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Research 421–450 of 500
- 152 Alopecia patterns in patients with autosomal receesive congenital ichthyosis
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Characterization of an autoimmune condition associated with AEC syndrome
- Trichothiodystrophy in a child with occult learning disorder
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- CD8+ mycosis fungoides clinically masquerading as alopecia areata
- Genetics of Inherited Ichthyoses and Related Diseases
- Ichthyosis hystrix
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Chronic graft versus host disease and skin
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Phase II Evaluation of VDC‐1101 in Canine Cutaneous T‐Cell Lymphoma
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Hodgkin′s lymphoma presenting as alopecia
- AN UPDATE OF HAIR SHAFT DISORDERS
- Alopecia areata after mogamulizumab treatment
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Follicular unit extraction [FUE] – One procedure, many uses
- Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream
- Prolonged Drug-Induced Hypersensitivity Syndrome/DRESS With Alopecia Areata and Autoimmune Thyroiditis
- Alopecia areata-like presentations with mogamulizumab therapy
- “Degeneration” in Dermatopathology
- Co-Expression Pattern of Artemis Serine 516 Phosphorylation with Indicators Involving in Differentiation, Proliferation and Apoptosis of Human Anagen Hair Follicles: An Immunofluorescence Double-Staining Study
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Skin-infiltrating CD4+ lymphoma cells depend on hair follicle-derived IL-7
- Trichorrhexis Invaginata and Netherton’s Syndrome
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Multisystem Inflammatory Syndrome in Adults (MIS-A) and SARS-CoV2: An Evolving Relationship
- Alopecia Mucinosa: Report of a Case and Review