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- Normalization of testosterone levels using a low estrogen-containing oral contraceptive in women with polycystic ovary syndrome.
- Implications of Non-compliance in the Management of Chronic Polycystic Ovarian Syndrome
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Reply
- Hormonal contraceptives: pharmacology tailored to women's health
- Pharmacologic Therapy of Polycystic Ovary Syndrome
- CLINICAL UPDATES IN HAIR
- Steroid Hormones of Reproduction and Sexual Development
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Morphological Approach to Hair Disorders
- Hairless is a nuclear receptor corepressor essential for skin function
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Dermatopathology and molecular genetics
- Congenital atrichia and hypotrichosis
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Le gène<i>hairless</i>de la souris
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- ORLISTAT
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- NEFAZODONE
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.