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- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Congenital hair loss disorders: Rare, but not too rare
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- AN UPDATE OF HAIR SHAFT DISORDERS
- Disorders of hair in children
- Trichoscopy in hair disorders in darker skin: An approach to diagnosis
- Polarized microscopy in genetic hair disorders: case series
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Hair loss disorders in domestic animals
- Hair and nail disorders
- A polarizing light microscopy can be an easy and reliable diagnostic tool of congenital keratinizing disorders including Netherton syndrome
- PATHOGENESIS OF GENETIC HUMAN HAIR DISORDERS
- Hair biology and hair loss disorders: An update and new concepts
- Genetic hair and nail disorders
- Cholesterol homeostasis: Links to hair follicle biology and hair disorders
- Methods of hair loss evaluation in patients with endocrine disorders.
- Hair and nail disorders of childhood
- Hair Disorders
- Glucocorticoids and mineralocorticoids in hair: facilitating accurate diagnosis of adrenal-related endocrine disorders
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hair Loss in Children
- Hair follicles and their role in skin health
- Clinical relevance of hair microscopy in alopecia
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Hair Loss in Children
- The hair in childhood and old age
- Woolly hair generalizado: caso clínico e revisão da literatura
- Congenital atrichia and hypotrichosis