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Research 151–180 of 1000+
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Hair and Nail Relationship
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- New clinico‐genetic classification of trichothiodystrophy
- Hair loss and its management in children
- Hair Shaft Dysplasias
- Hair loss
- Diseases of Periocular Hair
- Oral retinoids-present status
- Immunological control of skin development: from homeostasis to developmental pathologies
- Madarosis
- Dermatoscopy of hair shaft disorders
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Hair and Scalp Dermatoscopy (Trichoscopy)
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- A guide to diagnosis and management of hypertrichosis
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- A rare case of woolly hair with unusual associations
- Porokeratotic Eccrine Ostial and Dermal Duct Nevus: A Report of Rare Late-Onset Solitary Lesion
- Ischemic onycholysis of the hands
- 075 Clinical investigation of JAK inhibitor Tofacitinib in scarring alopecias
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Male fertility and skin diseases
- Dupilumab in a 9-week-old with Netherton Syndrome Leads to Deep Symptom Control
- Vitamins
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients