"Epidermolysis Bullosa" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties.
Descriptor ID |
D004820
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MeSH Number(s) |
C16.131.831.493 C16.320.850.275 C17.800.804.493 C17.800.827.275 C17.800.865.410
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Epidermolysis Bullosa".
Below are MeSH descriptors whose meaning is more specific than "Epidermolysis Bullosa".
This graph shows the total number of publications written about "Epidermolysis Bullosa" by people in this website by year, and whether "Epidermolysis Bullosa" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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2010 | 1 | 0 | 1 |
2016 | 1 | 0 | 1 |
2017 | 5 | 0 | 5 |
2018 | 2 | 0 | 2 |
2019 | 1 | 0 | 1 |
2020 | 2 | 0 | 2 |
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Below are the most recent publications written about "Epidermolysis Bullosa" by people in Profiles.
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Coronavirus disease 2019 and epidermolysis bullosa: Report of three cases. Dermatol Ther. 2020 Nov; 33(6):e14194.
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Multidisciplinary care of epidermolysis bullosa during the COVID-19 pandemic-Consensus: Recommendations by an international panel of experts. J Am Acad Dermatol. 2020 Oct; 83(4):1222-1224.
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Epidermolysis Bullosa Patients' Perception of Surgical Wound and Scar Healing. Dermatol Surg. 2019 02; 45(2):280-289.
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A review of scoring systems for ocular involvement in chronic cutaneous bullous diseases. Orphanet J Rare Dis. 2018 05 22; 13(1):83.
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Genome-wide single nucleotide polymorphism-based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa. Exp Dermatol. 2019 10; 28(10):1118-1121.
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Wound culture isolated antibiograms and caregiver-reported skin care practices in children with epidermolysis bullosa. Pediatr Dermatol. 2018 Jan; 35(1):92-96.
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Diagnosis of Inherited Epidermolysis Bullosa in Resource-Limited Settings: Immunohistochemistry Revisited. Dermatology. 2017; 233(4):326-332.
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Erosive pustular dermatosis of the scalp and Kindler syndrome: a new association. J Eur Acad Dermatol Venereol. 2018 Mar; 32(3):e102-e104.
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Pro-Inflammatory Chemokines and Cytokines Dominate the Blister Fluid Molecular Signature in Patients with Epidermolysis Bullosa and Affect Leukocyte and Stem Cell Migration. J Invest Dermatol. 2017 11; 137(11):2298-2308.
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High concordance between clinical diagnosis of epidermolysis bullosa and immunofluorescence with a small, well-matched antibody panel. Australas J Dermatol. 2018 Feb; 59(1):73-76.