Found: 16
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Establishment and Utility of SwedAD: A Nationwide Swedish Registry for Patients with Atopic Dermatitis Receiving Systemic Pharmacotherapy.
- Published in:
- Acta Dermato-Venereologica, 2023, v. 103, p. 1, doi. 10.2340/actadv.v103.7312
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- Publication type:
- Article
Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?
- Published in:
- Experimental Dermatology, 2019, v. 28, n. 10, p. 1164, doi. 10.1111/exd.13813
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- Publication type:
- Article
Quantitative image analysis of protein expression and colocalisation in skin sections.
- Published in:
- 2018
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- Publication type:
- Letter to the Editor
Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 6, p. 1070, doi. 10.1093/hmg/ddx017
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- Publication type:
- Article
Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia: Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients.
- Published in:
- Acta Dermato-Venereologica, 2016, v. 96, n. 7, p. 932, doi. 10.2340/00015555-2418
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- Publication type:
- Article
Reply to Nellen et al's Comment on the Classification of Clinical/genetic Variants of Mal de Meleda.
- Published in:
- Acta Dermato-Venereologica, 2015, v. 95, n. 8, p. 1034, doi. 10.2340/00015555-2196
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- Publication type:
- Article
Palmoplantar Keratoderma of the Gamborg-Nielsen Type is Caused by Mutations in the SLURP1 Gene and Represents a Variant of Mal de Meleda.
- Published in:
- Acta Dermato-Venereologica, 2014, v. 94, n. 6, p. 707, doi. 10.2340/00015555-1840
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- Publication type:
- Article
Generalized and Naevoid Epidermolytic Ichthyosis in Denmark: Clinical and Mutational Findings.
- Published in:
- Acta Dermato-Venereologica, 2013, v. 93, n. 3, p. 309, doi. 10.2340/00015555-1447
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- Publication type:
- Article
Keratins 2 and 4/13 in reconstituted human skin are reciprocally regulated by retinoids binding to nuclear receptor RARα.
- Published in:
- Experimental Dermatology, 2010, v. 19, n. 7, p. 674, doi. 10.1111/j.1600-0625.2010.01079.x
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- Publication type:
- Article
Genotypic and Clinical Spectrum of Self-Improving Collodion Ichthyosis: ALOX12B, ALOXE3, and TGM1 Mutations in Scandinavian Patients.
- Published in:
- Journal of Investigative Dermatology, 2010, v. 130, n. 2, p. 438, doi. 10.1038/jid.2009.346
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- Publication type:
- Article
Congenital Ichthyosis: An Overview of Current and Emerging Therapies.
- Published in:
- Acta Dermato-Venereologica, 2008, v. 88, n. 1, p. 4, doi. 10.2340/00015555-0415
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- Publication type:
- Article
Safety, Efficacy, and Dosage of 1% Pimecrolimus Cream for the Treatment of Atopic Dermatitis in Daily Practice.
- Published in:
- American Journal of Clinical Dermatology, 2006, v. 7, n. 2, p. 121, doi. 10.2165/00128071-200607020-00005
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- Publication type:
- Article
ORIGINAL ARTICLE Splice Site and Deletion Mutations in Keratin ( KRT1 and KRT10) Genes: Unusual Phenotypic Alterations in Scandinavian Patients with Epidermolytic Hyperkeratosis.
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- Journal of Investigative Dermatology, 2003, v. 121, n. 5, p. 1013, doi. 10.1046/j.1523-1747.2003.12534.x
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- Publication type:
- Article
The Clinical Spectrum of Congenital Ichthyosis in Sweden: A Review of 127 Cases.
- Published in:
- Acta Dermato-Venereologica, 2003, v. 83, p. 34, doi. 10.1080/00015555-0370
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- Publication type:
- Article
Phenotypic/Genotypic Correlations in Patients with Epidermolytic Hyperkeratosis and the Effects of Retinoid Therapy on Keratin Expression.
- Published in:
- Acta Dermato-Venereologica, 2001, v. 81, n. 3, p. 163, doi. 10.1080/000155501750376221
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- Publication type:
- Article
Keratin 4 Upregulation by Retinoic Acid In Vivo: A Sensitive Marker for Retinoid Bioactivity in Human Epidermis<sup>1</sup>.
- Published in:
- Journal of Investigative Dermatology, 2000, v. 114, n. 3, p. 487, doi. 10.1046/j.1523-1747.2000.00901.x
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- Publication type:
- Article