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      Tubular Reabsorption of Bicarbonate in Transplanted Cadaver Kidneys

      Nephron

      S. Karger AG

      Bicarbonate reabsorption, Renal tubular acidosis, Urinary pCO2 , Cadaver kidney transplantation

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          Abstract

          The urinary bicarbonate excretion following administration of sodium bicarbonate was examined in 25 necrokidney-transplanted patients 14–60 days after the operation, and in 10 patients with mild, chronic renal diseases. The loss of bicarbonate in the urine was not greater in the transplanted patients than in the controls when the degree of alkalosis and the glomerular filtration were taken into consideration. Neither was there any difference between the ability of the kidneys to increase the urine pCO<sub>2</sub> by alkalosis.

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          Author and article information

          Journal
          NEF
          Nephron
          10.1159/issn.1660-8151
          Nephron
          S. Karger AG
          1660-8151
          2235-3186
          1973
          1973
          27 November 2008
          : 10
          : 4
          : 216-221
          Affiliations
          Medical Department P, Rigshospitalet, Copenhagen
          Article
          180190 Nephron 1973;10:216–221
          10.1159/000180190
          4573697
          © 1973 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.

          Page count
          Pages: 6
          Categories
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