Staphylococcal Scalded Skin Syndrome in an Adult on Chemotherapy
Dermatopathology, 2014 Staphylococcal scalded skin syndrome is a toxin-mediated, epidermolytic condition that uncommonly affects adults. A 51-year-old man receiving chemotherapy for leukemia presented with a large geographic erosion with superficial sloughing and multiple ...
Jonathan J. Lee +3 more
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The effect of thyme and tea tree oils on morphology and metabolism of Candida albicans [PDF]
, 2014 Members of Candida species cause significant problems in medicine and in many industrial branches also. In order to prevent from Candida sp. development, essential oils are more and more frequently applied as natural, non-toxic, non-pollutive and ...
Dąbrowska, Mariola +3 more
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Neonatal Skin Disorders: A Review of Selected Dermatologic Abnormalities
, 2000 The skin serves many purposes, acting as a barrier to infection, protecting internal organs, contributing to temperature regulation, storing insulating fats, excreting electrolytes and water, and providing tactile sensory input. This article focuses on a
Banta-Wright, Sandra, Campbell, Juliana
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843 Atypical epidermolytic palmoplantar keratoderma is a mild phenotypic variant of epidermolytic ichthyosis: A new proposal from ultrastructural observations and pro-inflammatory cytokine analyses [PDF]
, 2023 O. Ansai +10 more
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Features of cytological picture at multiforme exudative erythema in oral cavity [PDF]
, 2016 Було вивчено цитологічну картину вмісту ерозій у хворих з токсико-алергічною формою мультиформної еритеми в порожнині рота. Було виявлено, що склад клітинних елементів неспецифічний. Гематогенні і гістіогенні клітини в основному незруйновані.
Karpets, L.M. +6 more
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Epidermolytic nevus: An instance of mosaic epidermolytic ichthyosis
Indian Dermatology Online Journal, 2020 Adya, Keshavmurthy A. +3 more
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Exome sequencing identifies a KRT9 pathogenic variant in a Chinese pedigree with epidermolytic palmoplantar keratoderma [PDF]
, 2019 Changxing Li +9 more
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A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis [PDF]
, 2017 Epidermolytic hyperkeratosis (EHK), (bullous congenital ichthyosiform erythroderma), is an autosomal dominant human skin disorder. Recently, we and others have described mutations in keratins 1 and 10 (K1 and K10) in patients with this disease. Structure-
Anton-Lamprecht, Ingrun +7 more
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Epidermolytic Hyperkeratosis -NPS 2 Type
Indian Journal of Dermatology, 2004 A case of bullous congenital ichthyosiform erythroderma (epidermolytic hyperkeratosis or EHK) with some unusual features is described. It was diagnosed in a 6 month old girl with no family history of either EHK or focal lesions suggestive of mosaicism ...
Das Jayanta Kumar
doaj
LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome [PDF]
, 2017 SPINK5, encoding the putative multi-domain serine protease inhibitor LEKTI, was recently identified as the defective gene in the severe autosomal recessive ichthyosiform skin condition, Netherton syndrome (NS). Using monoclonal and polyclonal antibodies,
Al Saati, Talal +14 more
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