Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Marieke Bolling"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)
Abstract Background Epidermolysis bullosa is a rare, often severe, genetic disorder characterized by fragility of the skin and mucous membranes. Despite the important role of parents during wound care, an essential factor in adapting to this disease,
Externí odkaz:
https://doaj.org/article/c4a05db33c8d43b5a563cfafc49d9048
The relationship between quality of life and coping strategies of children with EB and their parents
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Background Epidermolysis bullosa (EB) is a group of rare genetic skin disorders that primarily manifest as blisters and erosions following mild mechanical trauma. Despite the crucial role of the parents of children with EB in managing the di
Externí odkaz:
https://doaj.org/article/d23175e5999c49f59720646b4334e69d
Autor:
Marjorie Pion, Esther Bernaldo-de-Quirós, Rebeca Kennedy-Batalla, Marta Martínez-Bonet, Antonio Torrelo, Begoña Carazo-Gallego, Angela Hernández-Martín, Elvira Cañedo, Rafael Correa-Rocha, Lucero Noguera-Morel, Marieke Bolling, Rogelio González-Sarmiento, Angel Vera
Publikováno v:
New England Journal of Medicine. 381:2176-2178
T-Helper 17 Cells in Genetic Dermatitis An infant with SAM-like syndrome (severe dermatitis, allergies, and metabolic wasting) was found to have a substantial increase in the number of T-helper 17 ...
Publikováno v:
Nederlands Tijdschrift voor Dermatologie en Venereologie, 27(6), 322-325. DCHG Partners in Mediscne Communicatie
University of Groningen
University of Groningen
A 27-year-old male with recessive dystrophic epidermolysis bullosa, severe generalized (RDEB-SG), presented with a tumor on the left lateral malleolus that had been present for six months. Histopathologic examination showed a moderate to well differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4e4fecd0e7480e97215dd4745b0a462e
https://research.rug.nl/en/publications/3956c3d1-8225-4c13-9a30-88e88e4ef13a
https://research.rug.nl/en/publications/3956c3d1-8225-4c13-9a30-88e88e4ef13a