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Research 31–60 of 1000+
- Comparative study of the efficacy and safety of topical minoxidil 2% versus topical bimatoprost 0.01% versus topical bimatoprost 0.03% in treatment of eyebrow hypotrichosis: a randomized controlled trial
- Sparse hair in a female toddler
- People’s experiences of eyebrow transplantation: A qualitative study
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Redução da região frontal com incisão pré-capilar: relato de experiência e indicações
- Follicular unit extraction combined with fractional carbon dioxide laser therapy for post‐traumatic eyebrow scar with defects: A prospective and comparative study
- Atomoxetine-Associated Eyebrow Alopecia in a Girl With Attention-Deficit/Hyperactivity Disorder
- A Novel Methodology for Correction of Cosmetic Problems via Secondary Eyebrow Transplantation
- Safety and Efficacy of Bimatoprost Solution 0.03% Topical Application in Patients with Chemotherapy-Induced Eyelash Loss
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Killing Two Birds with One Stone: Oral Tofacitinib Reverses Alopecia Universalis in a Patient with Plaque Psoriasis
- The Latest Innovations in Hair Transplantation
- Diagnostic and Therapeutic Assessment of Frontal Fibrosing Alopecia
- Repair of a Complex Forehead Defect Involving the Brow
- Eyebrow and Eyelash Transplantation Using Chalazion Forceps (Dr. Min’s Method) and Importance of Post-Transplant Recovery in Hair Restoration
- Bimatoprost Can Increase Growth and Density of Eyebrow Hair: A Prospective Study on a Group of Young Women
- Lucio Phenomenon mimicking with Vasculo necrotic Erithema Nodosum Leprosum: A Case Report
- Follicular Unit Extraction (FUE) Hair Transplantation
- Frontal fibrosing alopecia: a survey in 16 patients
- Post Herpetic Itch Leading to Frictional Alopecia of Eyebrow and Scalp-A Hitherto Undescribed Phenomenon
- Isolated hair loss on the eyebrow: five cases with trichoscopic features
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome