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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of industrial microbiology and biotechnology 17 (1996), S. 124-127 
    ISSN: 1476-5535
    Keywords: yeasts ; killer toxin ; fingerprinting ; Saccharomyces cerevisiae ; selected starters ; wine-making
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract The extreme variability of the killer phenomenon in nature, expressed differently in different strains of the same yeast species, embodies an exceptional potential for the discrimination of yeasts at the strain level. Killer-sensitive relationships between a killer reference panel of 24 yeasts belonging to 13 species of six genera, and different industrial wine-starters ofSaccharomyces cerevisiae can be used profitably for a rapid and simple fingerprinting procedure.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Antonie van Leeuwenhoek 53 (1987), S. 77-84 
    ISSN: 1572-9699
    Keywords: Saccharomyces sensu stricto ; taxonomy ; DNA reassociation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Deoxyribonucleic acid reassociation studies of 24 different wine and beer-associated strains of Saccharomyces confirmed the presence of three separate species. S. cerevisiae and S. bayanus strains had only 22% of their genomes in common. S. pastorianus, with intermediate hybridization values between S. cerevisiae and S. bayanus (52 and 72%, respectively) could possibly be a natural hybrid of the two species. S. pastorianus replaces S. carlsbergensis with which it is homologous for 93% of its genome, since the former species was described first by Hansen in 1904. These data do not agree with the results of traditional physiological tests.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Lung 101 (1948), S. 211-218 
    ISSN: 1432-1750
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Zusammenfassung Es wird über fünf zum Teil jahrelang beobachteter Fälle von atypischer Tuberkulose berichtet, ihre klinischen und röntgenologischen Symptome werden eingehend geschildert und die Differentialdiagnose unter Verwendung einschlägiger Fälle des Schrifttums erörtert. Der Fall 1 bot neben seinen Lungenerscheinungen einBoecksches Hautsarkoid, während die anderen Fälle sich nur auf die Hilusdrüsen mit Lungenbeteiligung beschränkten. Bis auf Fall 12 blieben alle gutartig. Dieser Fall 2 verdient besondere Beachtung; die anfangs als gutartig imponierende chronische Miliartbc schlug nach jahrelangem Verlauf plötzlich in eine bösartige Tbc mit letalem Ausgang um. Dieser Übergang in die hyperergische gewöhnliche Tbc läßt die innigen Beziehungen dieser zur a. Tbc erkennen. Wahrscheinlich hat sich im Fall 2 die chronische Mangelernährung der letzten Jahre auf die an sich gute Abwehr so ungünstig ausgewirkt. Allen Fällen gemeinsam war die ausgesprochen unterschwellige bis negative Tuberkulinempfindlichkeit, nur Fall 1 bot im Abheilungsstadium eine deutlich positive Hautreaktion und leitet auch damit zur typischen Tbc hinüber. Die Ausführungen haben den Zweck, die inneren vorwiegend biopathologischen Zusammenhänge zwischen typischer und atypischer Tbc, die wir als eine zu besonders hoher Immunität fähige Tbc ansehen, zu klären und die Pathogenese der sog.Schaumann-Boeckschen Krankheit näher zu beleuchten. Berücksichtigt man noch die dem Krankheitsbild besonders eigene anergische Reaktionslage, die sicherlich im Rahmen der Tuberkuloimmunität eine wesentliche Rolle spielt—für diese Anschauung sprechen auch die Ergebnisse der experimentellen Tbc-Forschung, vgl. hierzu z. B. die StudienBirghauks über Allergie, Anaphylaxie und Immunität—so wäre es mit der Benennung „atypische anergische Tbc” im Rahmen der Tbc mit seiner besonderen anatomischen und biologischen Eigenart kurz umrissen und klassifiziert.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1076
    Keywords: Type-I diabetes ; Islet cell antibodies ; Organ-specific autoimmunity ; Non-organ-specific autoimmunity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Islet cell antibodies (ICA-IgG and complement-fixing-ICA), parietal cell antibodies (PCA), intestinal epithelial cell antibodies (IECA), thyroglobulin (TgA) and thyroid microsomal antibodies (MsA), antinuclear (ANA) and reticulin antibodics (RA), were studied in 55 insulin-dependent diabetic patients (30 males and 25 females), aged 2–19 years with diabetes from a few days up to 14 years. In 58% of the diabetics one or more autoantibodies were found: ICA-IgG (31%), CF-ICA (16%), PCA (34%), TgA (9%), MsA (9%), ANA (13%), RA (2%). Autoantibodies were significantly more frequent in females (76%) than in males (43%) (P〈0.025). ICA-IgG, CF-ICA, PCA, ANA were significantly more frequent in patients than in controls. The frequency of ICA-IgG and CF-ICA was significantly higher during the first 3 years of disease than afterwards (P〈0.001); a similar pattern was observed for PCA, TgA, MsA. Of the 87 parents and 30 siblings screened for ICA-IgG, CF-ICA, PCA, IECA, TgA, MsA, ANA and RA, 42 (44%) had one or more autoantibodies, which were more frequent in females than in males. Seven relatives (6%) were ICA-IgG positive (four mothers, two fathers and one brother), and only one mother, ICA-IgG negative, was CF-ICA positive. Other autoantibodies were also more frequent in parents than in controls. Autoantibody-positive relatives have been asymptomatic up to now.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 149 (1990), S. 224-231 
    ISSN: 1432-1076
    Keywords: Diffuse connective tissue diseases ; Human leukocyte antigens (HLA) ; Antinuclear antibodies
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Diffuse connective tissue diseases (DCTD) represent an heterogeneous group of disorders characterized by systemic inflammatory reactions that are currently classified on clinical grounds. Their aetiopathogenesis is largely unknown and appears to be very complex, associating exogenous factors with an immunogenetic predisposition. In the last decade, studies on human leukocyte antigen (HLA)-disease associations and antinuclear antibodies have provided some useful clues for the diagnosis and clinical management of DCTD.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 153 (1994), S. 472-479 
    ISSN: 1432-1076
    Keywords: Antiphospholipid antibody syndrome Antiphospholipid antibodies Anticardiolipin antibodies ; Lupus anticoagulant ; Systemic lupus erythematosus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Antiphospholipid antibodies, i.e. circulating auto-antibodies to negatively charged phospholipids, are mainly observed in patients with systemic lupus erythematosus, but may also occur in individuals who lack evidence of a well-defined systemic disease. Several studies have suggested that they may play a direct role in the pathogenesis of recurrent vascular thrombosis, repeated abortions, and thrombocytopenia (socalled antiphospholipid antibody syndrome), although the mechanism by which this occurs is still poorly understood. The management of patients with antiphospholipid antibody-related thrombosis includes anti-aggregants, anticoagulants, corticosteroids, and cytotoxic drugs, but the optimum treatment is still controversial. Here we review the test systems used to detect antiphospholipid antibodies and their significance in paediatrics.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 155 (1996), S. 919-920 
    ISSN: 1432-1076
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 158 (1999), S. 281-283 
    ISSN: 1432-1076
    Keywords: Key words Takayasu arteritis ; Valvular heart disease ; Aortic regurgitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Takayasu arteritis is a rare chronic vasculitis primarily involving the aorta and its main branches. We report an adolescent girl with Takayasu arteritis who presented with an isolated aortic valve regurgitation as part of a systemic inflammatory process. This patient was initially misdiagnosed as having rheumatic heart disease and the correct diagnosis was made only 1 year later. Conclusion Takayasu arteritis should be considered among the diagnostic possibilities in patients who present with an unexplained systemic inflammatory syndrome and a cardiac murmur.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 158 (1999), S. 769-775 
    ISSN: 1432-1076
    Keywords: Key words Immune tolerance ; Auto-immunity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Fifty years ago Sir F. Macfarlane Burnet published his first fundamental contribution to the theory of immune tolerance he perfected 10 years later. Since then an impressive amount of new information on the function of the immune system has been gathered. As any original meaningful theory, Burnet's hypothesis on the development of immune tolerance has undergone extensive modifications to take into account all these new findings. An improved understanding of the mechanisms of tolerance has led to new possibilities for the treatment of auto-immune diseases. Conclusion All new information in the field of immune function is rooted in Burnet's contribution which set the stage for the development of modern immunology.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 139 (1982), S. 199-201 
    ISSN: 1432-1076
    Keywords: Pulmonary hypertrophic osteoarthropathy ; agammaglobulinemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A case of hypertrophic osteoarthropathy is described in an 8-year-old child with late-onset agammaglobulinemia, bronchiectasis and clubbing of the fingers and toes. The child presented with pain of recent onset in the legs, ankles, and knees and a diagnosis of hypertrophic osteoarthropathy was made on the basis of the radiologic findings. Therefore the differential diagnosis of bone and joint pain in agammaglobulinemic subjects must take into account hypertrophic osteoarthropathy.
    Type of Medium: Electronic Resource
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