defects in the metabolism of acyl‐CoA and sarcosine: Another possible case of glutaric aciduria type II

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Excretion of 2-methyl-3-oxovaleric acid in propionic acidemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

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Ethylmalonic-adipic aciduria. In vivo and in vitro studies indicating deficiency of activities of multiple acyl-CoA dehydrogenases

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid diagnosis of maple syrup urine disease (branched chain ketoaciduria) by micro-enzyme assay in leukocytes and fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new iron-sulfur flavoprotein of the respiratory chain. A component of the fatty acid beta oxidation pathway

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal detection of defects in propionate metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isovaleric acidemia: a new genetic defect of leucine metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glutaric aciduria type II: Report on a previously undescribed metabolic disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/7173259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00442081

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/7173259

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