Search
for
Sort by
Research 511–540 of 622
- Cutaneous disorders related to obesity
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Trichoscopic findings in various alopecias at tertiary referral center: A cross-sectional study
- Reexamining the Role of Diet in Dermatology
- Intraepidermal Injections of Autologous Epidermal Cell Suspension: A new promising approach to Dermatological Disorders. Preliminary Study
- Subject Index
- [Arnozán-Dubreuilh depilating folliculitis].
- Roles of the Hedgehog Signaling Pathway in Epidermal and Hair Follicle Development, Homeostasis, and Cancer
- A systematic review of health-related quality of life outcomes in patients with advanced breast cancer treated with palbociclib
- Polypoid Cystitis and Bilateral Hydronephrosis Mimicking Urothelial Carcinoma
- Suicidality Risks Associated with Finasteride, a 5-Alpha Reductase Inhibitor: An Evaluation of Real-World Data from the FDA Adverse Event Reports
- Emerging Topical and Systemic JAK Inhibitors in Dermatology
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Wnt/β‐catenin pathway in tissue injury: roles in pathology and therapeutic opportunities for regeneration
- Hidradenitis suppurativa: A practical review of possible medical treatments based on over 350 hidradenitis patients
- Trichoscopy in genetic hair shaft abnormalities
- 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.
- New clinico‐genetic classification of trichothiodystrophy
- New insights into the role of Runx1 in epithelial stem cell biology and pathology
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Pathomechanisms of immune-mediated alopecia
- The investigation of insulin resistance and metabolic syndrome in male patients with early-onset androgenetic alopecia
- Frontal fibrosing alopecia: An update on the hypothesis of pathogenesis and treatment
- Glucocorticoids Influencing Wnt/β-Catenin Pathway; Multiple Sites, Heterogeneous Effects
- Eyebrow Loss
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Dermatologic adverse events in pediatric patients receiving targeted anticancer therapies: A pooled analysis