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Research 541–570 of 1000+
- Primary cicatricial alopecia
- Diagnosis and Management of Primary Cicatricial Alopecia: Part I
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- X linked mental retardation.
- Common causes of hair loss – clinical manifestations, trichoscopy and therapy
- Oral Treatment of Keratinizing Disorders of Skin and Mucous Membranes With Etretinate
- Commentary: Darier-White Disease
- Hair Disorders
- Cicatricial Alopecias
- Disorders of Keratinization
- Yellow dots in trichoscopy: relevance, clinical significance and peculiarities
- Trichoscopy I: Non-Cicatricial Alopecia
- Folliculocentric tinea versicolor: a case report
- Adverse cutaneous reactions to the new second-generation tyrosine kinase inhibitors (dasatinib, nilotinib) in chronic myeloid leukemia
- Trichostasis Spinulosa
- Trichostasis Spinulosa
- Disseminated Small Papules on the Face: A Quiz
- Diffuse hypotrichosis from early childhood
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Graham–Little–Piccardi–Lassueur syndrome: case report and systematic review of a rare LPP variant
- Monilethrix: Beaded hair and hypotrichosis in a child
- Olmsted syndrome
- 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
- 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
- Current concepts in the pathogenesis and treatment of acne
- [Wooly hair syndrome. Clinical and microscopic study].
- Ichthyosis fetalis in a cross‐bred lamb