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Research 361–390 of 484
- The ultrastructure of the interfollicular epidermis of the hairless (hr/hr) mouse
- Ichthyosis hystrix
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Disorders of Keratinization
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Phase II Evaluation of VDC‐1101 in Canine Cutaneous T‐Cell Lymphoma
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- New developments in the molecular treatment of ichthyosis: review of the literature
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Hodgkin′s lymphoma presenting as alopecia
- AN UPDATE OF HAIR SHAFT DISORDERS
- Kaposi varicelliform eruption
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Follicular unit extraction [FUE] – One procedure, many uses
- Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream
- MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE
- Positive Impact of Fish Oil on Diabetic and Hypercholestrolemic Skin Disorders
- Mycosis Fungoides in Elderly Adults—A Diagnostic Challenge
- Momentary fluke of cyclosporine in incidental repigmentation and hypertrichosis of hair
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- “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
- The skin as a window on internal disorders: Two cases of internal malignancy and hypervitaminosis B12
- Skin-infiltrating CD4+ lymphoma cells depend on hair follicle-derived IL-7
- Trichorrhexis Invaginata and Netherton’s Syndrome