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Research 61–90 of 1000+
- Bimatoprost Can Increase Growth and Density of Eyebrow Hair: A Prospective Study on a Group of Young Women
- Bimatoprost in the treatment of eyelash hypotrichosis
- Madarosis
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Jarilla–Coffea extract: a natural cosmetic product that improves eyelash and eyebrow growth in women
- Disorders of hair in children
- Dr Shoji Okuda (1886-1962): The great pioneer of punch graft hair transplantation
- Eyebrow Regrowth in Patients with Frontal Fibrosing Alopecia Treated with Low-Dose Oral Minoxidil
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Successful use of bimatoprost in the treatment of alopecia of the eyelashes
- Vorasidenib-Induced Trichomegaly and Hypertrichosis: a New Side Effect in a Patient with Diffuse Astrocytoma
- Comparison of minoxidil sulfotransferase activity between scalp hair, eyebrows, and eyelashes: Implication for minoxidil efficacy for off‐label use
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Minoxidil-induced hypertrichosis in a child with alopecia areata
- Phosphodiesterase inhibitors and prostaglandin analogues in dermatology: A comprehensive review
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Novel Application of Light-Emitting Diode Therapy in the Treatment of Eyebrow Loss in Frontal Fibrosing Alopecia
- Comparative evaluation of eyebrow rejuvenation using hibiscus oil 5% (w/v) with and without Gua-sha: A split face randomized control Trial
- Diffuse face and ear hypertrichosis caused by 5% topical minoxidil in an adult woman with spontaneous resolution
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hair physiology and its disorders
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Hypotrichosis with juvenile macular dystrophy