Tobias Hartz

Population-Based Clinical Cancer Registration in Germany

Alexander Katalinic, Marco Halber, Martin Meyer et al. · Cancers · 2023 · 60 citations · Full text

Medicine, Oncology, Cancer Epidemiology +16

Use and importance of different information sources among patients with rare diseases and their relatives over time: a qualitative study

Svenja Litzkendorf, Martin Frank, Ana Babac et al. · BMC Public Health · 2020 · 52 citations · Full text

Social Sciences, Internal Medicine, Clinical Epidemiology +10

Expectancy, usage and acceptance by general practitioners and patients: exploratory results from a study in the German outpatient sector

Urs‐Vito Albrecht, Kambiz Afshar, Kristin Illiger et al. · Digital Health · 2017 · 37 citations · Full text

Public Affairs, Health Informatics, Health Technology Assessment +16

Information Needs of People with Rare Diseases - What Information Do Patients and their Relatives Require?

Svenja Litzkendorf, Ana Babac, Daniel Rosenfeldt et al. · Journal of Rare Disorders: Diagnosis & Therapy · 2016 · 28 citations

Veterinary Medicine, Biomedical Informatics, Disease Surveillance +12

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

Ana Babac, Martin Frank, Frédéric Pauer et al. · BMC Health Services Research · 2018 · 23 citations · Full text

Social Sciences, Health Information Management, Communication In Serious Illness +12