Literature DB >> 2967038

Brain glucose utilization in childhood Huntington's disease studied with positron emission tomography (PET).

A De Volder1, A Bol, C Michel, M Cogneau, P Evrard, G Lyon, A M Goffinet.   

Abstract

Brain glucose metabolism was measured in two children with early-onset Huntington's disease, using positron emission tomography with fluorodeoxyglucose (FDG) as the tracer. A marked (48%) hypometabolism was found at the level of the caudate nuclei, but other areas of the brain, particularly the cerebral cortex, were not significantly affected. Despite its different clinical presentation, Huntington's disease in children is characterized by brain metabolic alterations similar to those found in adult patients.

Entities:  

Mesh:

Substances:

Year:  1988        PMID: 2967038     DOI: 10.1016/s0387-7604(88)80046-9

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  2 in total

Review 1.  NO synthase and NO-dependent signal pathways in brain aging and neurodegenerative disorders: the role of oxidant/antioxidant balance.

Authors:  V Calabrese; T E Bates; A M Stella
Journal:  Neurochem Res       Date:  2000-10       Impact factor: 3.996

2.  Normal striatal glucose consumption in two patients with benign hereditary chorea as measured by positron emission tomography.

Authors:  T Kuwert; H W Lange; K J Langen; H Herzog; H Hefter; A Aulich; L E Feinendegen
Journal:  J Neurol       Date:  1990-04       Impact factor: 4.849

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.