110 results on '"Lämmle B"'
Search Results
2. OC 42.3 Immune-Mediated TTP Patients in Remission with Recovered ADAMTS13 Activity but an Open ADAMTS13 Conformation are at Risk for Earlier ADAMTS13 Relapse
3. The Von Willebrand factor multimer ratio and inflammatory markers in autoimmune thrombotic thrombocytopenic purpura
4. Neonatal exchange transfusion: hereditary thrombotic thrombocytopenic purpura (hTTP) should be in the differential diagnosis
5. Conclusion from 50 years of reports on prekallikrein or high-molecular-weight kininogen deficiency
6. P1528: GENETIC AND PHENOTYPIC CHARACTERIZATION OF HEREDITARY SPHEROCYTOSIS AND RELATED DISORDERS – DESCRIPTION OF 9 NEW GENETIC VARIANTS
7. Komplexe Gerinnungsstörungen
8. ADAMTS13 activity, von Willebrand factor, factor VIII and D-dimers in COVID-19 inpatients
9. Apoptosis In Sepsis And Multiple Organ Dysfunction Syndrome
10. Founder Effect of the Factor-IX-Propeptide-Val-10 Variant Is Responsible for Most Marcumar-lnduced Severe Haemophilia B Cases During Oral Anticoagulant Therapy — Consequences for Monitoring
11. Bedeutung der von-Willebrand-Faktor-spaltenden Protease in Diagnostik und klinischem Verlauf bei Patienten mit thrombotisch-thrombozytopenischer Purpura (TTP) und hämolytisch-urämischem Syndrom (HUS)
12. Detection and Differential Diagnosis of Prekallikrein Deficiency: Genetic Study of New Families and Systematic Review of the Literature
13. 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?
14. Eleven Relapses in a Cohort of 78 Patients with Immune Thrombotic Thrombocytopenic Purpura (iTTP): Data from the German TTP-Registry
15. Venöse Thromboembolie in Schwangerschaft und Puerperium: Pathophysiologie, Therapie, Prophylaxe
16. Messung des Thrombin-Antithrombin-III-Komplexes ist kein brauchbarer Screening-Test zur Diagnose des Protein C-und Protein S-Mangels
17. Derivation and validation of a novel bleeding risk score for elderly patients with venous thromboembolism on extended anticoagulation
18. Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies
19. Association between thyroid dysfunction and venous thromboembolism in the elderly: a prospective cohort study
20. High prevalence of hereditary thrombotic thrombocytopenic purpura in central Norway: from clinical observation to evidence
21. Prevalence of Depression in patients with diagnosis of thrombotic thrombocytopenic purpura (TTP)
22. Prevalence of depression in patients with diagnosis of thrombotic thrombocytopenic purpura (TTP)
23. Impaired DNase1‐mediated degradation of neutrophil extracellular traps is associated with acute thrombotic microangiopathies
24. In vitro rescue of FGA deletion by lentiviral transduction of an afibrinogenemic patient's hepatocytes
25. Late onset and pregnancy-induced congenital thrombotic thrombocytopenic purpura
26. Bilateral periorbital ecchymoses
27. Pearls, guidelines & more
28. Prospective, multicenter validation of prediction scores for major bleeding in elderly patients with venous thromboembolism
29. Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry
30. Prospective comparison of clinical prognostic scores in elder patients with a pulmonary embolism
31. Low-dose recombinant factor VIIa for massive bleeding: A single centre observational cohort study with 73 patients
32. Screening for lupus anticoagulant: improving the performance of the lupus-sensitive PTT-LA
33. Das Problem der «Ghost and Guest Authors»
34. Das Problem der «Ghost and Guest Authors»
35. Variability of anti‐PF4/heparin antibody results obtained by the rapid testing system ID‐H/PF4‐PaGIA
36. Variability of anti‐PF4/heparin antibody results obtained by the rapid testing system ID‐H/PF4‐PaGIA: reply to a rebuttal
37. Venous thrombosis after Caesarean section in a young woman with homozygous APC resistance and type I protein S deficiency
38. Low molecular weight heparin-induced thrombocytopenia and skin necrosis distant from injection sites
39. Hématologie: Rivaroxaban, la nouvelle étoile dans le ciel de lanticoagulation orale?
40. Hämatologie: Rivaroxaban, der neue Stern am Himmel der oralen Antikoagulation?
41. Second international collaborative study evaluating performance characteristics of methods measuring the von Willebrand factor cleaving protease (ADAMTS‐13)
42. ADAMTS‐13, von Willebrand factor and related parameters in severe sepsis and septic shock
43. DOSING LEPIRUDIN IN PATIENTS WITH HEPARIN-INDUCED THROMBOCYTOPENIA AND VARIOUS DEGREES OF RENAL FUNCTION IMPAIRMENT
44. Hyperbilirubinemia interferes with ADAMTS‐13 activity measurement by FRETS‐VWF73 assay: diagnostic relevance in patients suffering from acute thrombotic microangiopathies
45. A new tool to further explore the role of ADAMTS‐13 in health and disease
46. Measurement of ADAMTS‐13 activity in plasma by the FRETS‐VWF73 assay: comparison with other assay methods
47. Treatment of thrombotic thrombocytopenic purpura
48. Diagnostic Criteria for Hematopoietic Stem Cell Transplantation-Associated Microangiopathy (TAM): Results of a Consensus Process by an International Working Group.
49. Thrombotic thrombocytopenic purpura
50. The incidence of thrombotic thrombocytopenic purpura‐hemolytic uremic syndrome: all patients, idiopathic patients, and patients with severe ADAMTS‐13 deficiency
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