Literature DB >> 3467219

Glutamate and malate dehydrogenase activities in Joseph disease and olivopontocerebellar atrophy.

A Grossman, R N Rosenberg, L Warmoth.   

Abstract

The activities of brain glutamate dehydrogenase and malate dehydrogenase were not statistically different in samples from patients with autosomal dominant olivopontocerebellar atrophy or Joseph disease compared with control subject samples. These two enzymes are thus not involved in the pathogenesis of these two separate dominantly inherited diseases.

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Year:  1987        PMID: 3467219     DOI: 10.1212/wnl.37.1.106

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


  4 in total

1.  Sulfamethoxazole-trimethoprim double-blind, placebo-controlled, crossover trial in Machado-Joseph disease: sulfamethoxazole-trimethoprim increases cerebrospinal fluid level of biopterin.

Authors:  T Sakai; T Matsuishi; S Yamada; H Komori; H Iwashita
Journal:  J Neural Transm Gen Sect       Date:  1995

2.  Normal cerebellar glutamate dehydrogenase protein in spinocerebellar degeneration.

Authors:  R N Rosenberg; C Banner
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-05       Impact factor: 10.154

3.  Multiple system degeneration with glutamate dehydrogenase deficiency: pathology and biochemistry.

Authors:  S Chokroverty; W Nicklas; D C Miller; J Goldberg; J Choe; C Banner; J Thomas; R Duvoisin
Journal:  J Neurol Neurosurg Psychiatry       Date:  1990-12       Impact factor: 10.154

4.  Cerebellar glutamate metabolizing enzymes in spinocerebellar ataxia type I.

Authors:  S J Kish; L J Chang; L M Dixon; Y Robitaille; L DiStefano
Journal:  Metab Brain Dis       Date:  1994-03       Impact factor: 3.584

  4 in total

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