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Related Experiment Video

Updated: May 22, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease

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Published on: June 16, 2020

[The German network for systemic sclerosis (DNSS): current data on diagnostics and therapy].

N Hunzelmann¹, T Krieg,

¹Klinik und Poliklinik für Dermatologie und Venerologie, Klinikum der Universität zu Köln, 50937, Köln, Deutschland. Nico.Hunzelmann@uni-koeln.de

Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete

|May 1, 2012

Summary

National cooperation among specialized centers is crucial for rare disease research. The German network for systemic sclerosis (DNSS) patient register, with over 3,100 patients, supports clinical and basic research, fostering international collaboration.

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Area of Science:

Rheumatology and rare disease research.
Clinical and translational science.

Context:

Progress in rare disease understanding requires national collaboration.
The German network for systemic sclerosis (DNSS) unites specialized centers.
Systemic sclerosis (SSc) is a rare autoimmune disease requiring specialized care.

Purpose:

To present the results and significance of the German network for systemic sclerosis (DNSS) patient register.
To highlight the role of national cooperation in rare disease research.
To showcase the DNSS register as a foundation for clinical and basic studies.

Summary:

The DNSS patient register includes over 3,100 systemic sclerosis (SSc) patients.
It collects prospective data on diagnostics and therapy.
The register is a key resource for national and international research efforts.

Impact:

The DNSS register serves as a successful basis for clinical research and basic studies.
It facilitates international cooperation in SSc research.
The data supports advancements in understanding SSc pathophysiology and treatment.