1,235 results on '"Takahashi, Masanori"'
Search Results
2. Efficacy confirmation study of aceneuramic acid administration for GNE myopathy in Japan
3. Switching disease-modifying therapies from sphingosine-1-phosphate receptor modulators to natalizumab or dimethyl fumarate restores immune responses after SARS-CoV-2 mRNA vaccination in patients with multiple sclerosis
4. Worsening of myasthenic symptoms associated with statins
5. Impact of Early Treatment with Intravenous High-Dose Methylprednisolone for Ocular Myasthenia Gravis
6. Erythromycin for myotonic dystrophy type 1: a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial
7. Clinical features and outcomes of patients with muscle-specific kinase antibody-positive myasthenia gravis in Japan
8. Taste disorders and alopecia in myasthenia gravis
9. Safety and efficacy of aceneuramic acid in GNE myopathy: open-label extension study
10. Safety and efficacy of rozanolixizumab in patients with generalised myasthenia gravis (MycarinG): a randomised, double-blind, placebo-controlled, adaptive phase 3 study
11. Safety and efficacy of zilucoplan in patients with generalised myasthenia gravis (RAISE): a randomised, double-blind, placebo-controlled, phase 3 study
12. Hyperkalemic periodic paralysis associated with a novel missense variant located in the inner pore of Nav1.4
13. Determination of Parameters for Sliding Mode Control using TD3
14. Données en vie réelle de l’utilisation d’éculizumab chez des patients japonais atteints de myasthénie grave : données de surveillance post-commercialisation
15. Facioscapulohumeral muscular dystrophy Health Index: Japanese translation and validation study
16. Design of Auxiliary Signals to Improve Performance of Self-repairing PID Control
17. Quality of life and subjective symptom impact in Japanese patients with myotonic dystrophy type 1
18. Bottom-up processes drive reproductive success of Japanese anchovy in an oligotrophic sea: A case study in the central Seto Inland Sea, Japan
19. Characteristics of myotonic dystrophy patients in the national registry of Japan
20. Lineage tracing using Wnt2b‐2A‐CreERT2 knock‐in mice reveals the contributions of Wnt2b‐expressing cells to novel subpopulations of mesothelial/epicardial cell lineages during mouse development.
21. Therapeutic Responses to Efgartigimod for Generalized Myasthenia Gravis in Japan.
22. Design and Applications of Highly Nonlinear Fibers
23. Standard Coating Diameter Uncoupled 19-Core Multicore Fiber with Highest Core Density for Optical Wiring
24. Fiber Bundle Fan-in/Fan-out (FIFO) for Coupled MCF with High- 4-Core Fiber Pitch Converter
25. An Event-triggered Control System to Detect Network Disconnection
26. A web-based questionnaire survey on the influence of coronavirus disease-19 on the care of patients with muscular dystrophy
27. Erythromycin for myotonic dystrophy type 1: a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial
28. Metabolic complications in myotonic dystrophy type 1: A cross-sectional survey using the National Registry of Japan
29. Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT): a multicentre, randomised, placebo-controlled, phase 3 trial
30. Factors affecting short-term functional gain following total knee arthroplasty in patients aged from 75 years at a postacute rehabilitation setting
31. Clinical Features of Skeletal Muscle and Their Underlying Molecular Mechanism
32. Real‐world experience with eculizumab and switching to ravulizumab for generalized myasthenia gravis.
33. Self-repairing Control against Actuator Failures Using a Spiking Neuron Model
34. The practice of active patient involvement in rare disease research using ICT: experiences and lessons from the RUDY JAPAN project
35. Analysis of the genetic background associated with sporadic periodic paralysis in Japanese patients
36. RGMa collapses the neuronal actin barrier against disease-implicated protein and exacerbates ALS
37. Longitudinal Changes in Neuropsychological Functioning in Japanese Patients with Myotonic Dystrophy Type 1: A Five Year Follow-Up Study
38. Data-driven Response Estimation-based Tuning and its Validation Using a Ball-and-Beam System
39. two-step detection method for actuator and sensor failures based on self-repairing PID control
40. Long-term efficacy and safety of eculizumab in Japanese patients with generalized myasthenia gravis: A subgroup analysis of the REGAIN open-label extension study
41. Functional analysis of a double-point mutation in the KCNJ2 gene identified in a family with Andersen-Tawil syndrome
42. Izhikevich Model-based Self-repairing Control for Plants with Sensor Failures and Disturbances
43. Simple Adaptive Control Against Sensor Failures
44. Rigorous evaluation of genetic and epigenetic effects on clinical laboratory measurements using Japanese monozygotic twins.
45. Phase II/III Study of Aceneuramic Acid Administration for GNE Myopathy in Japan
46. Optical measurement of gating pore currents in hypokalemic periodic paralysis model cells
47. Cardiac Emerinopathy: A Non-syndromic Nuclear Envelopathy with Increased Risk of Thromboembolic Stroke due to Progressive Atrial Standstill and Left Ventricular Non-compaction
48. Self-repairing Adaptive PID Control for Plants with Sensor Failures
49. Human Mesenchymal Stem Cells in Rodent Whole-Embryo Culture Are Reprogrammed to Contribute to Kidney Tissues
50. Downstream genes of Pax6 revealed by comprehensive transcriptome profiling in the developing rat hindbrain
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