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Impaired polysaccharide responsiveness without agammaglobulinaemia in three patients with hypomorphic mutations in Bruton Tyrosine Kinase-No detection by newborn screening for primary immunodeficiencies
Krueger, Renate et al. (2019)
Wissenschaftlicher Artikel
Key findings to expedite the diagnosis of hyper-IgE syndromes in infants and young children
Hagl, Beate et al. (2016)
Wissenschaftlicher Artikel
Definition of a critical T cell threshold for prevention of GVHD after HLA non-identical PBPC transplantation in children
Muller, SM et al. (1999)
Wissenschaftlicher Artikel
Frequency of congenital dyserythropoietic anemias in Europe
Heimpel, Hermann et al. (2010)
Wissenschaftlicher Artikel
Familial polycythemia vera with Budd-Chiari syndrome in childhood
Cario, H et al. (2003)
Wissenschaftlicher Artikel
Congenital erythrocytosis and polycythemia vera in childhood and adolescence
Cario, H et al. (2004)
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Reticular dysgenesis: international survey on clinical presentation, transplantation, and outcome
Hoenig, Manfred et al. (2017)
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Angiotensin I converting enzyme and angiotensinogen gene polymorphisms related to 24-h blood pressure in paediatric type I diabetes mellitus
Pavlovic, M et al. (1999)
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Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis
Cario, H et al. (2005)
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Breaking chemoresistance and radioresistance with [Bi-213]anti-CD45 antibodies in leukemia cells
Friesen, Claudia et al. (2007)
Wissenschaftlicher Artikel