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Research 601–630 of 1000+
- 25-Year-Old Woman With New-Onset Seizures
- Acanthosis nigricans, insulin resistance and cutaneous virilism
- Chronic graft versus host disease and skin
- Tertiary hypothyroidism in a dog
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- SkIndia Quiz 24: Itchy papules over face
- Pharmacovigilance profiles of three generations of mineralocorticoid receptor antagonists and network toxicology analysis
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Trichoscopy in genetic hair shaft abnormalities
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- The developmental basis of fingerprint pattern formation and variation
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- New developments in the molecular treatment of ichthyosis: review of the literature
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Nail abnormalities in patients with vitiligo
- Towards the Development of AgoKirs: New Pharmacological Activators to Study Kir2.x Channel and Target Cardiac Disease
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Serum brain‐derived neurotrophic factor and vitamin D: Two concordant players controlling depression among alopecia areata and vitiligo patients: A case–control study
- Treatment of lipomas and diffuse lipomatosis with NDYAG 1064 NM laser and their impact on the quality of life
- Keratinocyte Cytokine Networks Associated with Human Melanocytic Nevus Development
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Childhood‐onset systemic lupus erythematosus with trisomy X and the increased risk for bone complications: a case report
- Drug-induced hair pigmentation: Clinical perspectives and updates