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Research 241–270 of 1000+
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Potential Causal Relationship Between Extensive Lipid Profiles and Various Hair Loss Diseases: Evidence From Univariable and Multivariable Mendelian Randomization Analyses
- Polyphenol–Inorganic Sulfate Complex-Enriched Straightening Shampoo for Reinforcing and Restoring Reduced Hair Integrity
- An Updated Etiology of Hair Loss and the New Cosmeceutical Paradigm in Therapy: Clearing ‘the Big Eight Strikes’
- Molecular Genetics of Human Hair Diseases
- Calcium in Root Hair Growth
- Ketoconazole Shampoo: Effect of Long-Term Use in Androgenic Alopecia
- Congenital hypotrichosis due to short anagen
- 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
- Short anagen syndrome
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Hirsutism in the Adolescent Female
- Scalp whorls
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- New clinico‐genetic classification of trichothiodystrophy
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- The Anthropogenic Disappearance of Inorganic Tin (Stannum) as a Hidden Driver of Myocardial Insufficiency and Symmetrical Androgenetic Alopecia: A Novel Pathophysiological Hypothesis
- The Anthropogenic Disappearance of Inorganic Tin (Stannum) as a Hidden Driver of Myocardial Insufficiency and Symmetrical Androgenetic Alopecia: A Novel Pathophysiological Hypothesis
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Congenital atrichia associated with nevus flammeus: A rare association
- Re‐Innovation in Clinical Trial Designs Based on Precision Therapy
- Ceramic flat irons: Improper use leading to acquired trichorrhexis nodosa
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- [The Netherton syndrome with alopecia and prolinuria].
- Oral Presentations