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5. Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia

8. Incidence and Expected Probability of Liver Cirrhosis and Hepatocellular Carcinoma After Fontan Operation

13. The c.1617del variant of TMEM260is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease

19. Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy

20. Categorized and Integrated Data Mining of Medical Data from the Viewpoint of Chance Discovery

21. Categorized and Integrated Data Mining of Medical Data

22. Data Mining of Multi-categorized Data

25. An Interface for Medical Diagnosis Support

27. Predictors of liver cirrhosis and hepatocellular carcinoma among perioperative survivors of the Fontan operation

28. CORRIGENDUM: Outcomes of Dilated Cardiomyopathy in Japanese Children ― A Retrospective Cohort Study ―

29. Outcomes of Childhood Pulmonary Arterial Hypertension in BMPR2 and ALK1 Mutation Carriers

30. Functional Evaluation of Human Bioengineered Cardiac Tissue Using iPS Cells Derived from a Patient with Lamin Variant Dilated Cardiomyopathy

31. Distinct Function of 2 Chromatin Remodeling Complexes That Share a Common Subunit, Williams Syndrome Transcription Factor (WSTF)

32. Predictors of long-term mortality among perioperative survivors of Fontan operation

33. Outcomes of hypertrophic cardiomyopathy in Japanese children: a retrospective cohort study

34. Induced Pluripotent Stem Cell-Derived Cardiomyocytes with SCN5A R1623Q Mutation Associated with Severe Long QT Syndrome in Fetuses and Neonates Recapitulates Pathophysiological Phenotypes

36. Outcomes of Dilated Cardiomyopathy in Japanese Children ― A Retrospective Cohort Study ―

37. Predictors of liver cirrhosis and hepatocellular carcinoma among perioperative survivors of the Fontan operation

38. Predictors of long-term mortality among perioperative survivors of Fontan operation.

40. Pregnancy and Delivery in Patients With Repaired Congenital Heart Disease ― A Retrospective Japanese Multicenter Study ―

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