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Abstract

Thomas Cranmer's register in Lambeth Palace Library is little known and not yet published. This article surveys and summarizes the author's researches over twenty-five years in preparing an edition of that document. The register is not as complete as many medieval Canterbury registers. Nonetheless, it shows how the royal supremacy developed in a church cut off from Roman jurisdiction. There are many parallels with medieval patterns of ecclesiastical jurisdiction, and Cranmer seems to have been unable or unwilling to make large-scale changes in prevailing practice. Nonetheless, during the reign of Edward VI, the register illustrates a reforming archbishop at work, as he tried to implement evangelical reforms in diocese and province. The untimely death of Edward VI cut short these reforming measures, and the accession of Mary led to Cranmer's deprivation, when the formal record of his register ends.  相似文献   

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Review Article     
Hintikka  Jaakko  Bohan-Broderick  Paul 《Synthese》2000,124(3):433-445
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Review Article     
The Pope's Armada Gordon Urquhart, 1995 London: Bantam 441 pp., £16.99 hb ISBN 0–593–033884  相似文献   

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As monarch of the lordship and (since 1541) kingdom of Ireland, King Henry VIII and his successors imposed the same ecclesiastical and religious policies they devised for England on Dublin, the most English city in Tudor Ireland. Far-reaching changes were effected to quite a remarkable degree. Yet the English Reformation failed to take root in the Irish city. This paper explores both the course of the Reformation in the capital of English Ireland and the reasons for its general failure. It also highlights some implications of Dublin’s experience relevant to continuing debates in English Reformation studies.  相似文献   

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Chiari type I malformation has traditionally been defined as a downward herniation of the cerebellar tonsils of 5 mm through the foramen magnum and it is likely associated with a volumetrically reduced posterior fossa. Syringomyelia is commonly associated with Chiari type I malformation. We estimate the prevalence of these two conditions and determine that they are more common than previously expected. We identify the genetic syndromes associated with some cases of Chiari type I malformation, and we provide evidence in favor of a genetic hypothesis for at least a subset of the nonsyndromic cases.  相似文献   

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