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Research 14
- Inherited Epidermolysis Bullosa: A Clinical Case
- Androgenic pattern presentation of scarring and inflammatory alopecia
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- A unique presentation of trichofolliculoma in amniotic band syndrome
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Skin Development and Disease: A Molecular Perspective
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Therapeutic potential of adult platelets and cord blood platelets in future clinical directions