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Research 661–690 of 1000+
- Trichonodosis: a case report and literature review
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Congenital milia En plaque on scalp
- Epidermis-specific ablation of claudin-1 in adult mice demonstrates the essential role of a tight junction barrier in skin homeostasis
- Mesenchymal Stem Cells for the Treatment of Skin Diseases
- A Congenital Hair Defect: Trichoschisis With Alternating Birefringence and Low Sulfur Content
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Giant congenital cerebriform pigmented nevus of scalp: case report
- Hormonal Therapy for Acne
- Congenital Triangular Alopecia: A Case of Effective Response with 5% Topical Minoxidil in a Male Adolescent
- LB1672 Senescent melanocytes in nevus skin stimulate hair growth
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Lateral plate mesoderm directs human amnion and ventral skin organoid formation
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- MENSTRUAL DISORDERS IN ADOLESCENTS
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Acanthosis nigricans, insulin resistance and cutaneous virilism
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- The Hirsute Woman: Challenges in Evaluation and Management
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- Tanshinone IIA pretreatment protects free flaps against hypoxic injury by upregulating stem cell-related biomarkers in epithelial skin cells
- Symmetrical alopecia in the dog
- Dupilumab in a 9-week-old with Netherton Syndrome Leads to Deep Symptom Control
- Congenital triangular alopecia - A case report