Search
for
Sort by
Research 241–270 of 813
- Successful induction of oral tolerance in Netherton syndrome
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Frontal fibrosing alopecia
- Hair loss
- Psoriatic Alopecia
- Dupilumab in a 9-week-old with Netherton Syndrome Leads to Deep Symptom Control
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Androgenetic alopecia – is contact dermatitis an accelerating factor?
- Unilateral nevoid hyperkeratosis of the nipple and areola in a Saudi female
- A CLINICAL STUDY OF MUCOCUTANEOUS MANIFESTATIONS OF HIV
- Inherited Disorders of the Hair
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- ИСПОЛЬЗОВАНИЕ ПОЛИНУКЛЕОТИДОВ В АНТИВОЗРАСТНОЙ ИНЪЕКЦИОННОЙ КОСМЕТОЛОГИИ С ПОЗИЦИИ ДОКАЗАТЕЛЬНОЙ МЕДИЦИНЫ
- Homoeopathic management of keratosis pilaris with Arsenic Album: A case report
- The Effectiveness of Topical Keratolytics (Alpha Hydroxy Acids/Beta Hydroxy Acids/Urea) in Treating Keratosis Pilaris: A Review of the Literature
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Clinico-etiological and histopathological correlation in erythroderma: In a tertiary care hospital of Eastern Odisha
- Evaluation of Serum Vitamin-D Levels in Patients with Alopecia Areata
- LB1077 Cutaneous responses to systemic iron: A potential role for epidermal turnover in mammalian iron excretion
- LB1081 Three-dimensional imaging of tight junction-network across multiple layers of human epidermis by array tomography using backscattered electron-mode scanning electron microscopy
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Multi-dermatomal unilateral nevus comedonicus along the lines of Blaschko: a rare presentation
- Oral Presentations
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells
- Ischemic onycholysis of the hands
- 9. Immunology and Genetics
- Adverse Reactions to Oral Retinoids An Update