32 results on '"Lämmle B"'
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2. Neonatal exchange transfusion: hereditary thrombotic thrombocytopenic purpura (hTTP) should be in the differential diagnosis
3. Conclusion from 50 years of reports on prekallikrein or high-molecular-weight kininogen deficiency
4. Komplexe Gerinnungsstörungen
5. Pregnancy Outcomes in Hereditary Thrombotic Thrombocytopenic Purpura – Room for (Further) Improvement.
6. Detection and Differential Diagnosis of Prekallikrein Deficiency: Genetic Study of New Families and Systematic Review of the Literature
7. 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?
8. Eleven Relapses in a Cohort of 78 Patients with Immune Thrombotic Thrombocytopenic Purpura (iTTP): Data from the German TTP-Registry
9. T-18-04: The Von Willebrand factor multimer ratio and inflammatory markers in autoimmune thrombotic thrombocytopenic purpura.
10. T-17-01: Conclusion from 50 years of reports on prekallikrein or high-molecular-weight kininogen deficiency.
11. T-03-04: Neonatal exchange transfusion: hereditary thrombotic thrombocytopenic purpura (hTTP) should be in the differential diagnosis.
12. Late onset and pregnancy-induced congenital thrombotic thrombocytopenic purpura
13. Bilateral periorbital ecchymoses
14. Pearls, guidelines & more
15. Qualitative platelet defect and thrombohaemorrhagic complications in a patient with polycythaemia vera. Case 10
16. Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry
17. Hämorrhagische und thromboembolische Störungen
18. Acquired von Willebrand syndrome in myeloproliferative disorder
19. Schistocytic anaemia, severe thrombocytopenia, and renal dysfunction: thrombotic microangiopathy due to severe acquired ADAMTS-13 deficiency
20. Therapie der akuten tiefen Beinvenenthrombose mit niedermolekularen Heparinen
21. Hereditary thrombotic thrombo-cytopenic purpura and the hereditary TTP registry.
22. Late onset and pregnancy-induced congenital thrombotic thrombocytopenic purpura
23. Bilateral periorbital ecchymoses
24. Protein S und venöse Thrombophilie
25. Therapie der akuten tiefen Beinvenenthrombose mit niedermolekularen Heparinen
26. Protein S und venöse Thrombophilie
27. 100 Years of Thrombotic Thrombocytopenic Purpura: A Story of Death and Life.
28. Clinical Problem Solving and Using New Paths in the Laboratory: Learning from Case Studies.
29. May-Thurner syndrome: missed diagnosis and missed early treatment?
30. Bilateral periorbital ecchymoses. An often missed sign of amyloid purpura.
31. Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry.
32. Acquired von Willebrand syndrome in a myeloproliferative disorder. Case 6.
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