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Research 481–510 of 1000+
- Current Genetics in Hair Diseases
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Hair restoration surgery: pre-surgical considerations and pitfalls
- Graham-Little Piccardi Lassueur Syndrome and review of the literature
- Frontal fibrosing alopecia
- Clinical effectiveness of finasteride versus hydroxychloroquine in the treatment of frontal fibrosing alopecia: A randomized controlled trial
- The Skin Microbiome: Current Landscape and Future Opportunities
- Animal and in vitro Models for the Study of Hair Follicles
- Granuloma annulare associated with Hodgkin's disease
- Two Clinically Unusual Cases of Folliculotropic Mycosis Fungoides: One with and the Other without Syringotropism
- Advances in Laser Therapy for Hidradenitis Suppurativa: A Systematic Assessment of Current Evidence
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Premature Senescence of Balding Dermal Papilla Cells In Vitro Is Associated with p16INK4a Expression
- Swiss Practice Recommendations for the Management of Hidradenitis Suppurativa/Acne Inversa
- Lichen planopilaris and frontal fibrosing alopecia: review and update of diagnostic and therapeutic features
- Frontal Fibrosing Alopecia Coexisting with Lupus Erythematosus: Poor Response to Hydroxychloroquine
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Two Cases of Hidradenitis Suppurativa Treated with Adalimumab at the Department of Dermatology and Venereology, Clinical Hospital Mostar.
- Culture Strategy Determines the Differentiation Status of Sweat Gland Cells
- An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution
- A review of isotretinoin in the treatment of frontal fibrosing alopecia
- Two Cases of Hidradenitis Suppurativa Treated with Adalimumab at the Department of Dermatology and Venereology, Clinical Hospital Mostar.
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Visualising Androgen Receptor Activity in Male and Female Mice
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation.
- Dermoscopy of skin infestations and infections (entomodermoscopy) – Part I: dermatozoonoses and bacterial infections
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Nodules on the hair: A rare case of mixed piedra