(Q33637071)

28 July 2017

1 reference

title

Sudden and unexpected neonatal death: a protocol for the postmortem diagnosis of fatty acid oxidation disorders (English)

1 reference

28 July 2017

0 references

Rinaldo P

1

1 reference

28 July 2017

Yoon HR

2

1 reference

28 July 2017

Yu C

3

1 reference

28 July 2017

Raymond K

4

1 reference

28 July 2017

Tiozzo C

5

1 reference

28 July 2017

Giordano G

6

1 reference

28 July 2017

1 April 1999

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28 July 2017

Seminars in Perinatology

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28 July 2017

23

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28 July 2017

204-210

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28 July 2017

2

1 reference

Mammalian mitochondrial beta-oxidation

28 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Regulation of hepatic fatty acid oxidation and ketone body production

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Clinical and biochemical features of fatty acid oxidation disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Dissecting the spectrum of fatty acid oxidation disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Metabolic disease and sudden, unexpected death in infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Sudden neonatal death in carnitine transporter deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal death.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Comparison of post-mortem urinary and vitreous humour organic acids

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Medium chain acyl-CoA dehydrogenase deficiency in Pennsylvania: neonatal screening shows high incidence and unexpected mutation frequencies

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there correlation between genotype and phenotype?

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Medium-chain acyl-coenzyme A dehydrogenase deficiency: clinical course in 120 affected children.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

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://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Medium chain 3-ketoacyl-coenzyme A thiolase deficiency: a new disorder of mitochondrial fatty acid beta-oxidation

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

A defect in the transport of long-chain fatty acids associated with acute liver failure

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Fasting hypoketotic coma in a child with deficiency of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Cloning and characterization of the human mitochondrial 3-hydroxy-3-methylglutaryl CoA synthase gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liver.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Fatty acid oxidation disorders as primary cause of sudden and unexpected death in infants and young children: an investigation performed on cultured fibroblasts from 79 children who died aged between 0-4 years

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Inhibition of carnitine acetyltransferase by bile acids: implications for carnitine analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Retrospective biochemical screening of fatty acid oxidation disorders in postmortem livers of 418 cases of sudden death in the first year of life.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

Mitochondrial short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: a new defect of fatty acid oxidation.

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

SIDS and disorders of fatty acid oxidation: where do we go from here?

1 reference

https://api.crossref.org/works/10.1016%2FS0146-0005%2899%2980052-4

7 January 2021

10.1016/S0146-0005(99)80052-4

Identifiers

DOI

1 reference

28 July 2017

1 reference