Search
for
Sort by
Research 181–210 of 1000+
- Pharmacovigilance-based drug repurposing: searching for putative drugs with hypohidrosis or anhidrosis adverse events for use against hyperhidrosis
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- 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
- Analogs of human genetic skin disease in domesticated animals
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Gomez?Lopez?Hernandez syndrome: another consideration in focal congenital alopecia
- Fixed focal alopecia for 20 years
- Methods of hair loss evaluation in patients with endocrine disorders.
- Approach to Alopecia in Dogs in Clinical Practice
- A Case of Basal Cell Carcinoma Arising in Congenital Triangular Alopecia
- Line-Field Optical Coherence Tomography: Usefulness in the Non-Invasive Differential Diagnosis of Congenital Alopecia of Infancy
- Focal alopecia in the dog
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma
- Focal Asymptomatic Hair Loss in an Adolescent: A Case Report
- Aplasia cutis congenita on lumbosacral area
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Disorders of hair in children
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Alternative uses of dermoscopy in daily clinical practice: An update
- What does acne genetics teach us about disease pathogenesis?
- Hair Loss in Children
- Dermatologic manifestations of endocrine disorders
- Giant congenital cerebriform pigmented nevus of scalp: case report
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Hair Loss in Children
- Cutaneous manifestations of systemic infection in children
- Keratin disorders: from gene to therapy
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa