1,279 results on '"Scharrer I"'
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2. Influence of hypothyroidism on blood coagulation and the acquired von Willebrand syndrome
3. Thrombotisch-thrombozytopenische Purpura
4. The Importance of Pre-Analytic Conditions on the Determination of VWF Parameters
5. Investigation of the Tendency to Bleeding in Patients with low Activity of Plasminogen Activator Inhibitor-1 (PAI-1)
6. The Role of VWF:Ag II in Patients with Acquired von Willebrand Disease
7. Bleeding Tendency of Carriers of Hemophilia A — Dependent on the Age of the Carriers?
8. HLA Profile in Acquired Hemophilia
9. Major Orthopedic Reconstructions in an Inhibitor Patient — A Case Report
10. Total Hip Replacement in Patients with Severe Bleeding Disorders A 30 Years Single Center Experience
11. Perioperative Substitutionstherapie
12. Tissue Factor Pathway Inhibitor (TFPI): Nachweis und Bestimmung in der Synovialflüssigkeit großer Gelenke
13. Pathophysiologie der hämorrhagischen Diathesen
14. Psychosoziale Auswirkungen der hämophilen Arthropathie
15. One Year TTP Diagnosis in the Central Laboratory of the University of Mainz
16. Mutation Analysis of the C1 Inhibitor Gene
17. Case report: 58-Year-Old Hemophilia A Patient with High-Titer Inhibitor Development and Introduction of a Multicenter PTP-Inhibitor Study
18. Identification of Inhibitor Epitopes in Acquired Hemophilia by Phage Display
19. Inhibitors in PTP’S: A Retrospective Study in Germany
20. Testing Factor VIII Activity by Using the Chromogenic Assay in Carriers of Hemophilia A
21. Clinical Manifestations of Patients with Dysfibrinogenemia
22. Malignancy is not Associated with Decreased ADAMTS-13 Activity in Patients with Brain Tumors
23. Bleeding Symptoms in Carriers of Hemophilia A — Association to the Factor VIII Gene Mutation?
24. Clinical Manifestations of Patients with Highly Elevated Anticardiolipin Antibodies
25. Von-Willebrand Factor Cleaving Protease (ADAMTS-13) Activity in Various Thrombotic, Hemolytic and Autoimmune Disorders
26. A Retrospective Study on the Development of Inhibitors after Continuous Infusion of Factor VIII
27. Cardiac and cerebral Manifestations of the Antiphospholipid Syndrome
28. Dysfibrinogenemia following after Snake Bite
29. Is there a Correlation between vWF-cleaving Protease-Activity, vWF:Ag, Clinical Course and Number of Relapses in 15 Patients with TTP?
30. Early and rapid Diagnosis of acute TTP by Measuring Activity of von-Willebrand Factor cleaving Metalloprotease (ADAMTS13): A Case Report
31. Factor V Inhibitor and Anti-Phospholipid Antibodies after Treatment with Ciprofloxacin
32. Role of a 23 bp Insertion in Exon 3 of the Endothelial Cell Protein C Receptor Gene in Venous Thrombophilia
33. Do Statins Increase the Homocysteine Level?
34. Thrombophilic Risk Parameters in Juvenile »Idiopathic« Stroke Patients
35. Inquiry into the Significance of Constantly Raised FVIII Values as a Factor in Thrombophilia
36. Johann Lukas Schoenlein Award 2000
37. Untersuchungen zur Multimerenstruktur in Präparaten zur Therapie des von Willebrand-Syndroms
38. Induktion eines von Willebrand-Syndroms Typ I unter Valproat-Therapie
39. Untersuchungen zur Häufigkeit der Hemmkörperbildung nach Behandlung mit monoklonalen Antikörpern gereinigtem Faktor VIII:C-Konzentrat
40. Nicht-infektiöse Nebenwirkungen gerinnungsaktiver Plasmapräparate
41. Diskussion
42. Anti-HCV und Hepatitis bei Patienten mit Blutgerinnungsstörungen
43. Leberzirrhose und Gerinnungsstörungen
44. Long-Term Results After Total Knee and Total Hip Replacement in Hemophilic Arthropathy
45. Effect of Vitamin Supplementation in Venous Thrombosis Patients with Hyperhomocysteinemia
46. Adsorptionsplasmapherese — eine neue Therapiemöglichkeit für Faktor VIII-Inhibitoren
47. Erfahrungen mit einem monoklonal gereinigten Faktor VIII-Präparat bei 27 Patienten über einen Zeitraum bis zu 2 Jahren
48. Erste klinische Erfahrungen mit rekombinantem Faktor VIII
49. Rekombinante Faktor VIII-Konzentrate
50. Vorläufige Ergebnisse der Anti-HCV-Testung von Patienten mit Blutgerinnungsstörungen
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