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Research 151–180 of 1000+
- A RARE CASE OF CHRONIC ACRODERMATITIS ENTEROPATHICA PERSISTING AND RECURRING IN THE ADULT AGE
- Adams–Oliver syndrome: new evidence in variable expressivity?
- Decades of progressive red and yellow nodules
- Treatment of Hair Loss
- Molecular mechanisms of androgenetic alopecia
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- HAIR REGROWTH
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries
- The Effect of Plasma Rich in Growth Factors on Pattern Hair Loss: A Pilot Study
- Alopecia areata: An update
- Approach to the adult female patient with diffuse nonscarring alopecia
- Review of quality of life studies in women with alopecia
- Hirsutism and the Variable Response of the Pilosebaceous Unit to Androgen
- Oral Manifestations of Hematologic and Nutritional Diseases
- Family History and Risk of Hair Loss
- Biochemical Roles of Testosterone and Epitestosterone to 5α-Reductase as Indicators of Male-Pattern Baldness
- Roles of tumor suppressors in regulating tumor-associated inflammation
- Scalp whorls
- A pilot study evaluating the efficacy of topically applied niacin derivatives for treatment of female pattern alopecia
- In vivo hair growth-promoting efficacies of herbal extracts and their cubosomal suspensions
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Congenital atrichia and hypotrichosis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- 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
- Molecular Genetics of Alopecias
- Focal and Generalized Alopecia