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n. epidermólisis, descamación de la piel.
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5% after announcing Monday that it plans to file an IND for lead candidate KB103, a treatment for dystrophic epidermolysis bullosa later this month.
M2 PHARMA-February 28, 2018-TWi biotechnology to Begin Phase 2 Clinical Trial of AC-203 for Treatment of Inherited Epidermolysis Bullosa
TRANSPLANTATION of transgenic epidermal cultures successfully created a new, functional epidermis for a boy suffering from junctional epidermolysis bullosa.
James has Epidermolysis Bullosa (EB), a group of genetic skin conditions which cause the skin to blister and tear at the slightest touch.
The top-line data from the trial has indicated that the novel topical wound-healing agent, SD-101, failed to meet the expected endpoints in patient with epidermolysis bullosa.
org/) Epidermolysis Bullosa Medical Research Foundation , (http://people.
Key Words: Epidermolysis bullosa, Blisters, Dental caries, Treatment, Fluoride applications.
EB-101 is the Company's lead gene therapy program for patients suffering with recessive dystrophic epidermolysis bullosa (RDEB), a severe form of epidermolysis bullosa (EB), a group of devastating, life-threatening genetic skin disorders impacting children that is characterized by skin blisters and erosions all over the body.
Global Markets Direct's, 'Epidermolysis Bullosa - Pipeline Review, H1 2016', provides an overview of the Epidermolysis Bullosa pipeline landscape.
INTRODUCTION: Epidermolysis bullosa simplex (EBS) is a group of hereditary bullous diseases characterized by intraepidermal blistering due to mild mechanical traumas.
USPRwire, Thu Jul 30 2015] Global Markets Direct's, 'Epidermolysis Bullosa - Pipeline Review, H1 2015', provides an overview of the Epidermolysis Bullosa's therapeutic pipeline.
Epidermolysis Bullosa (EB) is a heterogeneous group of diseases characterized by a genetic defect of the anchoring proteins between the epidermis and the dermis and can be inherited either autosomal recessively or autosomal dominant.

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