Search
for
Sort by
Research 30 of 1000+
- Lash Ptosis in Congenital and Acquired Blepharoptosis
- Ptosis in childhood
- Congenital ptosis repair with a frontalis silicon sling: comparison between Fox's single pentagon technique and a modified Crawford double triangle technique
- Changes in eyebrow position following blepharoptosis surgery
- Congenital ptosis: Long-term outcome of frontalis suspension using autogenous temporal fascia or fascia lata in children
- Two different techniques for frontalis suspension using Gore-Tex to treat severe congenital ptosis
- Diseases of Periocular Hair
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- The Endoscopic Brow Lift
- 46,XY DSD due to impaired androgen production
- Myotonic Dystrophy—A Progeroid Disease?
- Periorbital facial rejuvenation; applied anatomy and pre-operative assessment
- Cosmetic Treatment Using Botulinum Toxin in the Oral and Maxillofacial Area: A Narrative Review of Esthetic Techniques
- Plastic surgery : indications, operations, and outcomes
- From Eye Care to Hair Growth: Bimatoprost
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
- An Update of Congenital Adrenal Hyperplasia
- Methimazole, Carbimazole, and Congenital Skin Defects
- Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- 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.
- Management of congenital ichthyoses: European guidelines of care, part two
- Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions