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Research 841–870 of 850
- A diagnostic clue: New onset alopecia sparing white hairs
- An Updated in the Management of Alopecia Areata
- Granuloma annulare with alopecia areata in a 6-year-old girl: a case report
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Dermoscopy of annular elastolytic giant cell granuloma
- Trichoscopic findings in various alopecias at tertiary referral center: A cross-sectional study
- Essential syphilitic alopecia: Non-scarring alopecia in 21-year-old man
- Medical Treatment of Alopecia
- Age-Induced Hair Graying and Oxidative Stress
- Oral Presentations
- Atypical bilateral hyperpigmented macules on the lower legs possibly due to cyclophosphamide.
- Bloom's syndrome–‐a first report from India
- Acquired localized hypertrichosis.
- Linear lichen planus pigmentosus of the face with histological findings of lichen planopilaris - an uncommon variant of lichen planus
- Post-laser hair removal folliculitis: A case report
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Sarcoidosis: Are there differences in your skin of color patients?
- Co-occurrence of Progressive Hemifacial atrophy due to Morphea with homolateral segmental Vitiligo: a case report
- Pityriasis versicolor on the scalp: An unusual distribution of a common disease
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Mucocutaneous Manifestations of Endocrine Disorders
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Solar-Induced Postinflammatory Hyperpigmentation after Laser Hair Removal
- A Filipino with Systemic Lupus Erythematosus-Scleroderma Overlap Syndrome
- Phylloid terminal hair nevus: A unique clinical entity
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Pigmentary Puzzle: A Rare Case of Hyperpigmented Cutaneous Sarcoidosis
- FOX FORDYCE DISEASE IN A PREPUBERTAL GIRL