Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Annals of hematology 37 (1978), S. 103-105 
    ISSN: 1432-0584
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1432-0711
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    facet.materialart.
    Unknown
    Provincetown, Mass., etc. : Periodicals Archive Online (PAO)
    Journal of Psychology. 103:2 (1979:Nov.) 227 
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Annals of hematology 37 (1978), S. 249-256 
    ISSN: 1432-0584
    Keywords: Kreatinkinase in Erythrozyten ; Genetische Anomalie ; Kreatinstoffwechsel in Erythrozyten ; Kreatinkinaseuntersuchung ; Creatine kinase in erythrocytes ; Genetic anomaly ; Creatine metabolism in erythrocytes ; Creatine kinase screening
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary In a family of Italian origin, we found four members with a considerable activity of creatine kinase inside their erythrocytes. All other clinical and hematological findings were normal. The enzyme anomaly seems to be inherited in the autosomal mode. The creatine kinase (CK) activity in freshly drawn blood was about 12 U/g Hb. The activity was higher in young red cells than in older ones. Studies with specific antibodies against human CK isoenzymes revealed the CK activity in Offprint requests to: Prof. Dr. H. Arnold (address see above) the probands' red cells to be due to about 90 % to the BB-isoenzyme normally found in brain and nerve tissue. The presence of CK in the erythrocytes does not seem to have any consequences for the energy metabolism of these cells. Creatine concentration was slightly elevated, but creatine phosphate could not be detected.
    Notes: Zusammenfassung Bei vier Angehörigen einer italienischen Familie fanden wir eine erhebliche Kreatinkinaseaktivität in den Erythrozyten. Sämtliche hämatologischen und klinischen Befunde unserer Probanden waren normal. Das abnorme Vorkommen der Kreatinkinase wird autosomal vererbt. In frisch entnommenem Blut hatte die Kreatinkinase eine Aktivität von etwa 12 U/g Hb. Die Aktivität war in jungen Erythrozyten höher als in älteren Zellen. Untersuchungen mit spezifischen Antikörpern gegen die menschlichen Kreatinkinase-(CK)Isoenzyme ergaben, daß die abnorme Kreatinkinase zu etwa 90 % dem BB-Isoenzym entspricht, das normalerweise in so hoher Konzentration nur im Gehirn- und Nervengewebe vorkommt. Die Gegenwart des Enzyms in den Erythrozyten der Probanden scheint keine Bedeutung für den Energiestoffwechsel der Zellen zu haben. Kreatin, das auch in normalen Erythrozyten vorkommt, ist auf etwa das Doppelte erhöht, während Kreatinphosphat genau wie in normalen Erythrozyten nicht nachweisbar ist.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Annals of hematology 39 (1979), S. 405-417 
    ISSN: 1432-0584
    Keywords: Glucosephosphat-Isomerase ; Enzymdefekt ; HÄmolytische AnÄmie ; Erythrozytenstoffwechsel ; Glucosephosphate isomerase ; Enzyme deficiency ; Hemolytic anemia ; Red cell metabolism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Since the first report of GPI deficiency in 1967 many patients from all over the world have been described. The patients suffer from a typical nonspherocytic hemolytic anemia with hemolytic crises during acute infections. The disease is inherited as an autosomal recessive, half of the patients are homozygotic, the others are double heterozygotes. The biochemical properties of the deficient enzymes vary widely. Thus, many well characterized enzymes have been designated as different variants. The modification of physicochemical properties surpasses kinetic aberrations. All defective variants are more or less unstable. The activity diminishes progressively, leading to a rise in G6P concentration and in red cells after aging in vitro to a dramatic impairment of glycolysis and concomittant hemolysis. The cause of the metabolic block is the diminished GPI activity itself and not an inhibition of hexokinase by the high G6P.
    Notes: Zusammenfassung Seit der Erstbeschreibung des GPI-Mangels 1967 wurden zahlreiche Patienten aus allen Teilen der Welt mitgeteilt. Die Patienten leiden an einer typischen nicht-sphÄrozytÄren hÄmolytischen AnÄmie mit krisenhafter Verschlechterung wÄhrend akuter Infektionen. Die Erkrankung wird autosomal rezessiv vererbt, die HÄlfte der Patienten ist homozygot, die anderen doppelt-heterozygot. Die biochemischen Eigenschaften der defekten Enzyme variieren stark, so da\ verschiedene Varianten beschrieben wurden. Die physiko-chemischen Eigenschaften sind hÄufiger verÄndert als die kinetischen. Alle Defekt-Varianten sind mehr oder weniger instabil. Die wÄhrend der Zellalterung fortschreitende Verminderung der GPI-AktivitÄt führt zu einem Anstieg des G6P, und bei in vitro gealterten Erythrozyten zu einem dramatischen Abfall der Glycolyserate und gleichzeitiger HÄmolyse der Zellen. Die Ursache der GlycolyseeinschrÄnkung scheint die Verminderung der GPI-AktivitÄt selbst und nicht etwa eine Hemmung der Hexokinase durch das erhöhte G6P zu sein.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Neuroradiology 16 (1978), S. 65-68 
    ISSN: 1432-1920
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Medulloblastoma and acute lymphocytic leukemia patients treated by intrathecal methotrexate and radiation were investigated by means of computerized axial tomography. More than 50% of them turned out to have acquired encephalopathy. Only gross morphologic brain defects, as visualized by computerized tomography, caused manifest clinical signs of brain dysfunction, such as epilepsy, mental retardation, paresis, and apallic syndrome. Mild morphologic changes were found even in asymptomatic children. The preferred site of defects in brain substance was the paraventricular white matter.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...