13 resultados para Stiekna, Konrad.

em Université de Lausanne, Switzerland


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Die heute im Archiv der katholischen Kirchengemeinde Frauenfeld, Schweiz, verwahrten ältesten Fragmente von ,Flore und Blanscheflur' gehören zu den bedeutendsten Zeugen der frühen mittelhochdeutschen Überlieferung. Der Aufsatz bietet eine detaillierte kodikologische, paläographische und dialektologische Untersuchung der in der neueren Forschung vernachlässigten Bruchstücke. Anhand einer genauen Autopsie der erhaltenen Reste können die materiale Struktur der ursprünglichen Vollhandschrift und auch der gestufte Prozess ihrer Makulierung rekonstruiert werden. Als ihr Besitzer im 14. Jahrhundert wird ein Frauenfelder Priester und Pfründstifter, Nikolaus Rüdiger von Messkirch, vermutet. Anlässlich der jeweils nicht eindeutigen Datierung und Lokalisierung der Fragmente werden grundsätzliche Überlegungen zu methodischen Problemen der mediävistischen Handschriftenkunde angestellt. Die Ergebnisse betreffen vor allem zwei Punkte: (1) Layoutmerkmale - im vorliegenden Fall: abgesetzt notierte Verse - sollten bei post quem-Datierungen nicht als Ausschlusskriterium, sondern nur als Indiz herangezogen werden; dabei sollte die Möglichkeit einer direkten Beeinflussung durch französische Vorbilder in Betracht gezogen werden, deren Layoute sich im deutschen Raum im Regelfall erst zeitlich versetzt etablieren. Exemplarisch wird ein bestimmtes Layoutmerkmal der Frauenfelder Fragmente - abgesetzte Verse mit an den rechten Rand gezogenen Reimpunkten - in seiner Belegdichte in der französischen und auch lateinischen Überlieferung seit dem 12. Jahrhundert aufgearbeitet. (2) Bei der Kriterienbildung zur Schriftsprachenbestimmung im Gefolge besonders des ,Historischen südwestdeutschen Sprachatlas' und der auf dem ,Corpus der altdeutschen Originalurkunden' beruhenden Systematisierungen ist für das 13. Jahrhundert zu wenig berücksichtigt worden, dass mit der deutschsprachigen Urkundenüberlieferung das gesamte Belegmaterial erst im letzten Viertel dieses Jahrhunderts einsetzt. Für die erste Hälfte des 13. Jahrhunderts, das die Entwicklung einer neuen literarischen Buchproduktion erlebte und das entsprechende graphematische Wandelerscheinungen erwarten lässt, bilden die daraus gewonnenen Sprachmerkmale keine zuverlässigen Abgrenzungskriterien. Sie sind im Einzelfall zu prüfen, wobei insbesondere im südwestdeutschen Raum aus Gründen des begrenzten Corpus Systematisierungen nur eingeschränkt möglich sind. Exemplarisch werden die Belege eines bestimmten Dialektmerkmals, des sog. ,,ch-Konsonantismus", anhand der gesamten Überlieferung aus dem südwestdeutschen Raum der ersten Jahrhunderthälfte erhoben. Es erweist sich, dass dieses als spezifisch bairisch (ostoberdeutsch) geltende Merkmal auch im alemannischen (westoberdeutschen) Raum für den fraglichen Zeitraum keine Ausnahme bildet. Dabei zeichnen sich Unterschiede in den Schreibungen weltlicher und geistlicher Texte ab.

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Fraud is as old as Mankind. There are an enormous number of historical documents which show the interaction between truth and untruth; therefore it is not really surprising that the prevalence of publication discrepancies is increasing. More surprising is that new cases especially in the medical field generate such a huge astonishment. In financial mathematics a statistical tool for detection of fraud is known which uses the knowledge of Newcomb and Benford regarding the distribution of natural numbers. This distribution is not equal and lower numbers are more likely to be detected compared to higher ones. In this investigation all numbers contained in the blinded abstracts of the 2009 annual meeting of the Swiss Society of Anesthesia and Resuscitation (SGAR) were recorded and analyzed regarding the distribution. A manipulated abstract was also included in the investigation. The χ(2)-test was used to determine statistical differences between expected and observed counts of numbers. There was also a faked abstract integrated in the investigation. A p<0.05 was considered significant. The distribution of the 1,800 numbers in the 77 submitted abstracts followed Benford's law. The manipulated abstract was detected by statistical means (difference in expected versus observed p<0.05). Statistics cannot prove whether the content is true or not but can give some serious hints to look into the details in such conspicuous material. These are the first results of a test for the distribution of numbers presented in medical research.

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There is a considerable discrepancy between the number of identified occupational-related bladder cancer cases and the estimated numbers particularly in emerging nations or less developed countries where suitable approaches are less or even not known. Thus, within a project of the World Health Organisation Collaborating Centres in Occupational Health, a questionnaire of the Dortmund group, applied in different studies, was translated into more than 30 languages (Afrikaans, Arabic, Bengali, Chinese, Czech, Dutch, English, Finnish, French, Georgian, German, Greek, Hindi, Hungarian, Indonesian, Italian, Japanese, Kannada, Kazakh, Kirghiz, Korean, Latvian, Malay, Persian (Farsi), Polish, Portuguese, Portuguese/Brazilian, Romanian, Russian, Serbo-Croatian, Slovak, Spanish, Spanish/Mexican, Tamil, Telugu, Thai, Turkish, Urdu, Vietnamese). The bipartite questionnaire asks for relevant medical information in the physician's part and for the occupational history since leaving school in the patient's part. Furthermore, this questionnaire is asking for intensity and frequency of certain occupational and non-occupational risk factors. The literature regarding occupations like painter, hairdresser or miner and exposures like carcinogenic aromatic amines, azo dyes, or combustion products is highlighted. The questionnaire is available on www.ifado.de/BladderCancerDoc.

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Over the last three decades, cytogenetic analysis of malignancies has become an integral part of disease evaluation and prediction of prognosis or responsiveness to therapy. In most diagnostic laboratories, conventional karyotyping, in conjunction with targeted fluorescence in situ hybridization analysis, is routinely performed to detect recurrent aberrations with prognostic implications. However, the genetic complexity of cancer cells requires a sensitive genome-wide analysis, enabling the detection of small genomic changes in a mixed cell population, as well as of regions of homozygosity. The advent of comprehensive high-resolution genomic tools, such as molecular karyotyping using comparative genomic hybridization or single-nucleotide polymorphism microarrays, has overcome many of the limitations of traditional cytogenetic techniques and has been used to study complex genomic lesions in, for example, leukemia. The clinical impact of the genomic copy-number and copy-neutral alterations identified by microarray technologies is growing rapidly and genome-wide array analysis is evolving into a diagnostic tool, to better identify high-risk patients and predict patients' outcomes from their genomic profiles. Here, we review the added clinical value of an array-based genome-wide screen in leukemia, and discuss the technical challenges and an interpretation workflow in applying arrays in the acquired cytogenetic diagnostic setting.

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BACKGROUND/AIMS: Primary hypoaldosteronism is a rare inborn disorder with life-threatening symptoms in newborns and infants due to an aldosterone synthase defect. Diagnosis is often difficult as the plasma aldosterone concentration (PAC) can remain within the normal range and thus lead to misinterpretation and delayed initiation of life-saving therapy. We aimed to test the eligibility of the PAC/plasma renin concentration (PRC) ratio as a tool for the diagnosis of primary hypoaldosteronism in newborns and infants. Meth ods: Data of 9 patients aged 15 days to 12 months at the time of diagnosis were collected. The diagnosis of primary hypoaldosteronism was based on clinical and laboratory findings over a period of 12 years in 3 different centers in Switzerland. To enable a valid comparison, the values of PAC and PRC were correlated to reference methods. RESULTS: In 6 patients, the PAC/PRC ratio could be determined and showed constantly decreased values <1 (pmol/l)/(mU/l). In 2 patients, renin was noted as plasma renin activity (PRA). PAC/PRA ratios were also clearly decreased. The diagnosis was subsequently genetically confirmed in 8 patients. CONCLUSION: A PAC/PRC ratio <1 pmol/mU and a PAC/PRA ratio <28 (pmol/l)/(ng/ml × h) are reliable tools to identify primary hypoaldosteronism in newborns and infants and help to diagnose this life-threatening disease faster. © 2015 S. Karger AG, Basel.