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Research 661–690 of 1000+
- Trichoscopy in alopecias: Diagnosis simplified
- Follicular Transplantation
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Update on detection, morphology and fragility in pili annulati in three kindreds
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Trichoscopy
- The nude gene and the skin
- "Curly" Wood and Tiger Tails
- Propranolol induced alopecia
- Trichoscopic findings of androgenetic alopecia and their association with disease severity
- Trichoscopic signs in systemic lupus erythematosus: a comparative study with 109 patients and 305 healthy controls
- Development and Prospects of Organ Replacement Regenerative Therapy
- Cutaneous Ultrastructural Features of the Flaky Skin (<i>fsn</i>) Mouse Mutation
- Histological and dermatoscopic description of sphynx cat skin
- Pathogenesis in pili torti: morphological study
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Efficacy and safety of very-low-dose oral minoxidil 1.25 mg in male androgenetic alopecia
- Traction Alopecia in Two Adolescent Sikh Brothers-An Underrecognized Problem Unmasked by Migration
- The usefulness of dermoscopy in canine pattern alopecia: a descriptive study
- Characterization and causal investigations of an alopecia syndrome in Australian fur seals (<i>Arctocephalus pusillus doriferus</i>)
- An ultrastructural study on corkscrew hairs and cigarette‐ash‐shaped hairs observed by dermoscopy of tinea capitis
- The Study on Biological Function of Keratin 26, a Novel Member of Liaoning Cashmere Goat Keratin Gene Family
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Pili annulati with fragility: Electron microscopic findings of a case
- Trichomycosis (trichobacteriosis) axillaris
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Is thyrotropin-releasing hormone a novel neuroendocrine modulator of keratin expression in human skin?
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Trichoscopic patterns of nonscarring alopecia's