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Research 211–240 of 1000+
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- Loose anagen hair syndrome
- Hair loss in infancy and childhood
- Short anagen hair with persistent synchronized pattern of scalp hair growth
- The Effect of Parathyroid Hormones on Hair Follicle Physiology: Implications for Treatment of Chemotherapy-Induced Alopecia
- Physiology and Medical Treatments for Alopecia
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Unruly hair
- Hair Shaft Dysplasias
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- Diagnosis and management of hair loss in children
- Melanocytes and Vitiligo (and Hair Graying)
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- The inheritance of common baldness: Two B or not two B ?
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Keratins: the hair shaft's backbone revealed
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Keratin gene mutations in disorders of human skin and its appendages
- Hypotrichosis in a child with olmsted syndrome
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Pachyonychia congenita: Sporadic onset with mutation analysis