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Research 481–510 of 1000+
- Regulation of melanocyte stem cell behavior by the niche microenvironment
- Lymphomatoid granulomatosis
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Ulcerative colitis and total alopecia in a mother and her son
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Evaluation of hair loss
- Androgenetic alopecia; drug safety and therapeutic strategies
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- The Enigma of the Stigma of Hair Loss: Why is Cancer-Treatment Related Alopecia so Traumatic for Women?
- Female Adolescent Hair Disorders
- Postmenopausal virilization after spousal use of topical androgens
- HAIR MATRIX CELL KINETICS: A SELECTIVE REVIEW
- A Single-Centre, Randomized, Double-Blind, Placebo-Controlled Clinical Trial to Investigate the Efficacy and Safety of Minoxidil Topical Foam in Frontotemporal and Vertex Androgenetic Alopecia in Men
- Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles
- Hair Tourniquet Syndrome of the Toe: Report of 2 New Cases
- A Case of Kerion Celsi Caused by Microsporum gypseum (Arthroderma gypseum ) in a Child
- Case 21-2012
- Congenital adrenal hyperplasia
- Hair follicle development and related gene and protein expression of skins in Rex rabbits during the first 8 weeks of life
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Biotinidase deficiency characterized by skin and hair findings
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Carboxytherapy in Aesthetic Medicine
- Out/Performing Our Selves: Invitation for Dialogue
- 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
- Familial frontal fibrosing alopecia: A cross‐sectional study of 20 cases from nine families
- Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability