Search
for
Sort by
Research 30 of 1000+
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Epidermolysis bullosa in animals: a review
- Dermatologia e Procedimentos Estéticos Ed. XVIII
- Dermatologia e Procedimentos Estéticos Ed. XXVII
- Líquen plano pilar e alopecia frontal fibrosante: correlação dos achados clínicos e dermatoscópicos com o grau de inflamação do exame histopatológico
- Caracterização clínica e laboratorial do acometimento dos folículos velos e da epiderme da face, pescoço e região anterossuperior do tórax na alopecia frontal fibrosante
- Avaliação do impacto da redução significativa de peso pela dieta cetogênica de muito baixa caloria nos parâmetros metabólicos, inflamatórios, hormonais e seminais de homens obesos
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Dermatopathology and molecular genetics
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Alopecia in Epidermolysis Bullosa
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Essential Oil and Important Activities of<i>Thuja orientalis</i>and<i>Thuja occidentalis</i>
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Epidermolysis Bullosa Simplex Keratinocytes Show Disturbed Mitochondrial Positioning and Activity
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Keratin disorders: from gene to therapy
- A practical guide for the study of human and murine sebaceous glands <i>in situ</i>
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Characterization of the epidermal-dermal junction in hiPSC-derived skin organoids
- Assessment of Clients' Perceptions and Satisfaction With Eyebrow Mesotherapy Treatment