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- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Familial congenital generalized hypertrichosis
- A new type of pachyonychia congenita.
- Fibroblast bioelectric signaling drives hair growth
- Congenital hair loss disorders: Rare, but not too rare
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Female Adolescent Hair Disorders
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Ectodermal Dysplasia: Variable Expressions
- Congenital atrichia and hypotrichosis
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Disorders of hair in children
- Polarized microscopy in genetic hair disorders: case series
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Cantú syndrome with coexisting familial pituitary adenoma
- Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- METHOTREXATE FOR GENERALIZED PUSTULAR PSORIASIS IN A 2-YEAR-OLD CHILD
- Congenital adrenal hyperplasia
- Genetics of Structural Hair Disorders
- Diseases of Periocular Hair
- Biology and Genetics of Hair
- HAIR AND SYSTEMATIC DISEASE
- Inherited Disorders of the Hair
- Secondary cicatricial and other permanent alopecias