169 results on '"Ikejiri, Makoto"'
Search Results
2. Characteristic genetic spectrum of primary ciliary dyskinesia in Japanese patients and global ethnic heterogeneity: population-based genomic variation database analysis
3. Dual Inhibition of CYP3A4 by Voriconazole and Clarithromycin Influences Tacrolimus Pharmacokinetics: Case Series Study
4. Analysis of the diagnosis of Japanese patients with primary ciliary dyskinesia using a conditional reprogramming culture
5. Precision cancer genome testing needs proficiency testing involving all stakeholders
6. Succinate dehydrogenase B-deficient renal cell carcinoma with a germline variant in a Japanese patient: a case report
7. Two Pediatric Cases of Primary Ciliary Dyskinesia Caused by Loss‐of‐Function Variants in Oral‐Facial‐Digital Syndrome Gene, OFD1.
8. Primary cytomegalovirus infection during pregnancy and congenital infection: a population-based, mother–child, prospective cohort study
9. MPL exon 10 mutations other than canonical MPL W515L/K mutations identified by in-house MPL exon 10 direct sequencing in essential thrombocythemia
10. Cytomegalovirus DNA Loads in Organs of Congenitally Infected Fetus.
11. A pediatric case of productive cough caused by novel variants in DNAH9
12. Usefulness of the APTT waveform for the diagnosis of DIC and prediction of the outcome or bleeding risk
13. A substitution in the pre-S1 promoter region is associated with the viral regulation of hepatitis B virus
14. High prevalence of congenital thrombophilia in patients with pregnancy-related or idiopathic venous thromboembolism/pulmonary embolism
15. Elevated plasma levels of soluble platelet glycoprotein VI (GPVI) in patients with thrombotic microangiopathy
16. Major bleeding in a patient with warfarin-hypersensitive and factor IX propeptide variant, p.Ala37Thr, who was treated with a direct oral anti-Xa inhibitor
17. Analysis of Otologic Features of Patients With Primary Ciliary Dyskinesia
18. Transient Decrease in Incidence Rate of Maternal Primary Cytomegalovirus Infection during the COVID-19 Pandemic in Japan.
19. Comparison of three different anti-Xa assays in major orthopedic surgery patients treated with fondaparinux
20. Revision of Cytomegalovirus Immunoglobulin M Antibody Titer Cutoff in a Maternal Antibody Screening Program in Japan: A Cohort Comparison Involving a Total of 32,000 Pregnant Women.
21. Psychological characteristics of Japanese patients and their family members receiving genetic counseling: A single‐institute exploratory study.
22. High frequency of decreased antithrombin level in pregnant women with thrombosis
23. Analysis of patients with atypical hemolytic uremic syndrome treated at the Mie University Hospital: concentration of C3 p.I1157T mutation
24. Clinical features and underlying causes of cerebral venous thrombosis in Japanese patients
25. Analysis three abnormal Protein S genes in a patient with pulmonary embolism
26. MO16-3 Clinical relevance of comprehensive genome profiling using real-world data in colorectal cancer
27. Evaluation of bleeding and anticoagulation markers by edoxaban and low‐dose cyclosporine: A case series study.
28. Presence of antiphospholipid antibody is a risk factor in thrombotic events in patients with antiphospholipid syndrome or relevant diseases
29. Frequent association of thrombophilia in cerebral venous sinus thrombosis
30. The association of protein S Tokushima-K196E with a risk of deep vein thrombosis
31. Des-γ-carboxy prothrombin ratio measured by P-11 and P-16 antibodies is a novel biomarker for hepatocellular carcinoma
32. The Effectiveness of Measuring for Fragmented Red Cells Using an Automated Hematology Analyzer in Patients With Thrombotic Microangiopathy
33. Primary ciliary dyskinesia with CCDC39 variants displaying specific ciliary ultrastructure and movement concordant with the genotype: A case report
34. Acquisition of JAK2 V617F to CALR‐mutated clones accelerates disease progression and might enhance growth capacity.
35. P52-5 Effort of Cancer Genome Center Hospital in Rural National University
36. P1061: CLINICAL FEATURES OF PHILADELPHIA‐NEGATIVE MPN DEVELOPED IN ADOLESCENTS AND YOUNG ADULTS IN JAPAN.
37. A novel protein S gene mutation combined with protein S Tokushima mutation in a patient with superior sagittal sinus thrombosis
38. Multifaceted analysis of Japanese cases of primary ciliary dyskinesia: Value of immunofluorescence for ciliary protein detection in patients with DNAH5 and DNAH11 mutations
39. RHOF PROMOTES MURINE MARGINAL ZONE B CELL DEVELOPMENT
40. Copy number variation in DRC1 is the major cause of primary ciliary dyskinesia in the Japanese population.
41. Clinical Manifestation of Patients With Atypical Hemolytic Uremic Syndrome With the C3 p.I1157T Variation in the Kinki Region of Japan.
42. Routine measurements of factor VIII activity and inhibitor titer in the presence of emicizumab utilizing anti‐idiotype monoclonal antibodies: comment
43. Frequent association of thrombophilia in cerebral venous sinus thrombosis
44. An Evaluation of Hemostatic Abnormalities in Patients With Hemophilia According to the Activated Partial Thromboplastin Time Waveform.
45. An Evaluation of the Activated Partial Thromboplastin Time Waveform.
46. Analysis of Otologic Features of Patients With Primary Ciliary Dyskinesia.
47. Hypofibrinogenemia and the α-Fibrinogen Thr312Ala Polymorphism may be Risk Factors for Early Pregnancy Loss.
48. A case of dichorionic diamniotic twin pregnancy suspected with primary cytomegalovirus infection by maternal cytomegalovirus serological screening
49. Development of cutaneous squamous cell carcinoma during pembrolizumab therapy.
50. Establishment of Mouse Model of MYH9 Disorders: Heterozygous R702C Mutation Provokes Macrothrombocytopenia with Leukocyte Inclusion Bodies, Renal Glomerulosclerosis and Hearing Disability.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.