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Research 451–480 of 1000+
- A rare case of woolly hair with unusual associations
- Dermoscopy: A rapid bedside tool to assess monilethrix
- TRICHOSTASIS SPINULOSA OR PINSELHAAR
- Punctate Follicular Porokeratosis
- Atrichia with papular lesions
- Traumatic anserine folliculosis
- Follicular porokeratosis: four new cases
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Winer's dilated pore, rare presentation in the external ear canal
- Fox-Fordyce disease. Control with tretinoin cream
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>
- [Perforating folliculitis].
- Kératose pilaire
- Trichoscopy in alopecias
- Discreet monilethrix: De novo mutation on the example of polish families
- Atrichia with papular lesions in Syrian siblings exposing global diagnostic challenges in genetic alopecia: A rare case report
- A prospective descriptive study of 100 patients with facial trichostasis spinulosa
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Skin iconography analysis of traumatic anserine folliculosis: Skin image feature of TAF
- Multifocal alopecia of the scalp, axillae, and body
- Multiple facial atrophic scars in childhood
- Reflectance Confocal Microscopy of Adult Periorificial Dermatitis: A Case Report
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Widespread and eruptive comedonal lesions with alopecia
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Trichoscopy I: Non-Cicatricial Alopecia
- Sparse Hair on the Scalp
- Hypotrichosis in a child with olmsted syndrome
- A rare hair loss in children: Monilethrix
- Moniletherix