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25 results on '"Hoffmann, Marianne"'

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1. DAHEAN: A Danish nationwide study ensuring quality assurance through real-world data for suspected hereditary anemia patients

2. A Rare Case of <italic>De Novo</italic> Beta-Thalassemia Diagnosed by Whole-Genome Sequencing in an Ethnically Danish Newborn.

3. Dabigatran etexilate for the treatment of acute venous thromboembolism in children (DIVERSITY): a randomised, controlled, open-label, phase 2b/3, non-inferiority trial

6. Addition of plasma exchange to red cell exchange improves outcomes of fat embolism syndrome in sickle cell disease

7. A survey on thromboprophylaxis and coagulation assessment in children and young adults with acute lymphoblastic leukaemia ( ALL ) in the Nordic and Baltic countries: Different practices of assessment and management

8. Intracranial haemorrhage in children and adolescents with severe haemophilia A or B – the impact of prophylactic treatment

12. Dabigatran etexilate for the treatment of acute venous thromboembolism in children (DIVERSITY): a randomised, controlled, open-label, phase 2b/3, non-inferiority trial

13. Additional file 1 of Interprofessional versus monoprofessional case-based learning in childhood cancer and the effect on healthcare professionals’ knowledge and attitudes: study protocol for a randomised trial

14. Twelve tips for postgraduate interprofessional case-based learning.

16. Flow cytometric analysis of cerebrospinal fluid improves detection of leukaemic blasts in infants with acute lymphoblastic leukaemia.

18. Clinical impact of leukemic blast heterogeneity at diagnosis in cytogenetic intermediate-risk acute myeloid leukemia

19. The Prognostic Impact of Blast Cell Immunophenotyping in Intermediate Risk AML Patients at Diagnosis.

20. Interaction of Actin and Myosin in the Absence and Presence of ATP

23. Mary Kelly 'A Father and Child'.

24. [Challenges and advances in paediatric arterial ischaemic stroke].

25. Multiplex reverse transcription polymerase chain reaction screening in acute myeloid leukemia detects cytogenetically unrevealed abnormalities of prognostic significance.

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