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Research 121–150 of 183
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Paraproteinemic keratopathy: recognizing the ocular significance
- Differential Diagnosis of Headache and Vertigo: Topical Minoxidil Self-medication Should Be Considered
- Migraine and the menopause transition
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Macrophage Activation Syndrome/Secondary Hemophagocytic Lymphohistiocytosis in Adult‐Onset Still's Disease: An Uncommon Initial Presentation in a Young Nepalese Female: A Case Report
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Understanding, recognizing, and managing toxicities of targeted anticancer therapies
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Advice on the safe introduction and continued use of isotretinoin in acne in the U.K. 2010
- Polycystic Ovary Syndrome: A Comprehensive Review of Pathogenesis, Management, and Drug Repurposing
- Genetics of Inherited Ichthyoses and Related Diseases
- Oral isotretinoin for acne
- LabeledIn: Cataloging labeled indications for human drugs
- Madarosis: A marker of many Maladies
- Adverse event reporting of four anti-Calcitonin gene-related peptide monoclonal antibodies for migraine prevention: a real-world study based on the FDA adverse event reporting system
- Eyebrow Loss
- Immediate Effect in the Retina and Choroid after 650 nm Low-Level Red Light Therapy in Children
- The “in’s and outs” of laser hair removal: a mini review
- Hair follicles modulate skin barrier function
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene