Lisa Biehl

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 5

Top Topics

Affordable Care Act

Quality Improvement

Randomized Controlled Trial

Top Venues

Orphanet journal of rare diseases

JMIR research protocols

This page only lists publications with an associated author ORCID identifier.

Publications

Dunja Tutus, Mandy Niemitz, Paul Lukas Plener, Joerg M Fegert, Christine Lehmann, Christa Weiss, Christine Knaevelsrud, Lisa Biehl, Miriam Rassenhofer
A web-based psychological support program for caregivers of children with rare chronic diseases: a randomized controlled trial. Orphanet journal of rare diseases 19 (1) (2024)
Dunja Tutus, Mandy Niemitz, Paul Lukas Plener, Joerg M Fegert, Christine Lehmann, Christa Weiss, Christine Knaevelsrud, Lisa Biehl, Miriam Rassenhofer
A web-based psychological support program for caregivers of children with rare chronic diseases: a randomized controlled trial. Orphanet journal of rare diseases 19 (1) (2024)
Dunja Tutus, Mandy Niemitz, Paul Lukas Plener, Joerg M Fegert, Christine Lehmann, Christa Weiss, Christine Knaevelsrud, Lisa Biehl, Miriam Rassenhofer
A web-based psychological support program for caregivers of children with rare chronic diseases: a randomized controlled trial. Orphanet journal of rare diseases 19 (1) (2024)
Svenja Litzkendorf, Tobias Hartz, Jens Göbel, Holger Storf, Frédéric Pauer, Ana Babac, Verena Lührs, Leena Bruckner-Tuderman, Franziska Schauer, Jörg Schmidtke, Lisa Biehl, Thomas Of Wagner, J-Matthias Graf von der Schulenburg, Martin Frank
Conceptualization and Implementation of the Central Information Portal on Rare Diseases: Protocol for a Qualitative Study. JMIR research protocols 7 (5) (2018)
Svenja Litzkendorf, Tobias Hartz, Jens Göbel, Holger Storf, Frédéric Pauer, Ana Babac, Verena Lührs, Leena Bruckner-Tuderman, Franziska Schauer, Jörg Schmidtke, Lisa Biehl, Thomas Of Wagner, J-Matthias Graf von der Schulenburg, Martin Frank
Metadata Correction: Conceptualization and Implementation of the Central Information Portal on Rare Diseases: Protocol for a Qualitative Study. JMIR research protocols 7 (9) (2018)