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An International Online Survey on Oral Hygiene Issues in Patients with Epidermolysis Bullosa. [PDF]
Dent J (Basel)Garuti G +5 more
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The impact of epidermolysis bullosa on quality of life and mental health. [PDF]
Discov Ment HealthMartins Freitas G +3 more
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Nature Reviews Disease Primers, 2020
Epidermolysis bullosa (EB) is an inherited, heterogeneous group of rare genetic dermatoses characterized by mucocutaneous fragility and blister formation, inducible by often minimal trauma. A broad phenotypic spectrum has been described, with potentially severe extracutaneous manifestations, morbidity and mortality.
Bardhan, Ajoy +12 more
semanticscholar +8 more sources
Epidermolysis bullosa (EB) is an inherited, heterogeneous group of rare genetic dermatoses characterized by mucocutaneous fragility and blister formation, inducible by often minimal trauma. A broad phenotypic spectrum has been described, with potentially severe extracutaneous manifestations, morbidity and mortality.
Bardhan, Ajoy +12 more
semanticscholar +8 more sources
British Journal of Dermatology, 2021
The National Health Service (NHS) epidermolysis bullosa (EB) service, established in 2002, offers comprehensive, free care to all patients in England and Wales.
G. Petrof +10 more
semanticscholar +1 more source
The National Health Service (NHS) epidermolysis bullosa (EB) service, established in 2002, offers comprehensive, free care to all patients in England and Wales.
G. Petrof +10 more
semanticscholar +1 more source
Genotype and phenotype correlations in 441 patients with epidermolysis bullosa from China
Journal of the European Academy of Dermatology and Venereology, 2022Epidermolysis bullosa (EB) is a heterogeneous group of rare and incurable genetic blistering disorders.
Fuying Chen +13 more
semanticscholar +1 more source
Journal of the European Academy of Dermatology and Venereology, 2021
Dystrophic epidermolysis bullosa pruriginosa (DEB‐Pr) is a rare subtype of hereditary epidermolysis bullosa, with a poorly understood pathogenesis and no satisfactory treatment.
D. Darbord +11 more
semanticscholar +1 more source
Dystrophic epidermolysis bullosa pruriginosa (DEB‐Pr) is a rare subtype of hereditary epidermolysis bullosa, with a poorly understood pathogenesis and no satisfactory treatment.
D. Darbord +11 more
semanticscholar +1 more source
Epidermolysis bullosa: Pediatric perspectives.
Current pediatric reviews, 2021Epidermolysis bullosa (EB) is a group of rare congenital genetic conditions that result in painful blistering of the skin and mucous membranes which occur with minor trauma or friction.
K. Hon, S. Chu, A. Leung
semanticscholar +1 more source
Pediatric dermatology, 2021
Dystrophic epidermolysis bullosa is a debilitating skin condition, without curative treatment. Previous research has focused on the recessive variant, which is known to cause severe disease.
S. Fulchand +9 more
semanticscholar +1 more source
Dystrophic epidermolysis bullosa is a debilitating skin condition, without curative treatment. Previous research has focused on the recessive variant, which is known to cause severe disease.
S. Fulchand +9 more
semanticscholar +1 more source
Oral Surgery, Oral Medicine, Oral Pathology, 1989
During the last 10 years, there has been considerable progress in the knowledge of epidermolysis bullosa, which has led to recognition of at least 18 different varieties. This review article attempts to classify these varieties and to emphasize the orodental findings in patients with epidermolysis bullosa.
H O, Sedano, R J, Gorlin
openaire +2 more sources
During the last 10 years, there has been considerable progress in the knowledge of epidermolysis bullosa, which has led to recognition of at least 18 different varieties. This review article attempts to classify these varieties and to emphasize the orodental findings in patients with epidermolysis bullosa.
H O, Sedano, R J, Gorlin
openaire +2 more sources
British Journal of Hospital Medicine, 2006
Over the last decade, defining the molecular pathology of the inherited blistering condition, epidermolysis bullosa, has led to more accurate diagnoses, better genetic counselling, the feasibility of DNA-based prenatal diagnosis, and the possibility of newer forms of treatment, including somatic gene therapy.
McGrath, J A, Mellerio, J E
openaire +2 more sources
Over the last decade, defining the molecular pathology of the inherited blistering condition, epidermolysis bullosa, has led to more accurate diagnoses, better genetic counselling, the feasibility of DNA-based prenatal diagnosis, and the possibility of newer forms of treatment, including somatic gene therapy.
McGrath, J A, Mellerio, J E
openaire +2 more sources