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Research 601–630 of 791
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Topical tacalcitol ointment can be a good therapeutic choice in erythromelanosis follicularis faciei et colli
- Hair and Scalp Disorders in a Tuscan Pediatric Dermatological Outpatient Clinic: A Clinical and Epidemiological Evaluation
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Regulation of Epidermal Ferritin Expression Influences Systemic Iron Homeostasis
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Madarosis from mitochondriopathy
- ELL Facilitates RNA Polymerase II–Mediated Transcription of Human Epidermal Proliferation Genes
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- Connexin mutations in human disease
- An audit of dermatoses at Baqai Institute of Skin Diseases, Karachi
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- “Peeling paint” dermatosis in a leukemia patient
- A case of acquired trichorrhexis nodosa after applying new hair spray
- Trichilemmal cyst of the neck: case report and review of the literature
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Ectodermal Dysplasia: Variable Expressions
- Dermatological aspects of primary psychiatric disorders
- Vulvovaginal involvement in Netherton syndrome: A case report
- Association between Alopecia Areata and Thyroid Dysfunction
- “Degeneration” in Dermatopathology
- Madarosis and facial keratinaceous spines
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Comparative study of cutaneous manifestations in patients with chronic kidney disease , patients on haemodialysis, and renal transplant recipients
- Trichothiodystrophy in a child with occult learning disorder
- ETHANOLAMINE