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Research 631–660 of 1000+
- Asthma
- Platelet-Rich Plasma in the Treatment of Androgenetic Alopecia: An Equation with Many Unknowns
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- COVID-19 pandemic and teledermatology in low-income regions
- Stable Isotopes And Multiple Tissue Analysis: Reconstructing Life Histories For Individuals From Dakhleh Oasis, Egypt
- Transcutaneous electrical acustimulation promotes wound healing in mice by modulating signaling molecules and mitochondria function
- Patterns of Common Dermatological Conditions among Children and Adolescents in Pakistan
- Comparative study of the action of dynamized forms of melatonin and lissotriton
- Skin regeneration with conical and hair follicle structure of deep second-degree scalding injuries via combined expression of the EPO receptor and beta common receptor by local subcutaneous injection of nanosized rhEPO
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Quintaquinone, a Merosesquiterpene from the Yellow Sponge Verongula cf. rigida Esper
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- Heavy Metals: The Notorious Daredevils of Daily Personal Care Products- Mini Review
- Bullous pyoderma gangrenosum occurring on a cesarean section scar
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia
- Highway Deconstruction
- The Dermatologic Care Needs of a Rural Community in South Florida
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- A New CARASIL Family: Recurrent Lobar Hemorrhage as a Novel Characteristic of the Disease
- Recombinant Human Growth Hormone Promotes Burn Wound Repair by Regulating Vascular Endothelial Growth Factor and Micro Vessel Density
- A systematic review on Drug Re-profiling/Re-Purposing
- Human Epidermal Neural Crest Stem Cells (hEPI-NCSC)—Characterization and Directed Differentiation into Osteocytes and Melanocytes
- Dermal Delivery of Topically Applied Oligonucleotides via Follicular Transport in Mouse Skin
- A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population
- Development of ethosome comprising combined herbal extracts and its effect on hair growth
- The arrector pili muscle, the bridge between the follicular stem cell niche and the interfollicular epidermis
- Are Nutraceuticals Effective in COVID-19 and Post-COVID Prevention and Treatment?