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Research 421–450 of 784
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Clinical picture, diagnosis, treatment and outcome of severe acute respiratory syndrome (SARS) in children
- Update on hidradenitis suppurativa: connecting the tracts
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Distinct transcriptomic landscapes of cutaneous basal cell carcinomas and squamous cell carcinomas
- Mammalian target of rapamycin complex 1 (mTORC1) may modulate the timing of anagen entry in mouse hair follicles
- Loose anagen hair.
- Pathogenesis in pili torti: morphological study
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Cronkhite–Canada syndrome: from clinical features to treatment
- Cronkhite-Canada Syndrome (CCS)—A Rare Case Report
- Ptosis in childhood
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Pili annulati with fragility: Electron microscopic findings of a case
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- Eruptive vellus hair cyst: An uncommon and underdiagnosed entity
- Stereotactic Body Radiation Therapy As a Derivative of Stereotactic Radiosurgery: Clinically Independent But With Enduring Common Themes
- Diagnostic delay, comorbid hidradenitis suppurativa and the prognostic value of bacterial culture in folliculitis decalvans: A cohort study
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- Adult-onset Satoyoshi syndrome in a young male
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome
- SARS-CoV-2 Infection and Alpha-Synucleinopathies: Potential Links and Underlying Mechanisms
- Quantitative analysis of 34 sex (pro)hormones, conjugates and bioactive oxidation products thereof in human plasma by GC- and LC-MS/MS and systematic investigation of overestimations of analyte concentrations not accounted for by method validation
- Multisystemic eosinophilic epitheliotropic disease in a horse in Brazil
- Congenital triangular alopecia: Is it always confined to fronto-temporal region?
- Varying Presentation of Type 1 Polyglandular Failure in India
- Primary TSC2-/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model