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Research 31–60 of 1000+
- Congenital atrichia and hypotrichosis
- The eye and the skin in endocrine metabolic diseases
- Disorders of hair in children
- Acne
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- Hidradenitis Suppurativa
- The Genetics of Human Skin Disease
- 9. Immunology and Genetics
- Ichthyosis Follicularis With Alopecia and Photophobia
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Genetics of Inherited Ichthyoses and Related Diseases
- New developments in the molecular treatment of ichthyosis: review of the literature
- First Symposium of Ichthyosis Experts
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Subject Index
- Clinical Snippets
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Trichilemmal cyst of the neck: case report and review of the literature
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Hair follicles modulate skin barrier function
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- TONGUE, RED
- New clinico‐genetic classification of trichothiodystrophy
- Genetic Hair Disorders: A Review
- Connexin mutations in human disease