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- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- A rare clinical image of hypertrichosis (Werewolf syndrome)
- Fibroblast bioelectric signaling drives hair growth
- Topical cetirizine and oral vitamin D: a valid treatment for hypotrichosis caused by ectodermal dysplasia
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Congenital atrichia and hypotrichosis
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Familial congenital generalized hypertrichosis
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Disorders of hair in children
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Dermatopathology and molecular genetics
- Congenital atrichia associated with nevus flammeus: A rare association
- Polarized microscopy in genetic hair disorders: case series
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Alopezien und Hypotrichosen im Kindesalter
- Effects of Hormones and Endocrine Disorders on Hair Growth
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Cutaneous Granular Cell Tumor with Overlying Hypertrichosis in an Adult: A Rare Case Report
- Brief study of hypertrichosis
- A guide to diagnosis and management of hypertrichosis
- Diseases of Periocular Hair
- Hair physiology and its disorders
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Hair and scalp disorders
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis