76 results on '"Ikejiri, Makoto"'
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2. MO16-3 Clinical relevance of comprehensive genome profiling using real-world data in colorectal cancer
3. Analysis of clinical features of Japanese patients with primary ciliary dyskinesia
4. P1061: CLINICAL FEATURES OF PHILADELPHIA-NEGATIVE MPN DEVELOPED IN ADOLESCENTS AND YOUNG ADULTS IN JAPAN
5. Transient Decrease in Incidence Rate of Maternal Primary Cytomegalovirus Infection during the COVID-19 Pandemic in Japan
6. 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
7. Characteristic genetic spectrum of primary ciliary dyskinesia in Japanese patients and global ethnic heterogeneity: population-based genomic variation database analysis
8. Congenital Cytomegalovirus Infection and Maternal Primary Cytomegalovirus Infection in Universal Newborn Hearing Screening Referral Patients: A Prospective Cohort Study
9. Evaluation of bleeding and anticoagulation markers by edoxaban and low‐dose cyclosporine: A case series study
10. A pediatric case of primary ciliary dyskinesia caused by novel copy number variation in PIH1D3
11. A Novel Homozygous Variant in GAS2L2 in Two Sisters with Primary Ciliary Dyskinesia
12. Primary ciliary dyskinesia with CCDC39 variants displaying specific ciliary ultrastructure and movement concordant with the genotype: A case report
13. Psychological characteristics of Japanese patients and their family members receiving genetic counseling: A single‐institute exploratory study
14. Dual Inhibition of CYP3A4 by Voriconazole and Clarithromycin Influences Tacrolimus Pharmacokinetics: Case Series Study
15. Succinate dehydrogenase B-deficient renal cell carcinoma with a germline variant in a Japanese patient: a case report
16. P52-5 Effort of Cancer Genome Center Hospital in Rural National University
17. Analysis of the diagnosis of Japanese patients with primary ciliary dyskinesia using a conditional reprogramming culture
18. Analysis of the clinical features of Japanese patients with primary ciliary dyskinesia
19. Precision cancer genome testing needs proficiency testing involving all stakeholders
20. A Pilot Proficiency Testing Study for Assessing Cancer Gene Panel using Patient Samples and Next-generation Sequencing in Japan
21. Primary cytomegalovirus infection during pregnancy and congenital infection: a population-based, mother–child, prospective cohort study
22. Multifaceted analysis of Japanese cases of primary ciliary dyskinesia: Value of immunofluorescence for ciliary protein detection in patients with DNAH5 and DNAH11 mutations
23. Characteristics and serology of pregnant women with cytomegalovirus immunoglobulin G seroconversion during pregnancy in Japan
24. Acquisition of JAK2 V617F to CALR‐mutated clones accelerates disease progression and might enhance growth capacity
25. MPL exon 10 mutations other than canonical MPL W515L/K mutations identified by in-house MPL exon 10 direct sequencing in essential thrombocythemia
26. A pediatric case of productive cough caused by novel variants in DNAH9
27. Development of cutaneous squamous cell carcinoma during pembrolizumab therapy
28. Risk factors for cisplatin‑induced acute kidney injury: A pilot study on the usefulness of genetic variants for predicting nephrotoxicity in clinical practice
29. Abstract TP229: Cerebral Venous Thrombosis Caused by Congenital Thrombophilia in Japan
30. miR‑3940‑5p/miR‑8069 ratio in urine exosomes is a novel diagnostic biomarker for pancreatic ductal adenocarcinoma
31. Copy number variation in DRC1 is the major cause of primary ciliary dyskinesia in the Japanese population
32. Usefulness of the APTT waveform for the diagnosis of DIC and prediction of the outcome or bleeding risk
33. Elevated plasma levels of soluble C-type lectin-like receptor 2 (CLEC2) in patients with thrombotic microangiopathy
34. A substitution in the pre-S1 promoter region is associated with the viral regulation of hepatitis B virus
35. Routine measurements of factor VIII activity and inhibitor titer in the presence of emicizumab utilizing anti‐idiotype monoclonal antibodies: comment
36. Comments to: An Evaluation of Hemostatic Abnormalities in Patients With Hemophilia by APTT Waveform, Peak Heights of APTT Waveform Are Useful for Diagnosing Hemophilia or Inhibitor
37. 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
38. A targeted next-generation sequencing panel reveals novel mutations in Japanese patients with primary ciliary dyskinesia
39. Clinical Manifestation of Patients With Atypical Hemolytic Uremic Syndrome With the C3 p.I1157T Variation in the Kinki Region of Japan
40. An Evaluation of Hemostatic Abnormalities in Patients With Hemophilia According to the Activated Partial Thromboplastin Time Waveform
41. Analysis of Otologic Features of Patients With Primary Ciliary Dyskinesia
42. Comparison of three different anti-Xa assays in major orthopedic surgery patients treated with direct oral anticoagulant
43. An Evaluation of the Activated Partial Thromboplastin Time Waveform
44. A case of dichorionic diamniotic twin pregnancy suspected with primary cytomegalovirus infection by maternal cytomegalovirus serological screening
45. Whole-exome sequencing identification of novel DNAH5 mutations in a young patient with primary ciliary dyskinesia
46. High prevalence of congenital thrombophilia in patients with pregnancy-related or idiopathic venous thromboembolism/pulmonary embolism
47. Hypofibrinogenemia and the α-Fibrinogen Thr312Ala Polymorphism may be Risk Factors for Early Pregnancy Loss
48. Protection From Pregnancy Loss in Women With Hereditary Thrombophilia When Associated With Fibrinogen Polymorphism Thr331Ala
49. Comparison of three different anti-Xa assays in major orthopedic surgery patients treated with fondaparinux
50. Plasma ADAMTS13, von Willebrand Factor (VWF), and VWF Propeptide Profiles in Patients With Connective Tissue Diseases and Antiphospholipid Syndrome
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