Found: 4
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Neonatal antiphospholipid syndrome associated with heterozygous methylentetrahydrofolate reductase C677T and prothrombin G20210A gene mutations.
- Published in:
- Rheumatology, 2007, v. 46, n. 4, p. 720
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- Article
First prospective report on immune tolerance in poor risk haemophilia A inhibitor patients with a single factor VIII/von Willebrand factor concentrate in an observational immune tolerance induction study.
- Published in:
- Haemophilia, 2016, v. 22, n. 1, p. 87, doi. 10.1111/hae.12774
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- Publication type:
- Article
Spectrum of F8 gene mutations in haemophilia A patients from Slovenia.
- Published in:
- Haemophilia, 2012, v. 18, n. 6, p. e420, doi. 10.1111/hae.12003
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- Publication type:
- Article
Diagnostic accuracy of procalcitonin and interleukin-6 values for predicting bacteremia and clinical sepsis in febrile neutropenic children with cancer.
- Published in:
- European Journal of Clinical Microbiology & Infectious Diseases, 2006, v. 25, n. 6, p. 413, doi. 10.1007/s10096-006-0143-x
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- Article