265 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. Cytomegalovirus DNA Loads in Organs of Congenitally Infected Fetus
9. Primary cytomegalovirus infection during pregnancy and congenital infection: a population-based, mother–child, prospective cohort study
10. MPL exon 10 mutations other than canonical MPL W515L/K mutations identified by in-house MPL exon 10 direct sequencing in essential thrombocythemia
11. Cytomegalovirus DNA Loads in Organs of Congenitally Infected Fetus.
12. MO16-3 Clinical relevance of comprehensive genome profiling using real-world data in colorectal cancer
13. A pediatric case of productive cough caused by novel variants in DNAH9
14. Analysis of clinical features of Japanese patients with primary ciliary dyskinesia
15. P1061: CLINICAL FEATURES OF PHILADELPHIA-NEGATIVE MPN DEVELOPED IN ADOLESCENTS AND YOUNG ADULTS IN JAPAN
16. Transient Decrease in Incidence Rate of Maternal Primary Cytomegalovirus Infection during the COVID-19 Pandemic in Japan
17. 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
18. A 3000-year-old founder variant in the DRC1gene causes primary ciliary dyskinesia in Japan and Korea
19. Usefulness of the APTT waveform for the diagnosis of DIC and prediction of the outcome or bleeding risk
20. A substitution in the pre-S1 promoter region is associated with the viral regulation of hepatitis B virus
21. Congenital Cytomegalovirus Infection and Maternal Primary Cytomegalovirus Infection in Universal Newborn Hearing Screening Referral Patients: A Prospective Cohort Study
22. High prevalence of congenital thrombophilia in patients with pregnancy-related or idiopathic venous thromboembolism/pulmonary embolism
23. Evaluation of bleeding and anticoagulation markers by edoxaban and low‐dose cyclosporine: A case series study
24. A pediatric case of primary ciliary dyskinesia caused by novel copy number variation in PIH1D3
25. A Novel Homozygous Variant in GAS2L2 in Two Sisters with Primary Ciliary Dyskinesia
26. Primary ciliary dyskinesia with CCDC39 variants displaying specific ciliary ultrastructure and movement concordant with the genotype: A case report
27. Psychological characteristics of Japanese patients and their family members receiving genetic counseling: A single‐institute exploratory study
28. Elevated plasma levels of soluble platelet glycoprotein VI (GPVI) in patients with thrombotic microangiopathy
29. 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
30. Analysis of Otologic Features of Patients With Primary Ciliary Dyskinesia
31. Comparison of three different anti-Xa assays in major orthopedic surgery patients treated with fondaparinux
32. P52-5 Effort of Cancer Genome Center Hospital in Rural National University
33. Psychological characteristics of Japanese patients and their family members receiving genetic counseling: A single‐institute exploratory study.
34. High frequency of decreased antithrombin level in pregnant women with thrombosis
35. Analysis of the clinical features of Japanese patients with primary ciliary dyskinesia
36. Analysis of patients with atypical hemolytic uremic syndrome treated at the Mie University Hospital: concentration of C3 p.I1157T mutation
37. Clinical features and underlying causes of cerebral venous thrombosis in Japanese patients
38. Analysis three abnormal Protein S genes in a patient with pulmonary embolism
39. A Pilot Proficiency Testing Study for Assessing Cancer Gene Panel using Patient Samples and Next-generation Sequencing in Japan
40. Presence of antiphospholipid antibody is a risk factor in thrombotic events in patients with antiphospholipid syndrome or relevant diseases
41. Multifaceted analysis of Japanese cases of primary ciliary dyskinesia: Value of immunofluorescence for ciliary protein detection in patients with DNAH5 and DNAH11 mutations
42. Characteristics and serology of pregnant women with cytomegalovirus immunoglobulin G seroconversion during pregnancy in Japan
43. Acquisition of JAK2 V617F to CALR‐mutated clones accelerates disease progression and might enhance growth capacity
44. Frequent association of thrombophilia in cerebral venous sinus thrombosis
45. The association of protein S Tokushima-K196E with a risk of deep vein thrombosis
46. Congenital Thrombophilia in Patients With Superior Mesenteric Venous Thrombosis or Portal Vein Thrombosis
47. Des-γ-carboxy prothrombin ratio measured by P-11 and P-16 antibodies is a novel biomarker for hepatocellular carcinoma
48. Primary ciliary dyskinesia with CCDC39variants displaying specific ciliary ultrastructure and movement concordant with the genotype: A case report
49. Development of cutaneous squamous cell carcinoma during pembrolizumab therapy
50. Risk factors for cisplatin‑induced acute kidney injury: A pilot study on the usefulness of genetic variants for predicting nephrotoxicity in clinical practice
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