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Research 361–390 of 1000+
- Congenital hair loss disorders: Rare, but not too rare
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Shorter CAG repeats in the androgen receptor gene may enhance hyperandrogenicity in polycystic ovary syndrome
- The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- 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
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- A 10 Mb duplication in chromosome band 5q31.3–5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Spontaneous fertility in a male patient with testotoxicosis despite suppression of FSH levels
- ESGCT and FSGT Collaborative Congress Helsinki, Finland September 17–20, 2015 Abstracts
- A smart deoxyribozyme-based fluorescent sensor for in vitro detection of androgen receptor mRNA
- AVALIAÇÃO DA CRIPTOSPORIDIOSE EM CÃES E SUAS IMPLICAÇÕES NA SAÚDE ÚNICA
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- 195 Androgen action and 3D culture conditions influence dermal papilla cells inductive properties: the role of Wnt agonists/antagonists balance
- 196 The endocannabinoid tone regulates human sebocyte biology
- 194 An underlying mechanism of hair loss in acrodermatitis enteropathica
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- 15. Hair and Nails
- Australasian Society for Dermatology Research Meeting, May 2007
- British Society for Dermatopathology: Summaries of Papers
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Alopecia Areata. Current situation and perspectives