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Junctional Epidermolysis Bullosa

Known as: EPIDERMOLYSIS BULLOSA, GENERALIZED ATROPHIC BENIGN, GABEB, Epidermolysis Bullosa, Junctional [Disease/Finding] 
Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is… 
National Institutes of Health

Papers overview

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2006
2006
Currently, computed tomography is the method of choice for assessment of paranasal sinuses, nasal fossae and their anatomical… 
2003
2003
The mutation responsible for Junctional Epidermolysis Bullosa (JEB) in Belgian draft horses in North America and other draft… 
1990
1990
Keratinocytes from a 1‐week‐old male infant with junctional epidermolysis bullosa letalis (JEBL) were grown in vitro and then… 
Review
1987
Review
1987
The anaesthetic management of two children with junctional epidermolysis bullosa, formerly called the letalis form, is described… 
1983
1983
Junctional epidermolysis bullosa (JEB) is a recessively inherited mechanobullous disease characterized by neonatal onset of… 
1981
1981
Die EBA-Diagnose stutzt sich auf folgende Kriterien: Das klinische Bild ist dem der Epidermolysis bullosa hereditaria… 
1979
1979
The clinical symptomatology of epidermolysis bullosa atrophicans generalisata gravis (Herlitz’ disease), epidermolysis bullosa… 
1954
1954
EPIDERMOLYSIS bullosa is a chronic hereditary condition of the skin and/or mucous membranes, characterized by the development at… 
1947
1947
THE CLINICAL history and the observations at necropsy of a 7 week old white girl afflicted with the rare disease epidermolysis…