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Research 121–150 of 619
- ACNE
- Oral Retinoids in Dermatology
- Dermatological symptoms and sexual abuse: a review and case reports
- Interventions for morphea
- Atlas of Geriatric Dermatology
- Beyond Clinical Efficacy: A Literature Review on the Safety Challenges of Isotretinoin Therapy
- Líquen plano pilar e alopecia frontal fibrosante: correlação dos achados clínicos e dermatoscópicos com o grau de inflamação do exame histopatológico
- Aldesleukin
- TRICOSCOPIA – ESTRUTURAS TRICOSCÓPICAS E SUA APLICABILIDADE NAS PATOLOGIAS DO CABELO E DO COURO CABELUDO
- Genetic Hair Disorders: A Review
- Dermoscopy in General Dermatology: A Practical Overview
- Advancements and challenges in stem cell transplantation for regenerative medicine
- 9-cis-Retinoic Acid Capsules in the Treatment of AIDS-Related Kaposi Sarcoma
- Systemic-Onset Juvenile Idiopathic Arthritis with unusual Cutaneous Manifestation and peripheral eosinophilia: Case Report
- Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- Intracranial hypertension as the first manifestation of systemic lupus erythematosus: A case report
- Tumor Angiogenesis and Anti-angiogenic Therapy
- Functional Food Nutrients, Redox Resilience Signaling and Neurosteroids for Brain Health
- Clinically Significant Axial Shortening in Myopic Children After Repeated Low-Level Red Light Therapy: A Retrospective Multicenter Analysis
- Topobiology of Human Pigmentation: P-Cadherin Selectively Stimulates Hair Follicle Melanogenesis
- Dermatologic adverse events in pediatric patients receiving targeted anticancer therapies: A pooled analysis
- Current Therapeutic Approaches to Chronic Central Serous Chorioretinopathy
- The Link Between Obesity and the Skin
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Suppression of FGF5 and FGF18 Expression by Cholesterol-Modified siRNAs Promotes Hair Growth in Mice
- Frontal fibrosing alopecia: a disease that remains enigmatic
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Eccrine angiomatous hamartoma
- Cutaneous toxicities of new targeted cancer therapies: must know for diagnosis, management, and patient-proxy empowerment