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Research 91–120 of 1000+
- Disseminated Small Papules on the Face: A Quiz
- PA13 A hair’s breadth from misdiagnosis
- Dermoscopy of discoid lupus erythematosus: Report of two cases
- Yellow dots in trichoscopy: relevance, clinical significance and peculiarities
- Trichoscopy in alopecias
- Widespread and eruptive comedonal lesions with alopecia
- Trichoscopy I: Non-Cicatricial Alopecia
- Dissecting Cellulitis of the Scalp
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Trichoscopic Findings of Erosive Pustular Dermatosis of the Scalp Associated with Gefitinib
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Oestrogen receptor evaluation in Pomeranian dogs with hair cycle arrest (alopecia X) on melatonin supplementation
- Dermoscopic Findings and Their Therapeutic Implications in Trichostasis Spinulosa: A Retrospective Study of 306 Patients
- Current concepts in the pathogenesis and treatment of acne
- [Wooly hair syndrome. Clinical and microscopic study].
- Ichthyosis fetalis in a cross‐bred lamb
- Acquired and inheritedhair disorders
- Clinical diagnosis in canine demodicosis. A new approach.
- Scalp lesions, in images
- Lichen planopilaris
- Olmsted syndrome
- Diffuse hypotrichosis from early childhood
- Validity of trichoscopy in the diagnosis of primary cicatricial alopecias
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Graham‐Little Piccardi Lassueur syndrome and review of the literature
- Trichoscopy of Discoid Lupus Erythematosus in Caucasian Scalp: A Review
- Pruritic Hyperkeratotic Facial Papules
- Graham–Little–Piccardi–Lassueur syndrome: case report and systematic review of a rare LPP variant