Literature DB >> 572926

Clinical correlations of partial deficiency of lipoamide dehydrogenase.

R A Kark, M M Rodriguez-Budelli.   

Abstract

Reduced activities of lipoamide dehydrogenase (LAD) relative to cytochrome oxidase have been found in 12 or 26 patients with inherited ataxias. One of the 12 patients had adult-onset ataxia plus ragged-red muscle fibers. The other 11 had Friedreich syndrome or early-onset variants of this, as did 6 patients with normal enzyme activity. However, the 11 patients with reduced enzyme activity were clinically more homogeneous than the 6 with normal activity.

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Year:  1979        PMID: 572926     DOI: 10.1212/wnl.29.7.1006

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  4 in total

Review 1.  Degenerative ataxic disorders: still perplexing.

Authors:  A Harding
Journal:  Br Med J (Clin Res Ed)       Date:  1987-11-14

2.  Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy.

Authors:  J Egger; B D Lake; J Wilson
Journal:  Arch Dis Child       Date:  1981-10       Impact factor: 3.791

3.  Computed tomography in mitochondrial cytopathy.

Authors:  J Egger; B E Kendall
Journal:  Neuroradiology       Date:  1981       Impact factor: 2.804

4.  The influence of physostigmine on visual-vestibular interaction in hereditary ataxias.

Authors:  C C Tijssen; L J Endtz; C Goor
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-10       Impact factor: 10.154

  4 in total

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