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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 69 (1980), S. 369-374 
    ISSN: 0027-5107
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 62 (1982), S. 327-332 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary BrdU-incorporation techniques were used to study the cell cycle in 18 cases of Fanconi's anemia (FA). By comparison with controls, a significant slowing of the cell cycle of lymphocytes in vitro was observed in all FA patients, and possibly in FA heterozygotes, although to a lesser degree. It is probable that the demonstration of the slowing is dependent on the culture conditions. No slowing was observed in other patients affected by at least one of the symptoms of FA. The slow cell cycle of FA cells is mostly due to a very long G2-phase. A relationship between slow cell cycle and chromatid anomalies exists, the slower cells being significantly more frequently carriers of radial figures than the faster cells, in the same patient.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1439-0973
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Fifteen patients aged between three and 27 years were examined clinically and immunologically. Common to all patients were severe recurring cutaneous and pulmonary staphylococcal infections, chronic eczema, eosinophilia and an extremely elevated serum IgE level. Eight of the patients had in addition facial dysplasia characterised by coarse features, prognathism and poorly formed external ears. Marked osteoporosis, particularly of the vertebral bodies, was observed in eight patients. A constant defect of granulocyte chemotaxis was found in only three patients; fluctuating or constantly normal chemotaxis occurred in six patients. Polyclonal hypergammaglobulinemia was detected in 14 patients, elevated IgD in two patients, a partial T-cell defect in two patients and a history of lack of antibody response in one patient. Therapeutic trials with immunoglobulins, transfer factor, levamisole and anti-H2 receptor-antihistamines did not produce lasting or satisfactory clinical or immunological results in the pathogenetically unidentified disease.
    Notes: Zusammenfassung Fünfzehn Patienten im Alter von drei bis 27 Jahren wurden klinisch und infektionsimmunologisch untersucht. Allen gemeinsam waren schwere rezidivierende, kutane und pulmonale Staphylokokken-infektionen, ein chronisches Ekzem, Bluteosinophilie und eine extreme Erhöhung des Serum-IgE-Spiegels. Acht der Patienten wiesen zudem eine faziale Dysmorphie auf, die durch grobe Gesichtszüge, Prognathie und schlecht modellierte Ohrmuscheln charakterisiert ist. Eine deutliche Osteoporose, vor allem der Wirbelkörper, wurde bei acht Patienten beobachtet. Ein konstanter Granulozyten-Chemotaxis-Defekt fand sich nur in drei Fällen, variable oder konstant normale Chemotaxis-Befunde traten in sechs Fällen auf. Eine polyklonale Hypergammaglobulinämie (14 Patienten), erhöhtes IgD (zehn Patienten) wurden nachgewiesen, ebenso ein partieller T-Zell-Defekt (zwei Patienten) und eine fehlende anamnestische Antikörperantwort bei einem Patienten. Therapieversuche mit Immunglobulinen, Transfer-Faktor, Levamisol und anti-H2-Rezeptor-Antihistaminika blieben bei der pathogenetisch ungeklärten Erkrankung ohne anhaltende oder befriedigende klinische und immunologische Ergebnisse.
    Type of Medium: Electronic Resource
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