Anja Diem

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 7

Top Topics

Intellectual Disability

Psychometric Properties

End Stage Renal Disease

Patient Reported Outcomes

Top Venues

Orphanet journal of rare diseases

The British journal of dermatology

Diagnostics (Basel, Switzerland)

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

Publications

Gudrun Salamon, Sophie Strobl, Ursula Field-Werners, Anja Diem, Agnes Schwieger-Briel, Elena Pope
Psychometric Properties of the Instrument for Scoring Clinical Outcomes of Research for Epidermolysis Bullosa patient score (iscorEB-p): a patient-reported outcome measure. The British journal of dermatology 191 (1) (2024)
Gudrun Salamon, Sophie Strobl, Ursula Field-Werners, Anja Diem, Agnes Schwieger-Briel, Elena Pope
Psychometric Properties of the Instrument for Scoring Clinical Outcomes of Research for Epidermolysis Bullosa patient score (iscorEB-p): a patient-reported outcome measure. The British journal of dermatology 191 (1) (2024)
Gudrun Salamon, Ursula Field-Werners, Sophie Strobl, Vinzenz Hübl, Anja Diem
Facing the complex challenges of people with epidermolysis bullosa in Austria: a mixed methods study on burdens and helpful practices. Orphanet journal of rare diseases 19 (1) (2024)
Gudrun Salamon, Ursula Field-Werners, Sophie Strobl, Vinzenz Hübl, Anja Diem
Facing the complex challenges of people with epidermolysis bullosa in Austria: a mixed methods study on burdens and helpful practices. Orphanet journal of rare diseases 19 (1) (2024)
Gudrun Salamon, Sophie Strobl, Ursula Field-Werners, Anja Diem, Agnes Schwieger-Briel, Elena Pope
Psychometric Properties of the Instrument for Scoring Clinical Outcomes of Research for Epidermolysis Bullosa patient score (iscorEB-p): a patient-reported outcome measure. The British journal of dermatology 191 (1) (2024)
Gudrun Salamon, Ursula Field-Werners, Sophie Strobl, Vinzenz Hübl, Anja Diem
Facing the complex challenges of people with epidermolysis bullosa in Austria: a mixed methods study on burdens and helpful practices. Orphanet journal of rare diseases 19 (1) (2024)
Alfred Klausegger, Niklas Jeschko, Markus Grammer, Jan Cemper-Kiesslich, Franz Neuhuber, Anja Diem, Hannelore Breitenbach-Koller, Gabriele Sander, Dieter Kotzot, Johann Wolfgang Bauer, Martin Laimer
Recessive Dystrophic Epidermolysis bullosa due to Hemizygous 40 kb Deletion of COL7A1 and the Proximate PFKFB4 Gene Focusing on the Mutation c.425A>G Mimicking Homozygous Status. Diagnostics (Basel, Switzerland) 12 (10) (2022)