(Q43535851)

24 November 2017

beta-Ketothiolase deficiency with favourable evolution (English)

1 reference

beta-ketothiolase deficiency

24 November 2017

1 reference

G Sabetta

1

1 reference

24 November 2017

C Bachmann

2

1 reference

24 November 2017

O Giardini

3

1 reference

24 November 2017

M Castro

4

1 reference

24 November 2017

M Gambarara

5

1 reference

24 November 2017

C D Vici

6

1 reference

24 November 2017

K Bartlett

7

1 reference

24 November 2017

B Middleton

8

1 reference

24 November 2017

1 January 1987

1 reference

Journal of Inherited Metabolic Disease

24 November 2017

1 reference

24 November 2017

10

1 reference

24 November 2017

4

1 reference

24 November 2017

405-406

1 reference

https://scigraph.springernature.com/pub.10.1007/bf01799988

24 November 2017

0 references

cites work

An inherited disorder of isoleucine catabolism causing accumulation of alpha-methylacetoacetate and alpha-methyl-beta -hydroxybutyrate, and intermittent metabolic acidosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3126364

PubMed

reference URL

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The synthesis and characterisation of 2-methylacetoacetyl coenzyme A and its use in the identification of the site of the defect in 2-methylacetoacetic and 2-methyl-3-hydroxybutyric aciduria

1 reference

https://pubmed.ncbi.nlm.nih.gov/3126364

PubMed

reference URL

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Organic acids in urine: sample preparation for GC/MS

1 reference

https://pubmed.ncbi.nlm.nih.gov/3126364

PubMed

reference URL

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/BF01799988

1 reference

Dimensions Publication ID

24 November 2017

0 references

1 reference