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Research 361–390 of 1000+
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Polycystic ovary syndrome: a complex condition with psychological, reproductive and metabolic manifestations that impacts on health across the lifespan
- Hair growth promoting effects of adipose tissue-derived stem cells
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Frontal fibrosing alopecia
- The great atopic diseases epidemic: does chemical exposure play a role?
- Alopecia in women submitted to childhood X-ray epilation for tinea capitis treatment
- Alopecia universalis after discontinuation of pegylated interferon and ribavirin combination therapy for hepatitis C: a case report
- The hair growth promoting effect of 4-O-methylhonokiol
- Highlights
- Hormonal Control of Cardiac Action Potential Phase 1 Currents in the Brugada Syndrome
- LO-010 Relationship between the EULAR/ACR classification criteria and organ damage in systemic lupus erythematosus
- LO-009 Responsiveness of the CLASI to alopecia and mucous membrane involvement: a retrospective study of prospectively collected data
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- Body composition changes and inhibition of fat development in vivo implicates androgen in regulation of stem cell lineage allocation
- Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- What does acne genetics teach us about disease pathogenesis?
- Tumor Necrosis Factor-Alpha and Polycystic Ovarian Syndrome: A Clinical, Biochemical, and Molecular Genetic Study
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- DNA phenotyping: current application in forensic science
- Fatal Toxic Epidermal Necrolysis Associated with Minoxidil
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population