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Research 181–210 of 1000+
- Negative pressure wound therapy augmented full-thickness free skin grafting in the cat: outcome in 10 grafts transferred to six cats
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- CONGENITAL ATRICHIA.*
- DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control epithelial differentiation
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Budesonide for maintenance of remission in Crohn's disease
- Histologic features of alopecia areata other than peribulbar lymphocytic infiltrates
- Linear lupus panniculitis of the scalp presenting as alopecia along Blaschko’s lines: A distinct variant of lupus panniculitis in East Asians?
- Ultrastructural Localization and Quantification of Extracellular Calcium Binding Sites in Mouse Vibrissa and Human Scalp Follicles
- Remission of Alopecia Universalis Following Successful Clinical Islet Transplantation
- Surgical Facial Rejuvenation
- From basal cell carcinoma morphogenesis to the alopecia induced by hedgehog inhibitors: connecting the dots
- Alopecia
- Hypotrichosis congenita of Marie Unna
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis
- Pathological Studies of Cross‐Related Congenital Hypotrichosis in Cattle
- Global behavior of solutions in a chemotaxis model for alopecia areata with signal-dependent sensitivity
- Pityriasis Versicolor of Scalp Mimicking Alopecia Areata
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Atrichia and Papular Lesions: Report of a Case
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Hypotrichosis with juvenile macular dystrophy
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- SAT-213 Late Diagnosis of Complete Androgen Insensitivity
- PA05 A rare case of cardiocutaneous syndrome in a young child