(Q47621398)

English

Trifunctional protein deficiency: three families with significant maternal hepatic dysfunction in pregnancy not associated with E474Q mutation.

scientific article

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scholarly article

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

Trifunctional protein deficiency: three families with significant maternal hepatic dysfunction in pregnancy not associated with E474Q mutation. (English)

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

maternal health

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Trifunctional protein deficiency

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protein deficiency

1 reference

based on heuristic

inferred from title

author name string

A Chakrapani

1

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

S Olpin

2

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

M Cleary

3

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

J H Walter

4

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

J E Wraith

5

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

G T Besley

6

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

publication date

1 December 2000

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

23

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

826-834

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

8

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

https://scigraph.springernature.com/pub.10.1023/a:1026712719416

0 references

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent acute fatty liver of pregnancy associated with a fatty-acid oxidation defect in the offspring

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assessment of the prevalence of genetic metabolic defects in acute fatty liver of pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal morbidity and mortality in 442 pregnancies with hemolysis, elevated liver enzymes, and low platelets (HELLP syndrome)

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acute fatty liver of pregnancy: a clinical study of 12 episodes in 11 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of mitochondrial trifunctional protein deficiency in a blood spot from the newborn screening card by tandem mass spectrometry and DNA analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant allele

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disorders of mitochondrial fatty acyl-CoA beta-oxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pregnancy and fetal long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved detection of long-chain fatty acid oxidation defects in intact cells using [9,10-3H]oleic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/11196108

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/A:1026712719416

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

4 February 2018

http://europepmc.org/abstract/MED/11196108

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