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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
1997-1-14
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pubmed:abstractText |
Glutaryl-CoA dehydrogenase deficiency (GDD) is a recessively inherited neurometabolic disorder associated with encephalopathic crises and severe extrapyramidal symptoms. Treatment regimens including glucose and electrolyte infusions during acute illnesses, oral carnitine supplementation and/or a low-protein or lysine-restricted diet have been recommended, but their efficacy has been documented only on an anecdotal basis.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0174-304X
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pubmed:author |
pubmed-author:AthanassopoulosSS,
pubmed-author:BurlinaA BAB,
pubmed-author:ChristensenEE,
pubmed-author:DuranMM,
pubmed-author:HoffmannG FGF,
pubmed-author:LehnertWW,
pubmed-author:LeonardJ VJV,
pubmed-author:MüllerEE,
pubmed-author:MonavariA AAA,
pubmed-author:MuntauA CAC,
pubmed-author:NaughtenE RER,
pubmed-author:Plecko-StartingBB,
pubmed-author:Superti-FurgaAA,
pubmed-author:ZschockeJJ,
pubmed-author:de KlerkJ BJB
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pubmed:issnType |
Print
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pubmed:volume |
27
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
115-23
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pubmed:dateRevised |
2008-1-16
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pubmed:meshHeading |
pubmed-meshheading:8837070-Adolescent,
pubmed-meshheading:8837070-Amino Acid Metabolism, Inborn Errors,
pubmed-meshheading:8837070-Atrophy,
pubmed-meshheading:8837070-Brain,
pubmed-meshheading:8837070-Brain Diseases, Metabolic,
pubmed-meshheading:8837070-Carnitine,
pubmed-meshheading:8837070-Child,
pubmed-meshheading:8837070-Child, Preschool,
pubmed-meshheading:8837070-Combined Modality Therapy,
pubmed-meshheading:8837070-Diet, Protein-Restricted,
pubmed-meshheading:8837070-Female,
pubmed-meshheading:8837070-Follow-Up Studies,
pubmed-meshheading:8837070-Glutaryl-CoA Dehydrogenase,
pubmed-meshheading:8837070-Humans,
pubmed-meshheading:8837070-Infant,
pubmed-meshheading:8837070-Infant, Newborn,
pubmed-meshheading:8837070-Magnetic Resonance Imaging,
pubmed-meshheading:8837070-Male,
pubmed-meshheading:8837070-Neurologic Examination,
pubmed-meshheading:8837070-Oxidoreductases,
pubmed-meshheading:8837070-Oxidoreductases Acting on CH-CH Group Donors,
pubmed-meshheading:8837070-Tomography, X-Ray Computed
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pubmed:year |
1996
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pubmed:articleTitle |
Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency.
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pubmed:affiliation |
Department of Pediatrics, Univ. Marburg, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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