Publication & Citation Trends
Publications
9 total
A NOTCH3 homozygous nonsense mutation in familial Sneddon syndrome with pediatric stroke PDF
Cited by 26
OpenAlex
Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitis
Cited by 60
OpenAlex
Research Topics
Dermatology and Skin Diseases
(5)
Asthma and respiratory diseases
(4)
Food Allergy and Anaphylaxis Research
(4)
Allergic Rhinitis and Sensitization
(3)
Psoriasis: Treatment and Pathogenesis
(2)
Affiliations
Statistics Austria
Universitätsklinikum St. Pölten
National Institute of Allergy and Infectious Diseases
Karl Landsteiner University of Health Sciences
Medical University of Vienna