39 results on '"Fujimura, Yoshihiro"'
Search Results
2. Patent ductus arteriosus generates neonatal hemolytic jaundice with thrombocytopenia in Upshaw-Schulman syndrome
3. Blood group antigen A on von Willebrand factor is more protective against ADAMTS13 cleavage than antigens B and H
4. Recombinant ADAMTS-13: first-in-human pharmacokinetics and safety in congenital thrombotic thrombocytopenic purpura
5. Mutations and Common Polymorphisms in ADAMTS13 Gene Responsible for von Willebrand Factor-Cleaving Protease Activity
6. Familial C3 glomerulonephritis associated with mutations in the gene for complement factor B
7. Two Mechanistic Pathways for Thienopyridine-Associated Thrombotic Thrombocytopenic Purpura: A Report From the SERF-TTP Research Group and the RADAR Project
8. Successful Treatment of Primitive Neuroectodermal Tumor-associated Microangiopathy with Multiple Bone Metastases
9. Novel compound heterozygote mutations (H234Q/R1206X) of the ADAMTS13 gene in an adult patient with Upshaw–Schulman syndrome showing predominant episodes of repeated acute renal failure
10. Plasma ADAMTS13 activity may predict early adverse events in living donor liver transplantation: Observations in 3 cases
11. Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome
12. Primary structure of two-chain botrocetin, a von Willebrand factor modulatorpurified from the venom of Bothrops jararaca
13. Mural thrombus generation in type 2A and 2B von Willebrand disease under flow conditions
14. UV light-emitting diode (UV-LED) at 265 nm as a potential light source for disinfecting human platelet concentrates.
15. ABO Blood Group Antigens on Human Plasma von Willebrand Factor After ABO-Mismatched Bone Marrow Transplantation
16. The cDNA cloning of human placental ecto-ATP diphosphohydrolases I and II
17. A note on the carrier detection of hemophilia a
18. von Willebrand Factor-Rich Platelet Thrombi in the Liver Cause Sinusoidal Obstruction Syndrome following Oxaliplatin-Based Chemotherapy.
19. A Novel Quantitative Hemolytic Assay Coupled with Restriction Fragment Length Polymorphisms Analysis Enabled Early Diagnosis of Atypical Hemolytic Uremic Syndrome and Identified Unique Predisposing Mutations in Japan.
20. STEC:O111-HUS complicated by acute encephalopathy in a young girl was successfully treated with a set of hemodiafiltration, steroid pulse, and soluble thrombomodulin under plasma exchange.
21. A Unique Case Involving a Female Patient with Upshaw-Schulman Syndrome: Low Titers of Antibodies against ADAMTS13 prior to Pregnancy Disappeared after Successful Delivery.
22. Candidate gene analysis using genomic quantitative PCR: identification of ADAMTS13 large deletions in two patients with Upshaw- Schulman syndrome.
23. Long term follow up of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) on hemodialysis for 19 years: a case report.
24. Ratio of von Willebrand Factor Propeptide to ADAMTS13 Is Associated With Severity of Sepsis.
25. Acquired Idiopathic ADAMTS13 Activity Deficient Thrombotic Thrombocytopenic Purpura in a Population from Japan.
26. Determination of ADAMTS13 and Its Clinical Significance for ADAMTS13 Supplementation Therapy to Improve the Survival of Patients with Decompensated Liver Cirrhosis.
27. Von Willebrand factor-cleaving protease activity in thrombotic microangiopathy after living donor liver transplantation: A case report.
28. Successful treatment of a young infant who developed high-titer inhibitors against VWF-cleaving protease (ADAMTS-13): Important discrimination from Upshaw-Schulman syndrome.
29. Enhanced low shear stress induced platelet aggregation by Shiga-like toxin 1 purified from Escherichia coli O157.
30. Spontaneous platelet aggregation in type IIB tampa von willebrand disease is inhibited by the 52/48-kDa fragment of normal von willebrand factor, which contains the GPIb binding domain.
31. Purification and amino acid sequence of halystase from snake venom of Agkistrodon halys blomhoffii, a serine protease that cleaves specifically fibrinogen and kininogen.
32. Long term follow up of congenital thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) on hemodialysis for 19 years: a case report.
33. Structural Elements Influencing von Willebrand Factor (vWF) Binding Affinity for Platelet Glycoprotein Ib Within a Dispase-Digested vWF Fragment
34. High Shear Stress Can Initiate Both Platelet Aggregation and Shedding of Procoagulant Containing Microparticles
35. Role and Initiation Mechanism of the Interaction of Glycoprotein Ib With Surface-Immobilized von Willebrand Factor in a Solid-Phase Platelet Cohesion Process
36. Human plasma alpha 2-macroglobulin and von Willebrand factor possess covalently linked ABO(H) blood group antigens in subjects with corresponding ABO phenotype
37. The von Willebrand Factor Domain–Mediating Botrocetin-Induced Binding to Glycoprotein IB Lies Between Val449 and Lys728
38. Author's reply.
39. Ticlopidine- and clopidogrel-associated thrombotic thrombocytopenic purpura (TTP): review of clinical, laboratory, epidemiological, and pharmacovigilance findings (1989–2008).
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