Search
for
Sort by
Research 931–960 of 1000+
- Methotrexate in dermatology
- Central hair loss in African American women: Incidence and potential risk factors
- ROOT HAIR DEFECTIVE SIX‐LIKE4 (RSL4) promotes root hair elongation by transcriptionally regulating the expression of genes required for cell growth
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- MENSTRUAL DISORDERS IN ADOLESCENTS
- Aging of the hair follicle pigmentation system
- Vitiligo and alopecia areata: apples and oranges?
- Alopecia areata − animal models
- 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.
- Causes of hair loss and the developments in hair rejuvenation
- Frontal fibrosing alopecia: reflections and hypotheses on aetiology and pathogenesis
- Management of congenital ichthyoses: European guidelines of care, part two
- Apoptosis May Explain the Pharmacological Mode of Action and Adverse Effects of Isotretinoin, Including Teratogenicity
- Dermoscopy for the Pediatric Dermatologist Part I: Dermoscopy of Pediatric Infectious and Inflammatory Skin Lesions and Hair Disorders
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Hair Follicle: A Novel Source of Multipotent Stem Cells for Tissue Engineering and Regenerative Medicine
- Perspectives of Kennedy's disease
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- The population dynamics of cancer: a Darwinian perspective
- Polycystic Ovaries Are Inherited as an Autosomal Dominant Trait: Analysis of 29 Polycystic Ovary Syndrome and 10 Control Families
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Frontal Fibrosing Alopecia: An Update on Pathogenesis, Diagnosis, and Treatment
- Acne keloidalis nuchae: prevalence, impact, and management challenges
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- Lineage Analysis of Epidermal Stem Cells
- Alopecia areata: What’s new in epidemiology, pathogenesis, diagnosis, and therapeutic options?
- Skin grafting for the treatment of chronic leg ulcers – a systematic review in evidence‐based medicine
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Skin Keratins