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Research 301–330 of 1000+
- <i>Acorus calamus</i>: a bio-reserve of medicinal values
- Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
- Primary cicatricial alopecia and inflammatory bowel disease – is there a link?
- Nickel Oxide Nanoparticles via Green Synthesis: Insights into Antimicrobial, Antifungal and Dye Degradation Potentials
- Clinical case of a patient with progressive supranuclear palsy – from symptom to diagnosis
- AB1511 SLE ONSET POST COVID-19 VACCINATION: COINCIDENTAL OR ASSOCIATION?
- Advances in Dermatology
- Hair Replacement. Dow B. Stough and Robert S. Haber. St. Louis: Mosby, 1995. 448 pages. Price $189.00.
- Morpho-Regulation of Ectodermal Organs
- Hair Shafts in Trichoscopy
- Cutaneous manifestations of HIV infection other than Kaposi's sarcoma: Clinical and histologic aspects
- Diagnosis and Management of Alopecia in Children
- Endocrine-skin interactions
- Congenital hypotrichosis due to short anagen
- Viral-Associated Trichodysplasia of Immunosuppression
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- Hypertensive crisis associated with St. John’s Wort
- WISP-1 induced by mechanical stress contributes to fibrosis and hypertrophy of the ligamentum flavum through Hedgehog-Gli1 signaling
- Canine noninflammatory alopecia: a comprehensive evaluation of common and distinguishing histological characteristics
- Hair-Thread Tourniquet Syndrome: A Case Report and Literature Review
- Aging in the Male Face: Intrinsic and Extrinsic Factors
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Secondary cicatricial and other permanent alopecias
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- Hair loss
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate