14 results on '"Alesci S"'
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2. Age-related evaluation of clinical manifestation and treatment of von Willebrand disease evaluated in an open-label, prospective, non-interventional study (wilate®-set): PO-MO-236
3. Incidence of inhibitors against FVIII or FIX in PTPs after switching factor concentrate during the presence of immunological danger signals: PO-WE-117
4. Successful treatment of an injury bleeding on a patient suffering from mild von Willebrandʼs disease and predisposition to allergic diseases, with recombinant factor VIIA
5. Association between phenotype and genotype in carriers of haemophilia A
6. Latest interim results from a German prospective post-marketing surveillance of treatment of von Willebrand disease with a new generation VWF/FVIII concentrate: 35P33
7. Retrospective analysis of the clinical efficacy and safety of Humate® P in patients treated with Humate® P for more than 5 years: 35P27
8. Correlation between clinical data, laboratory results and adverse reactions after administration of desmopressin (DDAVP): 35P26
9. Efficacy and safety of KOGENATE® Bayer in patients with haemophilia A during surgical procedures: 08P27
10. Age-dependent increase of FVIII: C in mild haemophilia A
11. Comorbidities and bleeding pattern in elderly haemophilia A patients
12. Association between phenotype and genotype in carriers of haemophilia A
13. Successful treatment of an injury bleeding on a patient suffering from mild von Willebrand’s disease and predisposition to allergic diseases, with recombinant factor VIIA
14. Age‐dependent increase of FVIII:C in mild haemophilia A
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