(Q52260431)

English

Dihydrolipoyl dehydrogenase deficiency: a therapeutic trial with branched-chain amino acid restriction.

scientific article published in September 1986

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

Dihydrolipoyl dehydrogenase deficiency: a therapeutic trial with branched-chain amino acid restriction. (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

author name string

Y Sakaguchi

1

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

M Yoshino

2

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

S Aramaki

3

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

I Yoshida

4

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

F Yamashita

5

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

T Kuhara

6

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

I Matsumoto

7

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

T Hayashi

8

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

publication date

1 September 1986

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

145

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

4

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

271-274

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

https://scigraph.springernature.com/pub.10.1007/bf00439399

0 references

An inherited defect affecting the tricarboxylic acid cycle in a patient with congenital lactic acidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3769994

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A defect in pyruvate decarboxylase in a child with an intermittent movement disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/3769994

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Defect in Branched-Chain Amino Acid Metabolism in a Patient with Congenital Lactic Acidosis due to Dihydrolipoyl Dehydrogenase Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3769994

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of urinary organic acid profiles of a patient with dihydrolipoyl dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3769994

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lactic acidemia, neurologic deterioration and carbohydrate dependence in a girl with dihydrolipoyl dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3769994

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/3769994

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-performance liquid chromatographic determination of alpha-keto acids in human urine and plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/3769994

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/3769994

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purification of amine oxidase from beef plasma.

1 reference

https://pubmed.ncbi.nlm.nih.gov/3769994

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in Infancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/3769994

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00439399

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 April 2018

http://europepmc.org/abstract/MED/3769994

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