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European Journal of Haematology|July 1, 2024
The German sickle cell disease registry reveals a surprising risk of acute splenic sequestration and an increased transfusion requirement in patients with compound heterozygous sickle cell disease HbS/β-thalassaemia and no or low HbA expressionPierre Allard, Laura Tagliaferri, Vivienn Weru, et al.Clinical Immunology (Orlando, Fla.)|December 6, 2016
Newborn screening for severe combined immunodeficiency using a novel and simplified method to measure T-cell excision circles (TREC)Laura Tagliaferri, Joachim B Kunz, Margit Happich, et al.Aging|November 8, 2015
A novel autosomal recessive TERT T1129P mutation in a dyskeratosis congenita family leads to cellular senescence and loss of CD34+ hematopoietic stem cells not reversible by mTOR-inhibitionClemens Stockklausner, Simon Raffel, Julia Klermund, et al.Pediatric Blood & Cancer|December 24, 2019
Sickle cell disease in Germany: Results from a national registryJoachim B Kunz, Stephan Lobitz, Regine Grosse, et al.Orphanet Journal of Rare Diseases|April 16, 2025
COVID- 19 in patients affected by red blood cell disorders, results from the European registry ERN-EuroBloodNetPablo Velasco Puyo, Soteroula Christou, Saveria Campisi, et al.Pageof 2