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Research 121–150 of 502
- Dermatological Manifestations of Celiac Disease: a Literature Review
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- Contaminants of emerging concern in the fetal environment
- Líquen plano pilar e alopecia frontal fibrosante: correlação dos achados clínicos e dermatoscópicos com o grau de inflamação do exame histopatológico
- Encapsulación en ciclodextrinas de compuestos con actividad frente a la alopecia androgénica masculina.
- 公表学術論文等リスト 2018
- Autoimmune polyglandular syndrome type 4 – case report
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Abstracts Pt.30
- National scientific medical meeting 1996 abstracts
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- COVID-19 and Sex Differences
- Clinical manifestations of cutaneous lupus erythematosus
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Genetic prediction of male pattern baldness
- Hair Follicle Immune Privilege Revisited: The Key to Alopecia Areata Management
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- Adverse effects of common medications on male fertility
- Nonclassic adrenal hyperplasia
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?