Monografie
Metadata correction: Conceptualization and implementation of the central information portal on rare diseases: protocol for a qualitative study
- Language
-
Englisch
- Identifier
-
1261735854
Contributor
Litzkendorf, Svenja
Hartz, Tobias
Göbel, Jens
Storf, Holger
Pauer, Frédéric
Babac, Ana
Lührs, Verena
Bruckner-Tuderman, Leena
Schauer, Franziska
Schmidtke, Jörg
Biehl, Lisa
Wagner, Thomas Otto Friedrich
Schulenburg, Johann-Matthias von der
Frank, Martin
Hartz, Tobias
Göbel, Jens
Storf, Holger
Pauer, Frédéric
Babac, Ana
Lührs, Verena
Bruckner-Tuderman, Leena
Schauer, Franziska
Schmidtke, Jörg
Biehl, Lisa
Wagner, Thomas Otto Friedrich
Schulenburg, Johann-Matthias von der
Frank, Martin
- DOI
-
10.2196/resprot.7425
- URN
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
05.08.2022, 9:31 AM CEST
Object type
- Monografie
Associated
- Litzkendorf, Svenja
- Hartz, Tobias
- Göbel, Jens
- Storf, Holger
- Pauer, Frédéric
- Babac, Ana
- Lührs, Verena
- Bruckner-Tuderman, Leena
- Schauer, Franziska
- Schmidtke, Jörg
- Biehl, Lisa
- Wagner, Thomas Otto Friedrich
- Schulenburg, Johann-Matthias von der
- Frank, Martin
Other Objects (12)
Conceptualization and implementation of the central information portal on rare diseases: protocol for a qualitative study
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Conceptualization and implementation of the central information portal on rare diseases: Protocol for a qualitative study
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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
Use and importance of different information sources among patients with rare diseases and their relatives over time: a qualitative study
Use and importance of different information sources among patients with rare diseases and their relatives over time: a qualitative study
Rare diseases on the internet: An assessment of the quality of online information
Rare diseases on the internet : an assessment of the quality of online information
Comparison of different approaches applied in Analytic Hierarchy Process - An example of information needs of patients with rare diseases
Conceptualization and implementation of the central information portal on rare diseases: protocol for a qualitative study
Metadata correction : conceptualization and implementation of the central information portal on rare diseases: protocol for a qualitative study
Conceptualization and implementation of the central information portal on rare diseases : protocol for a qualitative study
Conceptualization and implementation of the central information portal on rare diseases: Protocol for a qualitative study
Adopting quality criteria for websites providing medical information about rare diseases
Adopting Quality Criteria for Websites Providing Medical Information About Rare Diseases
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
Use and importance of different information sources among patients with rare diseases and their relatives over time: a qualitative study
Use and importance of different information sources among patients with rare diseases and their relatives over time: a qualitative study
Rare diseases on the internet: An assessment of the quality of online information
Rare diseases on the internet : an assessment of the quality of online information
Comparison of different approaches applied in Analytic Hierarchy Process - An example of information needs of patients with rare diseases
Conceptualization and implementation of the central information portal on rare diseases: protocol for a qualitative study
Metadata correction : conceptualization and implementation of the central information portal on rare diseases: protocol for a qualitative study
Conceptualization and implementation of the central information portal on rare diseases : protocol for a qualitative study
Conceptualization and implementation of the central information portal on rare diseases: Protocol for a qualitative study
Adopting quality criteria for websites providing medical information about rare diseases
Adopting Quality Criteria for Websites Providing Medical Information About Rare Diseases
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
Use and importance of different information sources among patients with rare diseases and their relatives over time: a qualitative study
Use and importance of different information sources among patients with rare diseases and their relatives over time: a qualitative study
Rare diseases on the internet: An assessment of the quality of online information
Rare diseases on the internet : an assessment of the quality of online information