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Research 391–420 of 1000+
- Review of oral minoxidil as treatment of hair disorders: in search of the perfect dose
- Dermatologist‐diagnosed skin diseases among immigrant Latino poultry processors and other manual workers in North Carolina, USA
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Topical minoxidil and tretinoin combined with an oral vitamin D analog as a treatment for woolly hair
- Exuberant tufted folliculitis
- Diagnostic Accuracy of Polarized and Ultraviolet Fluorescence-Induced Dermoscopy in Scarring and Nonscarring Alopecias: a Retrospective Observational Multicentric Study
- Increased expression of psoriasin (S100A7) and interleukin 17 (IL-17) in lesional skin in lichen planopilaris
- Therapeutic Updates on Lichen planopilaris and Frontal Fibrosing Alopecia: A Systematic Review
- Kadın Olgularda Yaygın Saç Kaybı ve Eşlik Eden Bulgular
- Ichthyosis Follicularis With Alopecia and Photophobia
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- A Retrospective Study of Frontal Fibrosing Alopecia from North-East India
- Cicatricial Alopecia
- Erythromelanosis follicularis faciei in women
- ERYTHROMELANOSIS FOLLICULARIS FACIEI ET COLLI
- Value of dermoscopy for the diagnosis of monilethrix
- Absolute Dermatology Review
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Cutaneous disorders related to obesity
- Trichoscopic findings in various alopecias at tertiary referral center: A cross-sectional study
- [Arnozán-Dubreuilh depilating folliculitis].
- A Case of Idiopathic Follicular Mucinosis Treated Successfully with Cyclosporine.
- Erythromelanosis Follicularis Faciei et Colli: A Case Report in a Caucasian Male and Brief Review of the Literature
- Erythromelanosis follicularis faciei et colli with reticulated hyperpigmentation of the extremities
- Trichilemmal cyst of the neck: case report and review of the literature
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes