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Research 61–90 of 1000+
- Eyebrow Loss
- Total Facelift: Forehead Lift, Midface Lift, and Neck Lift
- Toxic and Metabolic Disorders of the Nervous System
- Utilities of Botulinum Toxins in Dermatology and Cosmetology
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Skin Sceneries of Thyroid Disorders and Impact of Thyroid on Different Skin Diseases: A Scoping Review Focused on Pediatric Patients
- Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework
- Aesthetic Medicine and Aesthetic Health Psychology: Toward an Integrative Framework for Patient-Centered Care
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Report on the 11th National Congress AICPE (Associazione Italiana di Chirurgia Plastica Estetica) Held in Rimini, Italy, 12–14 April 2024
- E-Poster
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Chitosan-Based Scaffolds Incorporated with Silver Nanoparticles for the Treatment of Infected Wounds
- Endoscopic assisted facial rejuvenation: a 35 year personal journey
- 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
- Congenital hypotrichosis due to short anagen