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Research 361–390 of 1000+
- Treatment of erythromelanosis follicularis faciei et colli with a 595‐nm pulsed dye laser
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- GLOMERULAR MEMBRANOUS NEPHROPATHY AND WERNER SYNDROME: A CASE REPORT
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- New Modalities in the Treatment of Refractory Alopecia Areata
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Osseous Metaplasia and Mature Bone Formation With Extramedullary Hematopoiesis in Trichilemmal Cyst
- Evaluation of the Hair Growth-Promoting Effects of Combined Treatment with Hair Growth Stimulants
- Beyond Wavy Hairs
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Trichoscopy in genetic hair shaft abnormalities
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- New developments in the molecular treatment of ichthyosis: review of the literature
- Converging physiological roles of the anthrax toxin receptors
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Vitamin D-Dependent Rickets Type II with Alopecia: A Rare Case Report.
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality