38 results on '"Lämmle B"'
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2. More severe ADAMTS13 Deficiency in Homozygous versus Compound Heterozygous Carriers of the ADAMTS13 c.4143_4144dupA Mutation in Congenital Thrombotic Thrombocytopenic Purpura (cTTP): Impact on Disease Onset?
3. Eleven Relapses in a Cohort of 78 Patients with Immune Thrombotic Thrombocytopenic Purpura (iTTP): Data from the German TTP-Registry
4. Derivation and validation of a novel bleeding risk score for elderly patients with venous thromboembolism on extended anticoagulation
5. Prevalence of Depression in patients with diagnosis of thrombotic thrombocytopenic purpura (TTP)
6. Prevalence of depression in patients with diagnosis of thrombotic thrombocytopenic purpura (TTP)
7. Late onset and pregnancy-induced congenital thrombotic thrombocytopenic purpura
8. Bilateral periorbital ecchymoses
9. Pearls, guidelines & more
10. Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry
11. Qualitative platelet defect and thrombohaemorrhagic complications in a patient with polycythaemia vera
12. Hämorrhagische und thromboembolische Störungen
13. Acquired von Willebrand syndrome in myeloproliferative disorder
14. Schistocytic anaemia, severe thrombocytopenia, and renal dysfunction: thrombotic microangiopathy due to severe acquired ADAMTS-13 deficiency
15. High Molecular Weight Kininogen Is Cleaved by FXIa at Three Sites: Arg409-Arg410, Lys502-Thr503 and Lys325-Lys326
16. Reevaluation of the Incidence of Thromboembolic Complications in Congenital Factor XII Deficiency
17. Is Plasminogen Deficiency a Thrombotic Risk Factor ? – A Study on 23 Thrombophilic Patients and their Family Members
18. SimpliRED D-dimer Assay: Comparability of Capillary and Citrated Venous Whole Blood, Between-assay Variability, and Performance of the Test for Exclusion of Deep Vein Thrombosis in Symptomatic Outpatients
19. Therapie der akuten tiefen Beinvenenthrombose mit niedermolekularen Heparinen
20. Plasminogen Deficiency: An Additional Risk Factor for Thrombosis in a Family with Factor V R506Q Mutation?
21. Functional Characterization of a Variant Prekallikrein (PK Zürich)
22. Rebuttal to the Letter of F. Rodeghiero et al. -Thrombosis in Subjects with Homozygous and Heterozygous Factor XII Deficiency
23. Major Coagulation Disorders when using Aprotinin - Observations on a Case
24. Rebuttal to the Letter to the Editor by W. P. M. Houdijk
25. Decreased Free Protein S Levels in Polycythemia Vera
26. Prekallikrein Activator - Reply
27. Protein S und venöse Thrombophilie
28. The Contact Phase of Blood Coagulation in Diabetes Mellitus and in Patients with Vasculopathy
29. Plasmin Inhibitors and Fibrinogen Breakdown During the Initial Phase of Thrombolytic Treatment - The Problem of the α2-Antiplasmin Determination
30. Fifteen Coagulation and Fibrinolysis Parameters in Diabetes Mellitus and in Patients with Vasculopathy
31. In Vitro Effects of the Acylated StreptokinasePlasminogen Activator Complex BRL 33 575 Incubated with Normal Human Plasma
32. Cold Promoted Activation and Factor XII, Prekallikrein and C1-Inhibitor
33. Factor XII, Plasma Prekallikrein, α2-Macroglobulin and C1-Inhibitor Levels in Renal Allograft Recipients During Immunosuppression with Cyclosporin A – Sequential Measurements over Four Months in 17 Patients
34. Haemorrhagic Shock Nine Days after Extracorporeal Shock Wave Lithotripsy in a Patient with Haemophilia B
35. Platelet Aggregation, β-Thromboglobulin and Platelet Factor 4 in Diabetes Mellitus and in Patients with Vasculopathy
36. 1,25 (OH)2Vitamin D3in Osteoporosis - A Pilot Study
37. Monitoring of Oral Anticoagulation by an Amidolytic Factor X Assay
38. Heparin Cofactor II: Purification and Antibody Production
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