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- USO DE ESTIMULAÇÃO CEREBRAL PROFUNDA (DBS) PARA O TRATAMENTO DA DOENÇA DE PARKINSON
- Parkinson's disease and skin
- Analysis of Methyltestosterone and Testosterone Propionate in Dried Blood Spots After Transdermal Application
- Evaluation of glucuronide metabolite stability in dried blood spots
- Crusted plaques of the scalp after deep brain stimulation surgery
- Gilles de la Tourette syndrome – A treatable condition?
- A Combinatorial Tweet Clustering Methodology Utilizing Inter and Intra Cosine Similarity
- Quantitative analysis of finasteride tablets dissolution content with non-isotopically labeled internal standard by paper spray ionization mass spectrometry
- Use of a Healthcare Claims Database for Post-Marketing Safety Assessments of Eribulin in Japan: A Comparative Assessment with a Prospective Post-Marketing Surveillance Study
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Scalp needle mesotherapy as a method supporting the treatment of alopecia
- Study on modification of rabbit hair fibers with L-cysteine
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Prediction of male-pattern baldness from genotypes
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Effect of dihydrotestosterone on the upregulation of inflammatory cytokines in cultured sebocytes
- A Clinical Approach to Severe Insulin Resistance
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients