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Research 481–510 of 1000+
- Alopecia: Association with Resistance to Thyroid Hormones
- Pohl-Pinkus constrictions of hair following chemotherapy for Hodgkin's disease
- Artificial Hair: By the Dawn to Automatic Biofibre® Hair Implant
- Alopecias Due to Drugs and Other Skin and Systemic Disorders
- Hair Transplantation in Females
- RECENT DEVELOPMENTS IN ALOPECIAS
- Fibrosing Alopecia in a Pattern Distribution: A Case Report and Literature Review
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Curling of Hair in Two Female Patients Taking Alitretinoin
- The early repigmentation pattern of vitiligo is related to the source of melanocytes and by the choice of therapy: a retrospective cohort study
- Canities subita: sudden blanching of the hair in history and literature
- Hair disorders associated with autoimmune connective tissue diseases.
- Hair-cycle changes in two patients taking tocilizumab
- Skin Manifestations of Hypothyroidism-A Clinical Study
- Recurrent episodes of hair loss in a 37 year old woman
- Acquired Uncombable Hair
- Alopecia and hirsutism*
- An adult case of suspected A20 haploinsufficiency mimicking polyarteritis nodosa
- Female pattern hair loss in men: A distinct clinical variant of androgenetic alopecia
- Familial Androgenetic Alopecia in Siblings with Normal Endocrinological Status
- A practical guide for the treatment of dandruff and seborrheic dermatitis
- Epidemiological, Clinical, and Trichoscopic Features of Syphilitic Alopecia: A Retrospective Analysis and Systematic Review
- Telogen effluvium in the new SARS‐CoV‐2 era
- Diagnosis and Treatment of Nonscarring Hair Loss in Primary Care in 2021
- CDK4/6 plus aromatase inhibitor-induced alopecia in breast cancer patients.
- A tricky case of hair loss in a child: Trichoscopy saves the day
- Eyelash Trichomegaly: A Rare Presenting Feature of Systemic Lupus Erythematosus.
- Telogen effluvium. New possibilities of correction
- Adrenoleukodystrophy: A Rare Case Report
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families