Leucocyte Glutamate Dehydrogenase in Various Hereditary Ataxias

Author:

Barbeau A.,Charbonneau M.,Cloutier T.

Abstract

SUMMARY:Leucocyte Glutamate Dehydrogenase (GDH) activity was measured in 44 patients with various forms of ataxia and 44 age and sex-matched normal controls. The only significant change found was a moderate decrease in activity in Freidreich's ataxia and a few patients with OPCA. This decreased activity is not primary to the disease but probably reflects a regulatory defect affecting mitochondrial membranes in these patients.

Publisher

Cambridge University Press (CUP)

Subject

Clinical Neurology,Neurology,General Medicine

Cited by 13 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. Leukocyte glutamate dehydrogenase and CSF amino acids in late onset ataxias;Acta Neurologica Scandinavica;2009-01-29

2. Leukocyte glutamate dehydrogenase and CSF amino acids in late onset ataxias;Acta Neurologica Scandinavica;2009-01-29

3. Die olivopontozerebelläre Atrophie - ein heterogenes morphologisches Syndrom;Fortschritte der Neurologie · Psychiatrie;1997-12

4. Frataxin is Reduced in Friedreich Ataxia Patients and is Associated with Mitochondrial Membranes;Human Molecular Genetics;1997-10-01

5. Glutamate Dehydrogenase Deficiency in Machado-Joseph Disease;Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques;1993-05

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