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Research 781–810 of 1000+
- Regrowth of black hair in two red‐haired alopecia areata patients
- Hypertrichosis lanuginosa acquisita associated with autoimmune hepatitis
- Signal integrator function of CXXC5 in Cancer
- Response to Falotico et al’s “Biotin beware: Perils of biotin supplementation”
- Molecular basis of androgen insensitivity
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- Acquired hypertrichosis lanuginosa: Case report and review of the literature
- Ichthyosis follicularis with alopecia and photophobia syndrome with coexisting palmoplantar keratoderma treated with acitretin
- P448: Identification of a novel RPS6KA3 variant in a female child with features of Coffin-Lowry syndrome: A case study
- Perspectives of Kennedy's disease
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Polymorphism of genes in patients with new coronavirus infection COVID-19
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Airway Involvement in Conradi–Hünermann–Happle Syndrome: A Novel Clinical Manifestation
- Clinicopathologic and trichoscopic features of keratosis follicularis spinulosa decalvans: A case series study
- Ichthyosis Follicularis with Alopecia and Photophobia Syndrome (IFAP): A Case Report and Review of the Literature
- Soft-tissue calcification in systemic lupus erythematosus
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Cutaneous manifestations associated with substance use disorders
- Close Shave for a Keratin Disorder—K6hf Polymorphism Linked to Pseudofolliculitis Barbae
- Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria
- Low serum testosterone is associated with an increased risk of first-time renal calculi in men without testosterone replacement therapy
- Conditional Gene Expression in the Epidermis of Transgenic Mice Using the Tetracycline-Regulated Transactivators tTA and rTA Linked to the Keratin 5 Promoter
- Feline lymphangiosarcoma – definitive identification using a lymphatic vascular marker