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Research 61–90 of 1000+
- Diseases of Periocular Hair
- Significance of iron status in hair loss in women
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases
- Atlas of Geriatric Dermatology
- Hair and scalp disorders
- LUPUS ERYTHEMATOSUS AND THE SKIN
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Gene Therapy: Recent Advances and Applications in Dermatology
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Immunological control of skin development: from homeostasis to developmental pathologies
- 1456 Tensor effect of anigozanthos flavidus flower extract: Modulation of tenascin-X to regenerate the skin
- 1458 EMT-inhibiting transcription factor Ovol2 regulates directional cell migration and proliferation in adult skin epithelia
- Description of skin lesions
- Subject Index
- Clinical Management in Psychodermatology
- LITERATURE REVIEW
- Drug-Induced Skin, Nail and Hair Disorders
- The Spectrum of Skin Disease Among Indian Children
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Differential diagnosis of alopetia in children and adolescents
- Vitamins
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Keratins: the hair shaft's backbone revealed
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Skin applications of cannabidiol: sources, effects, delivery systems, marketed formulations and safety
- The molecular basis of human keratin disorders
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13