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Research 61–90 of 1000+
- Anatomical and Dermatologic Manifestations of Estrogen Deficiency in Postmenopausal Women: A Systematic Review
- Hyperaldosteronism and Hyperprogesteronism in a Cat
- In this Issue
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Drug eruptions in dermatology
- Deferasirox, an oral iron chelator, prevents hepatocarcinogenesis and adverse effects of sorafenib
- 9. Immunology and Genetics
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Paraneoplastic alopecia associated with internal malignancies in the cat
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Biotin
- Editor’s picks January 2021
- Skin connective tissue and ageing
- Oral Presentations
- Vitex negundo: A comprehensive review of phytoconstituents, their derivatives, and therapeutic applications
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- JAK inhibition decreases the autoimmune burden in Down syndrome
- JAK inhibition decreases the autoimmune burden in Down syndrome
- Complex Regional Pain Syndrome Type I : measurements and treatment
- Genetics of Structural Hair Disorders
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Dermatologic manifestations of endocrine disorders
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Netherton Syndrome With Trichorrhexis Invaginata “Bamboo Hair” Under Dermoscopy: Case Images
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Holistic approaches to PCOS: Diet, Exercise and Mental well-being.
- Hair shaft disorders
- Woolly Hair in Two Siblings
- Short Anagen Syndrome
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17