(Q42257835)

English

Propionic acidaemia presenting with pancytopaenia in infancy

scientific article published on January 1980

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Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Propionic acidaemia presenting with pancytopaenia in infancy (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

1 reference

based on heuristic

inferred from title

author name string

L Sweetman

1

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

W L Nyhan

2

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

J Cravens

3

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Y Zomer

4

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

D C Plunket

5

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 January 1980

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

65-69

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

https://scigraph.springernature.com/pub.10.1007/bf01801721

0 references

Idiopathic hyperglycinemia and hyperglycinuria: a new disorder of amino acid metabolism. I

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heterozygote expression in propionyl coenzyme A carboxylase deficiency. Differences between major complementation groups

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited propionyl-CoA carboxylase deficiency in “ketotic hyperglycinemia”

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The variability of metabolite excretion in propionicacidaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Propionicacidemia, a New Inborn Error of Metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biotin-responsive propionic acidemia presenting as the rumination syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An inborn error of short-chain fatty acid metabolism. The odor-of-sweaty-feet syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biotin-responsive propionicacidaemia.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Propionicacidemia (ketotic hyperglycinemia): dietary treatment resulting in normal growth and development

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Response to dietary therapy in B 12 unresponsive methylmalonic acidemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isovaleric acidemia: Identification of isovalerate, isovalerylglycine, and 3-hydroxyisovalerate in urine of a patient previously reported as having butyric and hexanoic acidemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylmalonic/β-hydroxy-n-valeric aciduria due to methylmalonyl-Coa mutase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FURTHER OBSERVATIONS OF A PATIENT WITH HYPERGLYCINEMIA

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of propionyl-Co A carboxylase and methylcrotonyl-Co A carboxylase in a patient with methylcrotonylglycinuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal metabolites of isoleucine in a patient with propionyl-CoA carboxylase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/6796762

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01801721

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 October 2017

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