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Research 181–210 of 1000+
- Diffuse hypotrichosis from early childhood
- Five SNP variability in male pattern hair loss patients and healthy individuals from Russia
- Przewidywanie cech wyglądu człowieka na podstawie markerów DNA do celów medyczno-sądowych i kryminalistycznych
- Frontal fibrosing alopecia: reflections and hypotheses on aetiology and pathogenesis
- Skin Keratins
- Core Curriculum for Hair Restoration Surgery, Recommended by the International Society of Hair Restoration Surgery (ISHRS)
- Patent Reports
- THE PATHOGENESIS OF ALOPECIA AREATA
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- PCOS: update and diagnostic approach
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Insight into the pathogensis of polycystic ovarian syndrome
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Dermatomyositis Disease in Dogs
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Netherton Syndrome
- Male androgenetic alopecia
- Double-Lined Frontoparietal Scleroderma en coup de sabre
- RNA-seq analysis identifies key genes enhancing hoof strength to withstand barefoot racing in Standardbred trotters
- 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
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Early Exposure to Sexualized Content and Androgenetic Alopecia: Can Culture Shape Our Biology?
- Clinical cases of Darier-White follicular dyskeratosis
- Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
- Adult Onset Isolated Hypogonadotropic Hypogonadism- a Cause of Secondary Amenorrhea
- Symposium Proceedings of the 4th Intercontinental Meeting of Hair Research Societies: “The World of Hair 2004”
- Chronic overlapping pain conditions and nociplastic pain
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing