The Rights and Remedies of Aliens in National Courts
In: Proceedings of the annual meeting / American Society of International Law, Band 5, S. 192-210
ISSN: 2169-1118
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In: Proceedings of the annual meeting / American Society of International Law, Band 5, S. 192-210
ISSN: 2169-1118
In: Proceedings of the annual meeting / American Society of International Law, Band 5, S. 210-212
ISSN: 2169-1118
In: Political science quarterly: a nonpartisan journal devoted to the study and analysis of government, politics and international affairs ; PSQ, Band 24, Heft 3, S. 529-530
ISSN: 1538-165X
In: The annals of the American Academy of Political and Social Science, Band 20, Heft 3, S. 1-18
ISSN: 1552-3349
In: The American journal of sociology, Band 7, Heft 3, S. 424-425
ISSN: 1537-5390
In: http://hdl.handle.net/2027/nyp.33433075929863
First published in 1896. ; Bibliography: p. [3] ; Mode of access: Internet.
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In: The annals of the American Academy of Political and Social Science, Band 8, Heft 3, S. 131-140
ISSN: 1552-3349
In: Journal of the Royal United Service Institution, Band 38, Heft 199, S. 921-942
ISSN: 1744-0378
In: Political science quarterly: a nonpartisan journal devoted to the study and analysis of government, politics and international affairs ; PSQ, Band 1, Heft 3, S. 437-448
ISSN: 1538-165X
In: http://hdl.handle.net/2027/uiuc.1742639
Without music. ; Copyrighted by G.N. Harding. ; Mode of access: Internet.
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In: http://mdz-nbn-resolving.de/urn:nbn:de:bvb:12-bsb11001214-6
von Karl Köstlin ; Volltext // Exemplar mit der Signatur: München, Bayerische Staatsbibliothek -- Biogr. 506 wt
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In: http://mdz-nbn-resolving.de/urn:nbn:de:bvb:12-bsb10556760-5
Volltext // Exemplar mit der Signatur: München, Bayerische Staatsbibliothek -- J.publ.e. 218 c
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In: http://mdz-nbn-resolving.de/urn:nbn:de:bvb:12-bsb10559761-4
vom Staats-Minister von Kamptz ; Volltext // Exemplar mit der Signatur: München, Bayerische Staatsbibliothek -- J.publ.g. 373 zk
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In: http://mdz-nbn-resolving.de/urn:nbn:de:bvb:12-bsb10292063-9
von C. W. Asher ; Volltext // Exemplar mit der Signatur: München, Bayerische Staatsbibliothek -- Merc. 273-17
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In: International journal of population data science: (IJPDS), Band 4, Heft 3
ISSN: 2399-4908
Background The National Cancer Registration and Analysis Service (NCRAS), in Public Health England (PHE), collects and quality assures clinical information on all cases of cancer that occur in people living in England. The data collected supports the delivery of effective NHS cancer services.
Aim NCRAS aims to curate a clinically rich data resource, which this abstract describes.
Approach The data collected by NCRAS comes from several sources including Multi-Disciplinary Team (MDT) meetings and pathology reports. Data is reviewed by Cancer Registration Officers with the assistance of automated tools for data linkage and de-duplication of identical data sources. The data collected includes: patient identifiers; patient characteristics (e.g. sex, ethnicity); cancer specific fields (e.g. diagnosis date, cancer site, morphology, laterality, stage at diagnosis); cancer treatment fields; death information (e.g. date and cause of death); health care system information (e.g. hospital of diagnosis); and geography at diagnosis (based on patient's postcode of residence).
Results Data is submitted by 162 healthcare providers, covering over 1,700 MDTs. Population-based official statistics are available for cancers diagnosed since 1971. The data is routinely used to inform and allow evidence-based decisions about NHS service provision and patient care and to longitudinally track cancer incidence rates and survival statistics. In recent years, completeness of specific items such as stage has greatly improved. However, non-death outcomes, such as quality of life assessments and recurrence, are currently difficult to identify.
Conclusion Detailed clinical information on cancer across the patient pathway enables the measurement of the diagnosis, treatment and survival outcome of all patients diagnosed with cancer. This population-based national data resource is critical to support service provision, clinical audit, commissioning, planning of services, public health and epidemiological research; all of which contribute to improved outcomes for people diagnosed with cancer.