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Research 721–750 of 794
- The epidermis: rising to the surface
- Commentary: Darier-White Disease
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream
- Clinical Snippets
- [Acitretine].
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Keratosis follicularis spinulosa decalvans in a family
- Enzymology of the hair follicle.
- Ulerythema ophryogenes with multiple congenital anomalies
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Topical tacalcitol ointment can be a good therapeutic choice in erythromelanosis follicularis faciei et colli
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Topical corticosteroid in foam vehicle offers comparable coverage compared with traditional vehicles
- ELL Facilitates RNA Polymerase II–Mediated Transcription of Human Epidermal Proliferation Genes
- An audit of dermatoses at Baqai Institute of Skin Diseases, Karachi
- Trichilemmal cyst of the neck: case report and review of the literature
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- 0952 Spatial transcriptomics reveal compartmentalized dysregulation of lipid metabolism in acne vulgaris
- Dermatological aspects of primary psychiatric disorders
- Vulvovaginal involvement in Netherton syndrome: A case report
- Association between Alopecia Areata and Thyroid Dysfunction
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Common Dermatologic Disorders in Down Syndrome: Systematic Review (Preprint)
- Trichothiodystrophy in a child with occult learning disorder
- Cross‐linked features of mouse pelage hair resistant to detergent extraction
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix