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- Hair Shaft Abnormalities. Pili Bifurcati: A Scanning Electron Microscopy Analysis
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Bubble hair and other acquired hair shaft anomalies due to hot ironing on wet hair
- A case of acquired trichorrhexis nodosa after applying new hair spray
- Central trichoptilosis with onycholysis
- A Clinical Review of Trichorrhexis Nodosa
- Plica polonica: Trichoscopic findings with a brief literature review
- Hair shaft disorders
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Trichorrhexis Nodosa After Hair Transplantation: Dermoscopic, Pathologic and Electron Microscopy Analyses
- Hair shaft disorders in children – An update
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- Congenital atrichia and hypotrichosis
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Fourth Nerve Palsy After Hair Replacement Surgery and Prolonged Vertical Position in a Patient With Mega-Cisterna-Magna: Report of a Case
- The Developmental & Molecular Requirements for Ensuring that Human Pluripotent Stem Cell-Derived Hair Follicle Bulge Stem Cells Have Acquired Competence for Hair Follicle Generation Following Transplantation
- Disorders of hair in infants and children other than alopecia
- Diseases of Periocular Hair
- Hair and Scalp Variation Related to Gender
- Hair physiology and its disorders
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Against the Rules: Human Keratin K80
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Trichoscopy in alopecias: Diagnosis simplified
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Deletion of the epidermis derived laminin γ1 chain leads to defects in the regulation of late hair morphogenesis
- Trichoscopy and Trichogram