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Research 121–150 of 1000+
- Hair Anomalies in a 6-Year-Old Girl
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Exploring Pediatric Dermatology in Skin of Color: Focus on Dermoscopy
- A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus
- Safety of skin care products during pregnancy.
- Skin and Scalp Health Benefits of a Specific Botanical Extract Blend: Results from a Double-Blind Placebo-Controlled Study in Urban Outdoor Workers
- Keratin gene mutations in disorders of human skin and its appendages
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Topical absorption and systemic toxicity
- Exploring the landscape of hair and scalp disorders in the pediatric skin of color population: A scoping review
- Atlas of Geriatric Dermatology
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Contents
- Non‐biologic immunosuppressive drugs for inflammatory and autoimmune skin diseases
- Síndrome PRIDE: una práctica forma de identificar los efectos adversos cutáneos de los inhibidores del EGFR
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin
- Birth Outcomes of Infants Born to Mothers with Alopecia Areata: A Nationwide Population-based Study in Korea
- Exploring the role of Kantavallabha rasa in Polycystic ovarian syndrome management: A pilot Study
- 865 Conditional ablation of JAK-STAT5 signaling induces anagen hair growth
- New clinico‐genetic classification of trichothiodystrophy
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome