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Research 61–90 of 1000+
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Male sex hormone and reduced plakoglobin jointly impair atrial conduction and cardiac sodium currents
- Updated Management of Atrophic Post Acne Scars: Review Article
- Combined treatment modalities in atrophic acne scars: a prospective study
- ATRICHIA WITH PAPULAR LESIONS – A CASE REPORT
- Atrophying scamous papulous dermatitis (Degos disease): Nine years of follow-up
- Topical Delivery of Atraric Acid Derived from Stereocaulon japonicum with Enhanced Skin Permeation and Hair Regrowth Activity for Androgenic Alopecia
- Hyaluronate Fragments Reverse Skin Atrophy by a CD44-Dependent Mechanism
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- 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.
- Targeted Skin Overexpression of the Mineralocorticoid Receptor in Mice Causes Epidermal Atrophy, Premature Skin Barrier Formation, Eye Abnormalities, and Alopecia
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Generalized atrophic benign epidermolysis bullosa.
- Skin physiology in microgravity: a 3-month stay aboard ISS induces dermal atrophy and affects cutaneous muscle and hair follicles cycling in mice
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Cutaneous Atrophy and Alopecia After Greater Occipital Nerve Injection Using Triamcinolone
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Minoxidil: right atrial cardiac pathology in animals and in man.
- Erosive pustular dermatosis (chronic atrophic dermatosis of the scalp and extremities)
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Perilymphatic Atrophy of the Skin
- Finasteride-mediated hair regrowth and reversal of atrophy in a patient with frontal fibrosing alopecia
- Epithelial Cells in the Hair Follicle Bulge do not Contribute to Epidermal Regeneration after Glucocorticoid-Induced Cutaneous Atrophy
- The Safety of Local Hormonal Treatment for Vulvovaginal Atrophy in Women With Estrogen Receptor-positive Breast Cancer Who Are on Adjuvant Aromatase Inhibitor Therapy: Meta-analysis
- Molecular basis of congenital atrichia in humans and mice.
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Trichoscopy of Steroid-Induced Atrophy
- Congenital atrichia and hypotrichosis
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families