Search
for
Sort by
Research 91–120 of 122
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Hypotrichosis in a child with olmsted syndrome
- Telogen Effluvium
- Dermoscopic Findings of Alopecia in Patients with Hypothyroidism
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Oral Vitamin D Treatment in Patients with Telogen Effluvium: Clinical and Dermoscopic Evaluation
- Telogen Effluvium: A Review
- Differentiation of frontal fibrosing alopecia and Lichen planopilaris on trichoscopy: A comprehensive review
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management
- The rising burden of alopecia: A review on aetiology, prevalence and role of homoeopathy
- Investigating the potential mechanism of microneedling in alopecia areata mice based on 16S rRNA sequencing and metabolomics
- Repeatable Perming via Thiol–Michael Click Reaction: Using Amide Derived from Maleic Acid and Cystine
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Characteristics of Androgenetic Alopecia in Asian
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Alopecia and Associated Toxic Agents: A Systematic Review
- ASSESSMENT OF SERUM LEVELS OF ANTIGLIADIN ANTIBODIES (IgG and IgA) IN PATIENTS WITH ALOPECIA AREATA AND THEIR RELATION TO SEVERITY OF THE DISEASE
- Therapeutic Efficacy of Combination Therapy Using Oral Cyclosporine with a Dietary Supplement (Pantogar®) in Twenty-Nail Dystrophy
- Ectodermal Dysplasia: Variable Expressions
- Alopecia Areata of the Nails: Diagnosis and Management
- Investigation of dermatological manifestations in maintenance hemodialysis patients
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Approach to Nail Pitting in Pediatric and Adolescent Patients: A Dermatology Perspective
- A clinical study of Geriatric dermatoses at Tertiary care center in South India