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Research 241–270 of 1000+
- Loose anagen hair syndrome: Treatment with systemic minoxidil characterised by marked hair colour change
- Role of caffeine in the management of androgenetic alopecia
- Full investigation of patients with polycystic ovary syndrome (PCOS) presenting to four different clinical specialties reveals significant differences and undiagnosed morbidity
- Androgen excess: a hallmark of polycystic ovary syndrome
- Premature graying of hair
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Epidemiological and investigative study of premature graying of hair in higher secondary and pre-university school children
- CLINICAL UPDATES IN HAIR
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Loose Anagen Hair Syndrome in Black‐Haired Indian Children
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology
- Creatine phosphokinase levels and isotretinoin therapy
- Delving into diversity: exploring different risk factors of premature greying of hair
- Diabetes, ovarian tumor, hyperparathyroidism, and papillary cancer: A chance association?
- Hormonal Control of Cardiac Action Potential Phase 1 Currents in the Brugada Syndrome
- Adams–Oliver syndrome: new evidence in variable expressivity?
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- LAMELLAR ICHTHYOSIS: ONE CASE REPORT
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- HAIR REGROWTH
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- The Effect of Plasma Rich in Growth Factors on Pattern Hair Loss: A Pilot Study
- Androgens and hair loss