These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Search MEDLINE/PubMed


  • Title: Myoadenylate deaminase deficiency in twins with recessive olivopontocerebellar atrophy.
    Author: Uziel G, Cornelio F, Gellera C, Perego C, Rimoldi M, DiDonato S.
    Journal: Ital J Neurol Sci; 1986 Feb; 7(1):107-12. PubMed ID: 3957624.
    Abstract:
    Two adult non-identical twins with autosomal recessive olivopontocerebellar degeneration (OPCA) had markedly deficient adenylate deaminase in skeletal muscle homogenates. Ischemic exercise failed to increase the blood ammonia, while lactate increased normally. Glutamate dehydrogenase and NADP-dependent malic enzyme activities in muscle mitochondria of both patients were normal. The significance of adenylate deaminase deficiency in these twins with OPCA is discussed.
    [Abstract] [Full Text] [Related] [New Search]