Deficiencies within the Pyruvate Dehydrogenase Complex: Clinical and Pathological Correlates
Author:
Publisher
Wiley
Subject
Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1985.tb03779.x/fullpdf
Reference20 articles.
1. A defect in pyruvate decarboxylase in a child with an intermittent movement disorder;Blass;Journal of Clinical Investigation,1970
2. Clinical studies of a patient with pyruvate decarboxylase deficiency;Blass;Archives of Neurology,1971
3. Low activities of the pyruvate andoxyglutarate dehydrogenase complexes in five patients with Friedreich's ataxia;Blass;New England Journal of Medicine.,1976
4. Pyruvate dehydrogenase deficiency in spinocerebellar degenerations;Kark;Neurology,1979
5. Pyruvate decarboxylase deficiency in a patient with subacute necrotising encephalomyelopathy;Farmer;Neurology,1973
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Neuroradiologia della sindrome di Alpers;Rivista di Neuroradiologia;1992-04
2. Estimation of pyruvate dehydrogenase (E1) activity in human skeletal muscle; three cases with E1 deficiency;Clinica Chimica Acta;1988-01
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