Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Selma Kofoed Bendtsen"'
Autor:
Andreas Glenthøj, Andreas Ørslev Rasmussen, Selma Kofoed Bendtsen, Henrik Hasle, Marianne Hoffmann, Klaus Rieneck, Morten Hanefeld Dziegiel, Lene Dissing Sjö, Henrik Frederiksen, Dennis Lund Hansen, Daniel El Fassi, Mathias Rathe, Peter-Diedrich Matthias Jensen, Anne Winther-Larsen, Christian Nielsen, Marianne Olsen, Nina Toft, Mads Okkels Birk Lorenzen, Lise Heilmann Jensen, Sif Gudbrandsdottir, Jens Helby, Maria Rossing, Richard van Wijk, Jesper Petersen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background Hereditary anemias are a group of genetic diseases prevalent worldwide and pose a significant health burden on patients and societies. The clinical phenotype of hereditary anemias varies from compensated hemolysis to life-threaten
Externí odkaz:
https://doaj.org/article/571fe371a8f54ba6b50bfb5757c53faf
Autor:
Niels Vejlstrup, Pierre Fenaux, Jesper Petersen, Eduard J van Beers, Andreas Glenthøj, Kevin H M Kuo, Richard van Wijk, Minke A E Rab, Evelyn Groot, Nina Toft, Selma Kofoed Bendtsen, Jens Helby, Fatiha Chermat
Publikováno v:
BMJ Open, Vol 14, Iss 7 (2024)
Introduction Membranopathies encompass haemolytic disorders arising from genetic variants in erythrocyte membrane proteins, including hereditary spherocytosis and stomatocytosis. Congenital dyserythropoietic anaemia type II (CDA II) is associated wit
Externí odkaz:
https://doaj.org/article/6958cd02f6274f47ad7b9e2b612e7a5c