Found: 18
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Isotretinoin Use and Subsequent Depression and Suicide: Presenting the Evidence.
- Published in:
- American Journal of Clinical Dermatology, 2003, v. 4, n. 7, p. 493, doi. 10.2165/00128071-200304070-00005
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- Publication type:
- Article
Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.
- Published in:
- Nature Genetics, 2007, v. 39, n. 5, p. 650, doi. 10.1038/ng2020
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- Publication type:
- Article
Chronic Spontaneous Urticaria: A Questionnaire Survey.
- Published in:
- Journal of Cutaneous Medicine & Surgery, 2016, v. 20, n. 3, p. 241, doi. 10.1177/1203475415623777
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- Publication type:
- Article
Indirect Immunofluorescence for the Detection of Autoimmune Urticaria.
- Published in:
- Journal of Cutaneous Medicine & Surgery, 2016, v. 20, n. 2, p. 113, doi. 10.1177/1203475415610745
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- Publication type:
- Article
PCQoL: A Quality of Life Assessment Measure for Pachyonychia Congenita.
- Published in:
- Journal of Cutaneous Medicine & Surgery, 2015, v. 19, n. 1, p. 57, doi. 10.2310/7750.2014.14017
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- Publication type:
- Article
Compliance with Self-Examination Surveillance in Patients with Melanoma and Atypical Moles: An Anonymous Questionnaire Study.
- Published in:
- Journal of Cutaneous Medicine & Surgery, 2011, v. 15, n. 2, p. 97, doi. 10.2310/7750.2011.10011
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- Publication type:
- Article
A Large Mutational Study in Pachyonychia Congenita.
- Published in:
- Journal of Investigative Dermatology, 2011, v. 131, n. 5, p. 1018, doi. 10.1038/jid.2011.20
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- Publication type:
- Article
Heterozygous Null Alleles in Filaggrin Contribute to Clinical Dry Skin in Young Adults and the Elderly.
- Published in:
- 2009
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- Publication type:
- Letter
Filaggrin Null Alleles Are Not Associated with Psoriasis.
- Published in:
- Journal of Investigative Dermatology, 2007, v. 127, n. 8, p. 1878, doi. 10.1038/sj.jid.5700817
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- Publication type:
- Article
Null Mutations in the Filaggrin Gene (FLG) Determine Major Susceptibility to Early-Onset Atopic Dermatitis that Persists into Adulthood.
- Published in:
- Journal of Investigative Dermatology, 2007, v. 127, n. 3, p. 564, doi. 10.1038/sj.jid.5700587
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- Publication type:
- Article
Breach Delivery: Increased Solute Uptake Points to a Defective Skin Barrier in Atopic Dermatitis.
- Published in:
- Journal of Investigative Dermatology, 2007, v. 127, n. 1, p. 8, doi. 10.1038/sj.jid.5700609
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- Publication type:
- Article
Acute onset of blisters in an infant with acrodermatitis enteropathica: A case report.
- Published in:
- SAGE Open Medical Case Reports, 2021, v. 9, p. 1, doi. 10.1177/2050313X20984119
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- Publication type:
- Article
Acute onset of blisters in an infant with acrodermatitis enteropathica: A case report.
- Published in:
- SAGE Open Medical Case Reports, 2021, v. 9, p. 1, doi. 10.1177/2050313X20984119
- By:
- Publication type:
- Article
Filaggrin gene loss‐of‐function mutations constitute a factor in patients with multiple contact allergies.
- Published in:
- Contact Dermatitis (01051873), 2019, v. 80, n. 6, p. 354, doi. 10.1111/cod.13268
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- Publication type:
- Article
Trends in Invasive Cutaneous Melanoma in Saskatchewan 1970–1999.
- Published in:
- Journal of Cutaneous Medicine & Surgery, 2003, v. 7, n. 6, p. 433, doi. 10.1007/s10227-003-0159-0
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- Publication type:
- Article
Atrophying pityriasis versicolor.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Birt-Hogg-Dubé syndrome: an inherited cause of spontaneous pneumothorax.
- Published in:
- Canadian Medical Association Journal (CMAJ), 2011, v. 183, n. 9, p. E601, doi. 10.1503/cmaj.092121
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- Publication type:
- Article
Birt-Hogg-Dubé syndrome: an inherited cause of spontaneous pneumothorax.
- Published in:
- 2011
- By:
- Publication type:
- journal article