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Your search keyword '"Hartz, Tobias"' showing total 45 results

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45 results on '"Hartz, Tobias"'

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1. FHIR-Datenmodell zur Übermittlung von Tumordaten zwischen Krebsregistern und IQTIG

2. Comparative evaluation of automated information extraction from pathology reports in three German cancer registries

5. Lehre 2.0 - Wie werden Social Media und Web 2.0 in die medizinische Ausbildung eingebunden? Ein systematischer Literaturüberblick [Education 2.0 - How has social media and Web 2.0 been integrated into medical education? A systematical literature review]

7. Population-Based Clinical Cancer Registration in Germany

9. Weiterentwicklung und Vernetzung der onkologischen Versorgungsstrukturen, der Qualitätssicherung und der Forschung

10. Weiterentwicklung und Vernetzung der onkologischen Versorgungsstrukturen, der Qualitätssicherung und der Forschung.

11. Development of a Maturity Model for Medical Patient Registries – A Community Approach.

13. Record Linkage - aktuelle Strategien und neue Verfahren

14. Workshop Record Linkage - aktuelle Strategien und neue Verfahren

15. Klinisches Krebsregister Niedersachsen - Datenqualität, Herausforderungen und Lösungsansätze am Beispiel der Datenlage zum Prostatakarzinom

16. Conceptualization and implementation of the central information portal on rare diseases : protocol for a qualitative study

18. Telephone health services in the field of rare diseases: A qualitative interview study examining the needs of patients, relatives, and health care professionals in Germany

19. Metadata correction : conceptualization and implementation of the central information portal on rare diseases: protocol for a qualitative study

20. Conceptualization and implementation of the central information portal on rare diseases : protocol for a qualitative study

21. Metadata Correction: Conceptualization and Implementation of the Central Information Portal on Rare Diseases: Protocol for a Qualitative Study

22. Metadata Correction: Conceptualization and Implementation of the Central Information Portal on Rare Diseases: Protocol for a Qualitative Study (Preprint)

23. Conceptualization and Implementation of the Central Information Portal on Rare Diseases: Protocol for a Qualitative Study

24. Telephone health services in the field of rare diseases: a qualitative interview study examining the needs of patients, relatives, and health care professionals in Germany

25. Chapter 14 – Orientation for Professional Users of Health Apps

26. Adopting Quality Criteria for Websites Providing Medical Information About Rare Diseases

27. Conceptualization and Implementation of the Central Information Portal on Rare Diseases: Protocol for a Qualitative Study (Preprint)

29. So selten und doch so zahlreich - Ärztliche Informationsbedarfe bei der Versorgung von Menschen mit seltenen Erkrankungen

30. Klassierungs-Wizard zur Zuordnung von Seltenen Erkrankungen auf Basis der Orphanet-Klassifikation

31. Qualitätskriterien für Informationsangebote im Internetportal ZIPSE

32. Adopting Quality Criteria for Websites Providing Medical Information About Rare Diseases

33. Education 2.0 - How has social media and Web 2.0 been integrated into medical education? A systematical literature review

34. Anforderungen an Dokumentationssysteme in der ambulanten Palliativversorgung

36. Se-atlas-cartographic representation of experts for rare diseases

37. Vision and Challenges of a Cartographic Representation of Expert Medical Centres for Rare Diseases.

39. KernPaeP – A Web-Based Pediatric Palliative Documentation System for Home Care.

41. Metadata Correction: Conceptualization and Implementation of the Central Information Portal on Rare Diseases: Protocol for a Qualitative Study.

43. [Further Development and Interoperability in Oncological Care Structures, Quality Control and Research].

44. Technical data evaluation of a palliative care web-based documentation system.

45. KernPaeP - a web-based pediatric palliative documentation system for home care.

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