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Research 31–60 of 59
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Current Genetics in Hair Diseases
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- A Novel Follicular Unit Excision Device for All-Purpose Hair Graft Harvesting
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Alopecia in Epidermolysis Bullosa
- Complications in Esthetic Surgery
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- The Genomic Variation in Textured Hair: Implications in Developing a Holistic Hair Care Routine
- Complications and Difficult Cases: A Neurosurgeon’s Perspective on Hair Restoration Surgery
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Dermatitis Cruris Pustulosa et Atrophicans: Scarring Alopecia Beyond Scalp Hair
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Back to the beginning: a retrospective review of the early <i>Forums</i>
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- The Nutrient–Skin Connection: Diagnosing Eating Disorders Through Dermatologic Signs
- Congenital hypotrichosis due to short anagen
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Short anagen syndrome: Case series and literature review
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Phytochemical Investigation of Tamarix aphylla (L.) Karst: A Plant of Medicinal Value from Gujarat, India
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- A Comprehensive Review on Phytochemistry and Pharmacological Effects of Stinging Nettle (Urtica dioica)
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Two females with hair loss