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Research 511–540 of 1000+
- <i>WNT10A</i> , dermatology and dentistry
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Novel agents for the treatment of alopecia
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Congenital adrenal hyperplasia
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Monilethrix Treated with Minoxidil
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Hair transplantation surgery
- Hair and Nail Relationship
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Review paper The use of reflectance confocal microscopy in selected inflammatory skin diseases
- Curcumin derivatives inhibit testicular 17β-hydroxysteroid dehydrogenase 3
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Trichoscopy findings in loose anagen hair syndrome: rectangular granular structures and solitary yellow dots
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Genetics of Structural Hair Disorders
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Congenital atrichia and hypotrichosis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Alopecia - the search for novel agents continues
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Efficacy and Safety of Long-Pulsed 755-nm Alexandrite Laser for Keratosis Pilaris: A Split-Body Randomized Clinical Trial