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Research 30 of 642
- Clinical and trichoscopic characteristics of temporal triangular alopecia: A multicenter study
- Male fertility and skin diseases
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- Histopathology of non-scarring alopecia
- Primary cicatricial alopecia
- HAIR AND SYSTEMATIC DISEASE
- Do Changes in Chromosomes Cause Aging?
- Increased androgen bioavailability is associated with non-alcoholic fatty liver disease in women with polycystic ovary syndrome
- Alopecia in Cronkhite-Canada syndrome
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Metabolic Syndrome in Androgenetic Alopecia in a Tertiary Care Centre in Goa: A Case Control Study During COVID-19 Pandemic
- From Hair-Pulling to Trichobezoars and Rapunzel Syndrome: A Comprehensive Review of Trichotillomania
- Putative role for insulin resistance in depression risk in polycystic ovary syndrome
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Hair Tourniquet Syndrome of the Toe: Report of 2 New Cases
- Short anagen syndrome in an African American woman
- Hair tourniquet syndrome of toes and fingers in infants
- Polycystic Ovary Syndrome: A Comprehensive Review of Its Clinical Presentation, Comorbidities, Long-Term Complications and Management
- Cancer risk in polycystic ovary syndrome patients: Common treatments and future perspectives
- Pharmakokinetik und Biokonversion von Dehydroepiandrosteron nach Dexamethason-Vorbehandlung bei Frauen mit dem Syndrom der polyzystischen Ovarien
- Characterization and causal investigations of an alopecia syndrome in Australian fur seals (<i>Arctocephalus pusillus doriferus</i>)
- Hair-Thread Tourniquet Syndrome in an Infant With Bony Erosion
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Cronkhite-Canada Syndrome Associated With Superficial Esophageal Carcinoma: A Case Report and Literature Review
- Metabolism and skin diseases
- Cantú Syndrome Is Caused by Mutations in ABCC9
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses