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Items: 15

1.

Result dissemination from clinical trials conducted at German university medical centers was delayed and incomplete.

Wieschowski S, Riedel N, Wollmann K, Kahrass H, Müller-Ohlraun S, Schürmann C, Kelley S, Kszuk U, Siegerink B, Dirnagl U, Meerpohl J, Strech D.

J Clin Epidemiol. 2019 Jun 10;115:37-45. doi: 10.1016/j.jclinepi.2019.06.002. [Epub ahead of print]

PMID:
31195110
2.

Why are so few patients rating their physicians on German physician rating websites? A qualitative study.

McLennan S, Strech D, Kahrass H.

BMC Health Serv Res. 2018 Aug 29;18(1):670. doi: 10.1186/s12913-018-3492-0.

3.

Current practices for access, compensation, and prioritization in biobanks. Results from an interview study.

Langhof H, Kahrass H, Illig T, Jahns R, Strech D.

Eur J Hum Genet. 2018 Nov;26(11):1572-1581. doi: 10.1038/s41431-018-0228-x. Epub 2018 Aug 8.

PMID:
30089824
4.

The Public's Awareness of and Attitude Toward Research Biobanks - A Regional German Survey.

Bossert S, Kahrass H, Strech D.

Front Genet. 2018 May 24;9:190. doi: 10.3389/fgene.2018.00190. eCollection 2018.

5.

The spectrum of ethical issues in a Learning Health Care System: a systematic qualitative review.

McLennan S, Kahrass H, Wieschowski S, Strech D, Langhof H.

Int J Qual Health Care. 2018 Apr 1;30(3):161-168. doi: 10.1093/intqhc/mzy005. Review.

PMID:
29394354
6.

Participatory improvement of a template for informed consent documents in biobank research - study results and methodological reflections.

Bossert S, Kahrass H, Heinemeyer U, Prokein J, Strech D.

BMC Med Ethics. 2017 Dec 20;18(1):78. doi: 10.1186/s12910-017-0232-7.

7.
8.

Public Awareness and Use of German Physician Ratings Websites: Cross-Sectional Survey of Four North German Cities.

McLennan S, Strech D, Meyer A, Kahrass H.

J Med Internet Res. 2017 Nov 9;19(11):e387. doi: 10.2196/jmir.7581.

9.

Ethical issues in obesity prevention for school children: a systematic qualitative review.

Kahrass H, Strech D, Mertz M.

Int J Public Health. 2017 Dec;62(9):981-988. doi: 10.1007/s00038-017-1027-9. Epub 2017 Aug 11. Review.

PMID:
28801690
10.

Access policies in biobank research: what criteria do they include and how publicly available are they? A cross-sectional study.

Langhof H, Kahrass H, Sievers S, Strech D.

Eur J Hum Genet. 2017 Feb;25(3):293-300. doi: 10.1038/ejhg.2016.172. Epub 2016 Dec 21.

11.

Current state of ethics literature synthesis: a systematic review of reviews.

Mertz M, Kahrass H, Strech D.

BMC Med. 2016 Oct 3;14(1):152. Review.

12.

The Full Spectrum of Clinical Ethical Issues in Kidney Failure. Findings of a Systematic Qualitative Review.

Kahrass H, Strech D, Mertz M.

PLoS One. 2016 Mar 3;11(3):e0149357. doi: 10.1371/journal.pone.0149357. eCollection 2016.

13.

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

Strech D, Kahrass H, Hirschberg I.

Am J Bioeth. 2015;15(9):60-3. doi: 10.1080/15265161.2015.1062169. No abstract available.

PMID:
26305759
14.

The full spectrum of ethical issues in the care of patients with ALS: a systematic qualitative review.

Seitzer F, Kahrass H, Neitzke G, Strech D.

J Neurol. 2016 Feb;263(2):201-209. doi: 10.1007/s00415-015-7867-4. Epub 2015 Jul 30. Review.

PMID:
26223806
15.

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

Hirschberg I, Kahrass H, Strech D.

J Med Genet. 2014 Dec;51(12):773-81. doi: 10.1136/jmedgenet-2014-102692. Epub 2014 Oct 28.

PMID:
25351952

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