(Q39222719)

10 September 2017

title

Methylmalonyl-CoA mutase deficiency associated with severe neonatal hyperammonemia: Activity of urea cycle enzymes (English)

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81230-X

methylmalonyl-CoA mutase deficiency

30 March 2022

main subject

1 reference

L. J. Shapiro

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A31423

30 March 2022

M. E. Bocian

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A31423

30 March 2022

L. Raijman

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A31423

30 March 2022

S. D. Cederbaum

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A31423

30 March 2022

K. N. Shaw

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A31423

30 March 2022

language of work or name

English

0 references

publication date

1 December 1978

1 reference

full work available at URL

10 September 2017

https://api.elsevier.com/content/article/PII:S002234767881230X?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81230-X

https://api.elsevier.com/content/article/PII:S002234767881230X?httpAccept=text/plain

30 March 2022

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81230-X

The Journal of Pediatrics

30 March 2022

published in

1 reference

10 September 2017

volume

93

1 reference

10 September 2017

issue

6

1 reference

10 September 2017

page(s)

986-988

1 reference

Localisation of enzymic defect in propionicacidaemia.

10 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2878%2981230-X

Observations on the coexistence of methylmalonic acidemia and glycinemia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2878%2981230-X

Familial Protein Intolerance with Deficient Transport of Basic Amino Acids: An Analysis of 10 Patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2878%2981230-X

Hyperlysinuria with hyperammonemia. A new metabolic disorder

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2878%2981230-X

Methylmalonyl coenzyme A racemase defect: another cause of methylmalonic aciduria.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2878%2981230-X

The inhibition by methylmalonic acid of malate transport by the dicarboxylate carrier in rat liver mitochondria. A possible explantation for hypoglycemia in methylmalonic aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2878%2981230-X

Effect of methylmalonate on ketone body metabolism in developing rat brain.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2878%2981230-X

Effect of 2-Methylcitrate on Citrate Metabolism: Implications for the Management of Patients with Propionic acidemia and Methylmalonic aciduria

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2878%2981230-X

Severe hyperammonemia in a newborn infant with methylmalonyl-CoA mutase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2878%2981230-X

Lysine intolerance with periodic ammonia intoxication

7 January 2021

7

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(78)81230-X

28 October 2022

Identifiers

0 references

1 reference