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Research 391–420 of 1000+
- 9 Role of 5α-reductase in health and disease
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Calcium in Root Hair Growth
- Potential Causal Relationship Between Extensive Lipid Profiles and Various Hair Loss Diseases: Evidence From Univariable and Multivariable Mendelian Randomization Analyses
- Uso de la espironolactona en dermatología: acné, hidradenitis supurativa, alopecia femenina e hirsutismo
- Diseases of Hair
- Diseases of Hair
- Molecular Genetics of Human Hair Diseases
- Residual antibacterial activity of canine hair treated with five mousse products against<i>Staphylococcus pseudintermedius in vitro</i>
- Factores asociados a alopecia no cicatricial en mujeres adultas, estudio transversal entre enero diciembre 2013
- Diagnosis and treatment of polycystic ovarian syndrome: an update
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Analytical method for the biomonitoring of bisphenols and parabens by liquid chromatography coupled to tandem mass spectrometry in human hair
- One-touch embeddable microneedles for hair loss treatment
- Polyphenol–Inorganic Sulfate Complex-Enriched Straightening Shampoo for Reinforcing and Restoring Reduced Hair Integrity
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Melasma and other skin manifestations or oral contraceptives.
- Pili Trianguli et Canaliculi Is a Defect of Inner Root Sheath Keratinization
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Re‐Innovation in Clinical Trial Designs Based on Precision Therapy
- New clinico‐genetic classification of trichothiodystrophy
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Congenital atrichia associated with nevus flammeus: A rare association
- Successful treatment of a scalp arteriovenous malformation with ulcerative hemorrhage and localized alopecia.
- Fetal gender: preferences, predictions, and its impact on women's sexuality, physical activity, and well-being during pregnancy