I. Hirschberg

发表

The wish to die and hastening death in amyotrophic lateral sclerosis: A scoping review

Anke Erdmann, Celia Spoden, I. Hirschberg, 2021, BMJ Supportive & Palliative Care.

International requirements for consent in biobank research: qualitative review of research guidelines

Daniel Strech, D. Strech, I. Hirschberg, 2014, Journal of Medical Genetics.

Research Guideline Recommendations for Broad Consent Forms in Biobank Research and How They Are Currently Addressed in Practice

D. Strech, I. Hirschberg, H. Kahrass, 2015, The American journal of bioethics : AJOB.

Where Public Health Meets Ethics. Conceptual Foundations and Practical Challenges of Public Health

D. Strech, J. Littmann, I. Hirschberg, 2013 .

Talking about the end of life: communication patterns in amyotrophic lateral sclerosis – a scoping review

Anke Erdmann, Celia Spoden, I. Hirschberg, 2022, Palliative care and social practice.

Evidence-based health information from the users’ perspective – a qualitative analysis

H. Bastian, D. Strech, I. Hirschberg, 2013, BMC Health Services Research.

Practice variation across consent templates for biobank research. a survey of German biobanks

D. Strech, I. Hirschberg, H. Knüppel, 2013, Front. Genet..

Current Practice of Public Involvement Activities in Biomedical Research and Innovation: A Systematic Qualitative Review

D. Strech, I. Hirschberg, J. Lander, 2014, PloS one.

Do Public Involvement Activities in Biomedical Research and Innovation Recruit Representatively? A Systematic Qualitative Review

D. Strech, I. Hirschberg, Sabine Bossert, 2016, Public Health Genomics.