97 results on '"Sasaki, M."'
Search Results
2. P.123 A Phase I/II study of NS-089/NCNP-02, Exon 44 skipping drug, in patients with Duchenne muscular dystrophy
3. DMD – CLINICAL CARE
4. CONGENITAL MUSCULAR DYSTROPHIES
5. FSHD
6. REGISTRIES, CARE, QUALITY OF LIFE, MANAGEMENT OF NMD
7. SMA - CLINICAL
8. P.230Phenotype and pathological variability in RYR1-related myopathy with compound heterozygous variants in Japan
9. P.344Assessment of longitudinal developmental milestones in Fukuyama congenital muscular dystrophy
10. E-POSTERS – MITOCHONDRIAL / METABOLIC DISEASES –CASE REPORTS
11. DUCHENNE MUSCULAR DYSTROPHY – CLINICAL
12. FSHD / OPMD / EDMD / DMI
13. FSHD: EP.167 Longitudinal clinical course of early-onset facioscapulohumeral muscular dystrophy
14. DMD – CLINICAL CARE: EP.102 Clinical characteristics of early-onset cardiomyopathy in patients with Duchenne muscular dystrophy
15. CONGENITAL MUSCULAR DYSTROPHIES: EP.64 Brain image phenotypes and developmental milestones in Fukuyama congenital muscular dystrophy
16. Risk factors for nerve injury after total knee arthroplasty: a case control study
17. Risk factors for nerve injury after total hip arthroplasty: a case control study
18. Electrophysiological and pathological studies of peripheral nerves in children with merosin-deficient congenital muscular dystrophy type 1A
19. 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
20. 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
21. Registry of congenital neuromuscular disorders in Japan: establishment and implementation
22. Incidence and risk factors for neuropathy following primary total knee arthroplasty
23. Incidence and risk factors for neuropathy following primary total hip arthroplasty
24. Signal abnormalities of muscle and fascia in muscular MRI imaging at pretreatment stage in children with juvenile dermatomyositis
25. IBIC-LG: Selectivity pattern of muscular MRI images in limb-girdle muscular dystrophy (LGMD) 2A using database of skeletal muscular images
26. Type-specific selectivity pattern of skeletal muscle images in spinal muscular atrophy
27. Early scoliosis surgery may prevent deterioration of respiratory function in Ullrich congenital muscular dystrophy
28. 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
29. Mutations in iron–sulfur cluster assembly gene IBA57 cause progressive cavitating leukoencephalopathy
30. P.102 - Registry of congenital neuromuscular disorders in Japan: establishment and implementation
31. 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
32. P.32 - Electrophysiological and pathological studies of peripheral nerves in children with merosin-deficient congenital muscular dystrophy type 1A
33. G.P.76
34. G.P.179
35. G.P.262
36. PN12 - Incidence and risk factors for neuropathy following primary total knee arthroplasty
37. PN11 - Incidence and risk factors for neuropathy following primary total hip arthroplasty
38. P.199 - Signal abnormalities of muscle and fascia in muscular MRI imaging at pretreatment stage in children with juvenile dermatomyositis
39. P.30 - IBIC-LG: Selectivity pattern of muscular MRI images in limb-girdle muscular dystrophy (LGMD) 2A using database of skeletal muscular images
40. P.1.1 Natural history of Ullrich congenital muscular dystrophy
41. G.P.127 A nation-wide survey for Marinesco-Sjögren syndrome
42. C.P.4 Congenital fiber type disproportion with myofibrillar disorganization and altered internal nuclei is caused by RYR1 mutation
43. G.P.262 - Early scoliosis surgery may prevent deterioration of respiratory function in Ullrich congenital muscular dystrophy
44. 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
45. G.P.60 - Mutations in iron–sulfur cluster assembly gene IBA57 cause progressive cavitating leukoencephalopathy
46. G.P.27 - Type-specific selectivity pattern of skeletal muscle images in spinal muscular atrophy
47. P1.37 Total energy expenditure (TEE) of patients with Duchenne muscular dystrophy
48. P4.45 Muscle glycogen storage disease type 0b presenting recurrent post-exercise loss of consciousness with weakness and myalgia
49. P4.30 Muscle MRI of spinal muscular atrophy
50. P2.23 Congenital form of X-linked myopathy with excessive autophagy associated with VMA21 mutation
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