Found: 17
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Notch-ing up knowledge on molecular mechanisms of skin fibrosis: focus on the multifaceted Notch signalling pathway.
- Published in:
- Journal of Biomedical Science, 2021, v. 28, n. 1, p. 1, doi. 10.1186/s12929-021-00732-8
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- Publication type:
- Article
First Case of KRT2 Epidermolytic Nevus and Novel Clinical and Genetic Findings in 26 Italian Patients with Keratinopathic Ichthyoses.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 20, p. 7707, doi. 10.3390/ijms21207707
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- Publication type:
- Article
Multiple Skin Squamous Cell Carcinomas in Junctional Epidermolysis Bullosa Due to Altered Laminin-332 Function.
- Published in:
- International Journal of Molecular Sciences, 2020, v. 21, n. 4, p. 1426, doi. 10.3390/ijms21041426
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- Publication type:
- Article
Epidermolysis Bullosa-Associated Squamous Cell Carcinoma: From Pathogenesis to Therapeutic Perspectives.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 22, p. 5707, doi. 10.3390/ijms20225707
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- Publication type:
- Article
Case report: bullous pemphigoid development underlies dystrophic epidermolysis bullosa disease worsening.
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- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.929286
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- Publication type:
- Article
Cross-Sectional Study on Autosomal Recessive Congenital Ichthyoses: Association of Genotype with Disease Severity, Phenotypic, and Ultrastructural Features in 74 Italian Patients.
- Published in:
- Dermatology (10188665), 2024, v. 240, n. 3, p. 397, doi. 10.1159/000536366
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- Publication type:
- Article
IgE Sensitization Profile in Patients with Netherton Syndrome.
- Published in:
- International Archives of Allergy & Immunology, 2022, v. 183, n. 12, p. 1291, doi. 10.1159/000526409
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- Publication type:
- Article
RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell-cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development.
- Published in:
- 2022
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- Publication type:
- journal article
Hoarse cry in a newborn with epidermolysis bullosa simplex, generalized severe.
- Published in:
- Pediatric Dermatology, 2020, v. 37, n. 2, p. 393, doi. 10.1111/pde.14105
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- Publication type:
- Article
Phenotypic Features of Epidermolysis Bullosa Simplex due to KLHL24 Mutations in 3 Italian Cases.
- Published in:
- 2019
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- Publication type:
- Case Study
A Postzygotic ATP2A2 Novel Mutation Identified by Next-generation Sequencing in Mosaic Darier Disease.
- Published in:
- 2019
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- Publication type:
- Case Study
Epidermolysis Bullosa (EB) Acquisita in an Adult Patient with Previously Unrecognized Mild Dystrophic EB and Biallelic COL7A1 Mutations.
- Published in:
- Acta Dermato-Venereologica, 2018, v. 98, n. 4, p. 411, doi. 10.2340/00015555-2851
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- Publication type:
- Article
Proteasome-mediated degradation of keratins 7, 8, 17 and 18 by mutant KLHL24 in a foetal keratinocyte model: Novel insight in congenital skin defects and fragility of epidermolysis bullosa simplex with cardiomyopathy.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 8, p. 1308, doi. 10.1093/hmg/ddab318
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- Publication type:
- Article
Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study.
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- Biomedicines, 2022, v. 10, n. 6, p. 1460, doi. 10.3390/biomedicines10061460
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- Publication type:
- Article
A Novel Phenotype of Junctional Epidermolysis Bullosa with Transient Skin Fragility and Predominant Ocular Involvement Responsive to Human Amniotic Membrane Eyedrops.
- Published in:
- Genes, 2021, v. 12, n. 5, p. 716, doi. 10.3390/genes12050716
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- Publication type:
- Article
Two Italian Patients with ELOVL4 -Related Neuro-Ichthyosis: Expanding the Genotypic and Phenotypic Spectrum and Ultrastructural Characterization.
- Published in:
- Genes, 2021, v. 12, n. 3, p. 343, doi. 10.3390/genes12030343
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- Publication type:
- Article
Combination Treatment with Hydroxytyrosol and Vitamin E Improves NAFLD-Related Fibrosis.
- Published in:
- Nutrients, 2022, v. 14, n. 18, p. N.PAG, doi. 10.3390/nu14183791
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- Publication type:
- Article