Richtig erkennen und behandeln
Author:
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s15011-024-6463-2.pdf
Reference9 articles.
1. Oji V et al. Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Soreze 2009. J Am Acad Dermatol 2010; 63: 607-41
2. Renner ED et al. Comel-Netherton syndrome defined as primary immunodeficiency. J Allergy Clin Immunol 2009; 124: 536-43
3. Kathuria S et al. Sjogren-Larsson-Syndrome: importance of early diagnosis and aggressive physiotherapy. Dermatol Online J 2012; 18: 11
4. Ballin N et al. Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4. Hum Mutat 2019; 40: 2318-33
5. Oji V, Traupe H. Ichthyoses: differential diagnosis and molecular genetics. Eur J Dermatol 2006; 16: 349-59
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