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Research 31–60 of 801
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Trichoscopy in Hair Shaft Disorders
- The urine as a diagnostic key for a homozygous EGFR mutation
- Hair loss in infancy and childhood
- Hair Loss in Children
- Oral Presentations
- Endocrine-skin interactions
- Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III
- Skin manifestations of endocrine diseases
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- The Genetics of Human Skin Disease
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Trichodystrophies: A hair-raising differential diagnosis
- Hair Loss in Children
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Ichthyosis with confetti: clinics, molecular genetics and management
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- A guide to diagnosis and management of hypertrichosis
- Acne Syndromes and Mosaicism
- First Symposium of Ichthyosis Experts
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Congenital hair loss disorders: Rare, but not too rare
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Animals in Dermatology
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children