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Research 301–330 of 1000+
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- METHOTREXATE FOR GENERALIZED PUSTULAR PSORIASIS IN A 2-YEAR-OLD CHILD
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Cicatricial alopecia
- A use-and-transformation model for evaluating public R&D: Illustrations from polycystic ovarian syndrome (PCOS) research
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- The Contribution of Endogenous and Exogenous Factors to Female Alopecia
- Síndrome do nevo de Becker
- Clinical Approach to the Patient With Alopecia
- Evaluation of hair loss
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Epigenetic regulation in adult stem cells and cancers
- Female Adolescent Hair Disorders
- Secondary cicatricial and other permanent alopecias
- Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene on Fibre Traits in Inner Mongolia Cashmere Goats
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Hair Shaft Dysplasias
- Primary Cicatricial Alopecias
- Genetic basis of polycystic ovary syndrome
- Frontal Fibrosing Alopecia: Update and Review of Challenges and Successes
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Polycystic Ovarian Syndrome in Adolescents
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Congenital adrenal hyperplasia