8
views
0
recommends
+1 Recommend
1 collections
    0
    shares

      Call for Papers: Sex and Gender in Neurodegenerative Diseases

      Submit here before September 30, 2024

      About Neurodegenerative Diseases: 3.0 Impact Factor I 4.3 CiteScore I 0.695 Scimago Journal & Country Rank (SJR)

      • Record: found
      • Abstract: found
      • Article: found

      Biochemical Determinations in a Recently Investigated Case of McArdle’s Disease

      research-article

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Our study includes assays of the serum activities of ALD, CPK and GOT and GPT transaminase in a patient with McArdle’s disease. Muscle glycolysis has been investigated and the glycogen concentration and phosphorylase activity determined biochemically in the muscle biopsy. Our results point to three major biochemical features which are indicative of McArdle’s disease: in the blood, the failure of venous lactic acid to rise after ischaemic exercise, and in the muscle the increase of glycogen concentration and the lack of phosphorylase activity.

          Related collections

          Author and article information

          Journal
          ENE
          Eur Neurol
          10.1159/issn.0014-3022
          European Neurology
          S. Karger AG
          0014-3022
          1421-9913
          1974
          1974
          23 January 2008
          : 11
          : 1
          : 58-68
          Affiliations
          Institute of Neurology and Psychiatry (Dir.: Prof. A. Kreindler), Academy of Medical Sciences, Bucharest
          Article
          114306 Eur Neurol 1974;11:58–68
          10.1159/000114306
          4524323
          d8cb2573-4821-453d-bf54-56705e6ce782
          © 1974 S. Karger AG, Basel

          Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.

          History
          : 26 May 1973
          : 21 June 1973
          Page count
          Pages: 11
          Categories
          Paper

          Geriatric medicine,Neurology,Cardiovascular Medicine,Neurosciences,Clinical Psychology & Psychiatry,Public health
          Genetic abnormality,McArdle’s disease,Muscle phosphorylase,Ischaemic exercise,Glycogen storage

          Comments

          Comment on this article