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Research 271–300 of 1000+
- The aetiology and pathogenesis of alopecia areata
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Prunus mira Koehne in Sichuan, China: Recorded History as a Medicine and Food, Modern Applications, Distribution, and Ethnobotanical Investigations
- Abstracts
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- A Comprehensive Review of GWASs of Human Hair Traits
- Pathological Skin Scarring: From Mechanism to Targeted Local Therapy
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Differences in Demographic and Clinical Characteristics Among Subtypes of Female Pattern Hair Loss
- Pathogenesis of androgenetic alopecia
- Uncombable hair syndrome and beyond
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Androgenic alopecia and dutasteride in hair mesotherapy: A short review
- Biotinidase deficiency characterized by skin and hair findings
- Editorial: Animal fibers
- Viewpoint 2
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries
- Endocrine Influences on Hair Growth
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Woolly Hair in Two Siblings
- Alopecia and its medical management