44 results on '"Takeshita E"'
Search Results
2. A fluorescent screen + CCD system for quality assurance of therapeutic scanned ion beams
3. Development of beam current control system in RF-knockout slow extraction
4. Recent progress on new treatment research project at HIMAC
5. Spreading of a heavy ion beam with the dual-ring double scattering method
6. Beam stability improvement of the HIMAC synchrotron using a feed-forward system for magnet power supplies
7. Multiple-energy operation with extended flattops at HIMAC
8. P.123 A Phase I/II study of NS-089/NCNP-02, Exon 44 skipping drug, in patients with Duchenne muscular dystrophy
9. WITHDRAWN: Beam position alignment and its verification for therapeutic ion beams from synchrotron
10. FSHD: EP.167 Longitudinal clinical course of early-onset facioscapulohumeral muscular dystrophy
11. DMD – CLINICAL CARE: EP.102 Clinical characteristics of early-onset cardiomyopathy in patients with Duchenne muscular dystrophy
12. CONGENITAL MUSCULAR DYSTROPHIES: EP.64 Brain image phenotypes and developmental milestones in Fukuyama congenital muscular dystrophy
13. REGISTRIES, CARE, QUALITY OF LIFE, MANAGEMENT OF NMD: P.337 Variability of cardiac function in patients with Duchenne muscular dystrophy experiencing sudden onset chest pain and electrocardiographic changes
14. SMA - CLINICAL: P.84 Magnetic resonance imaging of muscle and motor functional changes in patients with spinal muscular atrophy treated with nusinersen
15. P.373Longitudinal changes in electrophysiological findings caused by nusinersen administration in patients with spinal muscular atrophy type 2 or type 3
16. P.344Assessment of longitudinal developmental milestones in Fukuyama congenital muscular dystrophy
17. P.230Phenotype and pathological variability in RYR1-related myopathy with compound heterozygous variants in Japan
18. E-POSTERS – MITOCHONDRIAL / METABOLIC DISEASES –CASE REPORTS: EP.01Becker muscular dystrophy with acid α-glucosidase pseudodeficiency
19. METABOLIC DISTURBANCES IN NEUROMUSCULAR DISEASES: O.1Bi-allelic mutations in COX6A2 cause a striated muscle-specific cytochrome c oxidase deficiency
20. Retraction notice to "Beam position alignment and its verification for therapeutic ion beams from synchrotron" [NIM B 406PA (2017) 368–373]
21. DUCHENNE MUSCULAR DYSTROPHY – CLINICAL: P.29Analysis of respiratory function of Duchenne muscular dystrophy with Chilaiditi syndrome
22. High-risk screening for late-onset Pompe disease in Japan
23. P.405 - A Phase I, single- and repeated-dose study of TAS-205, a novel inhibitor of hematopoietic prostaglandin D synthase, in patients with Duchenne muscular dystrophy
24. P.212 - Screening for late-onset Pompe disease among high-risk population in Japan
25. P.91 - Quantitative analysis of muscle resonance imaging of fatty infiltration of the pelvic and lower limb muscles in Duchenne muscular dystrophy using excel based auto calculation program
26. P.32 - Electrophysiological and pathological studies of peripheral nerves in children with merosin-deficient congenital muscular dystrophy type 1A
27. P.199 - Signal abnormalities of muscle and fascia in muscular MRI imaging at pretreatment stage in children with juvenile dermatomyositis
28. P.30 - IBIC-LG: Selectivity pattern of muscular MRI images in limb-girdle muscular dystrophy (LGMD) 2A using database of skeletal muscular images
29. Muscular dystrophy clinical trial network: establishment and promotion of clinical research for neuromuscular diseases in Japan
30. G.P.262 - Early scoliosis surgery may prevent deterioration of respiratory function in Ullrich congenital muscular dystrophy
31. G.P.251 - Exon 53 skipping of the dystrophin gene in patients with Duchenne muscular dystrophy by systemic administration of NS-065/NCNP-01: A phase 1, dose escalation, first-in-human study
32. G.P.27 - Type-specific selectivity pattern of skeletal muscle images in spinal muscular atrophy
33. G.P.262: Selectivity patterns on lower limb skeletal muscle imaging in patients with nemaline myopathy
34. G.P.179: Association between resting energy expenditure and body weight change in patients with Duchenne muscular dystrophy
35. G.P.47 Congenital generalized lipodystrophy type 4 with muscular dystrophy: Clinical manifestations in early childhood
36. Shape transition observed in neutron-rich pf-shell isotopes studied via proton inelastic scattering
37. METABOLIC MYOPATHIES II: P.348Identification of late-onset Pompe disease with nationwide high-risk screening study in Japan.
38. Search for low lying dipole strength in the neutron rich nucleus 26Ne
39. Proton Shell Structure in Neutron-rich 23F
40. Proton single-particle states in the neutron-rich 23F nucleus
41. Search for an isomeric state in 19C.
42. Excited states in neutron rich boron isotopes
43. FSHD / OPMD / EDMD / DMI: P.368Clinical characteristics of 4 patients with childhood-onset reducing body myopathy in Japan.
44. CONGENITAL MUSCULAR DYSTROPHIES: P.328Pneumothorax in Ullrich congenital muscular dystrophy.
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