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Research 121–150 of 1000+
- The Review on Alopecia Areata : A Comprehensive Review of Pathogenesis, Diagnosis, Clinical Pattern and Remedies
- The Review on Alopecia Areata : A Comprehensive Review of Pathogenesis, Diagnosis, Clinical Pattern and Remedies
- Multiple facial atrophic scars in childhood
- Rothmund‐Thomson syndrome type 2 – a rare cause of chronic wounds
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- THE PATHOGENESIS OF ALOPECIA AREATA
- Alopecias - Practical Evaluation and Management
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Preliminaries
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Madarosis
- Alopecia: possible causes and treatments, particularly in captive nonhuman primates.
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Alopecia areata: What’s new in epidemiology, pathogenesis, diagnosis, and therapeutic options?
- Treatment-resistant Schizophrenia and Global Cortical Atrophy in a Patient with Turner Syndrome
- Structure and Development of the Skin and Cutaneous Appendages
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- THE PATTERN AND CLINICAL PROFILE OF ALOPECIA AREATA. PANORAMIC REVIEW: UPDATE AND ADVANCES ON ETIOPATHOGENESIS, ASSOCIATED FACTORS, DIAGNOSIS, COMPLICATIONS, MANAGEMENT AND PROGNOSIS IN TREATMENT 2023
- Frontal Fibrosing Alopecia – a review and a practical guide for clinicians
- Clinical report of a Holstein's calf with ichthyosis.
- Alopecia areata - probing the deforestation
- Book Reviews
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- Management of autoimmune associated alopecia areata
- Two Incidental Sibling Diagnoses of Netherton Syndrome in Separate Visits: A Case Report
- Exploration of Potential Secondary Plant Metabolites for the Treatment of Alopecia Areata
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- The cat with alopecia