17 results on '"Steijlen, P."'
Search Results
2. 824 Expanding the spectrum of autosomal recessive congenital ichthyosis caused by variants in NIPAL4 and PNPLA1 and evaluation of biologics interventions
3. 588 Influence of pathogenic filaggrin variants on dupilumab treatment in atopic dermatitis
4. 182 Genetic heterogeneity of STS gene mutations in a Dutch patient cohort clinically suspected for X-linked recessive ichthyosis
5. Five-Year Results of a Randomized Controlled Trial Comparing Effectiveness of Photodynamic Therapy, Topical Imiquimod, and Topical 5-Fluorouracil in Patients with Superficial Basal Cell Carcinoma
6. Three-Year Follow-Up Results of Photodynamic Therapy vs. Imiquimod vs. Fluorouracil for Treatment of Superficial Basal Cell Carcinoma: A Single-Blind, Noninferiority, Randomized Controlled Trial
7. 207 Improving diagnostic yield for filaggrin; hidden mutations in the Dutch population
8. A novel 4 bp deletion mutation in the FALDH gene segregating in a Turkish family with Sjögren-Larsson syndrome.
9. An atypical form of bullous congenital ichthyosiform erythroderma is caused by a mutation in the L12 linker region of keratin 1.
10. Melanocortin 1 receptor variants in an Irish population.
11. RET mutation screening in familial cutaneous lichen amyloidosis and in skin amyloidosis associated with multiple endocrine neoplasia.
12. Genetic linkage of the keratin type II gene cluster with ichthyosis bullosa of Siemens and with autosomal dominant ichthyosis exfoliativa.
13. Ichthyosis bullosa of Siemens is caused by mutations in the keratin 2e gene.
14. Genetic linkage between the collagen VII (COL7A1) gene and the autosomal dominant form of dystrophic epidermolysis bullosa in two Dutch kindreds.
15. Enzymatic distinction between two subgroups of autosomal recessive lamellar ichthyosis.
16. Monoclonal antibodies selected to discriminate between malignant melanomas and nevocellular nevi.
17. Immunohistologic evidence for the malignant potential of congenital melanocytic nevi.
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