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Research 631–660 of 1000+
- METHOTREXATE FOR GENERALIZED PUSTULAR PSORIASIS IN A 2-YEAR-OLD CHILD
- Genetic and molecular aspects of androgenetic alopecia
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- COVID-19 infection leading to acute pustular dermatoses
- Associations between clinical data, vaccination status, antibody responses, and post-COVID-19 symptoms in Thais infected with SARS-CoV-2 Delta and Omicron variants: a 1-year follow-up study
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Lipedematous Alopecia: Clinical, Histopathological, and Trichoscopic Findings of a Single Case and Review of the Literature
- Debatable Topics in PCOS Patients
- Differences in male and female pattern hair loss based on androgens, estrogen, iron, vitamin D, lipid metabolism, and genetic regulation
- Alopecia and Its homoeopathic treatment
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Genetic diversity and phylogeography of the endemic species Prunus mira in the Qinghai–Tibetan Plateau
- Primary scarring alopecias. A literature review
- ADAM17 variant causes hair loss via ubiquitin ligase TRIM47 mediated degradation
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Cyberspace Chat: Beyond genetics part III: evidence that lifestyle choices may impact hair loss in androgenetic alopecia
- Developmental genetics of color pattern establishment in cats
- Analyzing the role of ACE2, AR, MX1 and TMPRSS2 genetic markers for COVID-19 severity
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- RETRACTED: Explore the genetic exposure to alopecia areata
- MITF E318K naevus phenotype: the modifying role of MC1R Red Hair Variants
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Association of Gly972Arg variant of insulin receptor subtrate-1 and Gly1057Asp variant of insulin receptor subtrate-2 with polycystic ovary syndrome in the Chinese population
- Past, Present and Future Perspectives of Forensic Genetics
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits