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Research 451–480 of 1000+
- New-Onset Gastrointestinal Polyposis
- Phototherapy of androgenetic alopecia with low level narrow band 655-nm red light and 780-nm infrared light
- Low-level laser therapy for treatment of non-inflammatory alopecia
- Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
- Progeroide Syndrome
- Pharmacologic Therapy of Polycystic Ovary Syndrome
- Focal alopecia in the dog
- The role of hair follicles and Edar signalling in cutaneous wound healing
- Hair Follicle Biology and Topical Minoxidil: Possible Mechanisms of Action
- Hypertensive crisis associated with St. John’s Wort
- Canine noninflammatory alopecia: a comprehensive evaluation of common and distinguishing histological characteristics
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Contents
- Low level of high-density lipoprotein cholesterol is solely associated with greater severity of male androgenetic alopecia: A cross-sectional study of Thai population
- Congenital hypotrichosis due to short anagen
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- WISP-1 induced by mechanical stress contributes to fibrosis and hypertrophy of the ligamentum flavum through Hedgehog-Gli1 signaling
- Hair-Thread Tourniquet Syndrome: A Case Report and Literature Review
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- 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
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Symmetrical alopecia in the dog
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment