Jenny Klintman
0000-0002-9544-5058
Lund University
16 papers found
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Bone mineral density in haemophilia – a multicentre study evaluating the impact of different replacement regimens
Clinical characterization and identification of rare genetic variants in atypical hemolytic uremic syndrome: a Swedish retrospective observational study
The prospective Hemophilia Inhibitor PUP Study reveals distinct antibody signatures prior to FVIII inhibitor development
SAMHD1 Limits the Efficacy of Forodesine in Leukemia by Protecting Cells against the Cytotoxicity of dGTP
First-line therapy in chronic lymphocytic leukemia: a Swedish nation-wide real-world study on 1053 consecutive patients treated between 2007 and 2013
Clinical-grade validation of whole genome sequencing reveals robust detection of low-frequency variants and copy number alterations in CLL
Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia
Indications of underdiagnosis of atypical haemolytic uraemic syndrome in a cohort referred to the Coagulation Unit in Malmo, Sweden, for analysis of ADAMTS13 2007-2012
At the Cross Section of Thrombotic Microangiopathy and Atypical Hemolytic Uremic Syndrome: A Narrative Review of Differential Diagnostics and a Problematization of Nomenclature
Epidemiological aspects of inhibitor development in hemophilia and strategies of management
Long-term anti-FVIII antibody response in Bethesda-negative haemophilia A patients receiving continuous replacement therapy
Antibody formation and specificity in Bethesda-negative brother pairs with haemophilia A
Combination of FVIII and by-passing agent potentiates in vitro thrombin production in haemophilia A inhibitor plasma
Thrombin generation in vitro in the presence of by-passing agents in siblings with severe haemophilia A
Quiescence of hematopoietic stem cells and maintenance of the stem cell pool is not dependent on TGF-β signaling in vivo
Haematopoietic stem cells retain long-term repopulating activity and multipotency in the absence of stem-cell leukaemia SCL/tal-1 gene
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