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Disorder of fatty acid metabolism
Known as:
Fatty Acid Metabolism Disorder
A group of genetic disorders that result from the inability to produce or use an enzyme required to oxidize fatty acids, resulting in an inability to…
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National Institutes of Health
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Related topics
Related topics
3 relations
Adrenal cortical hypofunction
Broader (2)
Disease
Lipid Metabolism Disorders
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
[Effect of carbon disulfide exposure on fatty acid metabolism in ApoE knockout and C57BL/6J mice].
Jing Liu
,
Shanlei Qiao
,
+6 authors
B. Zhu
Zhonghua lao dong wei sheng zhi ye bing za zhi…
2015
Corpus ID: 32538130
OBJECTIVE To study the influences of carbon disulfide (CS2) exposure on fatty acid metabolism in apolipoprotein E (ApoE) knockout…
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2015
2015
Case Study of a Complicated Postpartum Recovery Related to Acute Fatty Liver of Pregnancy
S. Sabella
2015
Corpus ID: 73312659
Poster Presentation Background Acute fatty liver of pregnancy (AFLP) is a fatty acid metabolism disorder that usually occurs when…
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2015
2015
[Rapid determination of 28 pesticides and tetramine in whole blood by online gel permeation chromatography coupled with gas chromatography-mass spectrometry].
B. Zhou
,
Hui-ling Li
,
Feng-tong Hao
,
Jing Ma
,
F. Dong
Zhonghua lao dong wei sheng zhi ye bing za zhi…
2015
Corpus ID: 24354472
OBJECTIVE To study the influences of carbon disulfide (CS2) exposureon fatty acid metabolism in apolipoprotein E (ApoE) knockout…
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Review
2014
Review
2014
Anesthetic agents in patients with very long‐chain acyl‐coenzyme A dehydrogenase deficiency: a literature review
C. Redshaw
,
Catherine Stewart
Paediatric anaesthesia
2014
Corpus ID: 19583098
Very long‐chain acyl‐coenzyme A dehydrongenase deficiency (VLCADD) is a rare disorder of fatty acid metabolism that renders…
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2011
2011
P-14 Multiple acyl-coa dehydrogenase deficiency: a possibly treatable condition
A. Todeschini
,
M. Cotelli
,
+6 authors
M. Filosto
Acta myologica
2011
Corpus ID: 52874419
Duchenne and Becker muscular dystrophies have similar signs and symptoms and are caused by different mutations in the same gene…
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