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Research 31–60 of 1000+
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Levonorgestrel effects on serum androgens, sex hormone–binding globulin levels, hair shaft diameter, and sexual function
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82
- Edar Signaling in the Control of Hair Follicle Development
- Disorders of hair in infants and children other than alopecia
- Follicular Transplantation
- Age‐dependent changes in damage processes of hair cuticle
- Dermoscopy in hair disorders
- Clinicopathological characteristics and treatment outcomes of fibrosing alopecia in a pattern distribution: A retrospective cohort study
- Fabrication and Magnetic Characterization of Cobalt Antidot Arrays: Effect of the Surrounding Continuous Film
- A case of acquired trichorrhexis nodosa after applying new hair spray
- TRICOSCOPIA – ESTRUTURAS TRICOSCÓPICAS E SUA APLICABILIDADE NAS PATOLOGIAS DO CABELO E DO COURO CABELUDO
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Dynamic expression of Runx1 in skin affects hair structure
- Splitting Hairs
- Congenital atrichia and hypotrichosis
- Philosophy and technique in hair restoration surgery
- THERAPEUTIC EVALUATION OF ḤIJAMAH BIL SHART IN QILLAT SH'AR (ANDROGENETIC ALOPECIA): A CASE STUDY WITH UNANI AND BIOMEDICAL INSIGHTS
- Plica neuropathica: Bird's nest under dermatoscope
- Plica polonica: Trichoscopic findings with a brief literature review
- Trichoscopy in alopecias: Diagnosis simplified
- Trichoscopic patterns of nonscarring alopecia's
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- A Clinical Review of Trichorrhexis Nodosa
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- The nude gene and the skin
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia