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Research 451–480 of 787
- Netherton Syndrome
- Netherton Syndrome
- 075 Clinical investigation of JAK inhibitor Tofacitinib in scarring alopecias
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Thyroid hormone action on skin.
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Spectrum of mucocutaneous manifestations in human immunodeficiency virus-infected patients and its correlation with CD4 lymphocyte count
- 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
- 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
- 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
- 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
- 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
- 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
- Diagnosis of common, benign neonatal dermatoses
- Retinoids - new uses and new synthetic agents
- The human keratins: biology and pathology
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features