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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
- 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
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- 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
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- THE PATHOGENESIS OF ALOPECIA AREATA
- Skin disorders in Parkinson’s disease: potential biomarkers and risk factors
- De Novo Production of Dermal Papilla Cells during the Anagen Phase of the Hair Cycle
- Reversible alopecia universalis secondary to PEG-interferon ??-2b and ribavirin combination therapy in a patient with chronic hepatitis C virus infection
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- 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
- <i>WNT10A</i> , dermatology and dentistry
- What does acne genetics teach us about disease pathogenesis?
- Reversible Alopecia Universalis During Treatment with PEG-Interferon and Ribavirin for Chronic Hepatitis C
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Hair regrowth in a male patient with extensive androgenetic alopecia on estrogen therapy