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1. Heterozygous mutations in the straitjacket region of the latency-associated peptide domain of TGFB2 cause Camurati–Engelmann disease type II

4. Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans.

5. Predictors for Vulnerable Plaque in Functionally Significant Lesions

6. Vascular Remodeling in Coronary Microvascular Dysfunction

9. Phenotypic and mutational spectrum of ROR2‐related Robinow syndrome

12. Loss of function in NSD2 causes DNA methylation signature similar to that in Wolf-Hirschhorn syndrome

13. Continuous vs Bolus Thermodilution to Assess Microvascular Resistance Reserve

14. Coronary Atherosclerosis Phenotypes in Focal and Diffuse Disease

15. Impact of Post-PCI FFR Stratified by Coronary Artery

16. Five-Year Outcomes After Fractional Flow Reserve–Guided Deferral of Revascularization in Infarct-Related Artery Lesions

17. PFML-based Semantic BCI Agent for Game of Go Learning and Prediction

27. High diagnostic yield in skeletal ciliopathies using massively parallel genome sequencing, structural variant screening and RNA analyses

28. Potential anti-COVID-19 agents, cepharanthine and nelfinavir, and their usage for combination treatment

31. Rheocarna Effectively Treats Oral Medicinal Therapy‐Resistant Cutaneous Symptoms and Renal Failure Induced by Cholesterol Crystal Embolism.

34. Stent sizing by coronary CT angiography compared with optical coherence tomography

35. Impact of vessel volume on thermodilution measurements in patients with coronary microvascular dysfunction

36. Idiopathic pulmonary hemosiderosis associated with Kabuki syndrome.

37. The machinery for endocytosis of epidermal growth factor receptor coordinates the transport of incoming hepatitis B virus to the endosomal network

43. Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation

45. List of contributors

46. R&D on commercial high temperature gas-cooled reactor

49. Genetic abnormalities in a large cohort of Coffin–Siris syndrome patients

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