223 results on '"Torisu, Hiroyuki"'
Search Results
2. Heterogeneity and mitochondrial vulnerability configurate the divergent immunoreactivity of human induced microglia-like cells
3. Shank3a/b isoforms regulate the susceptibility to seizures and thalamocortical development in the early postnatal period of mice
4. A nation-wide survey of Japanese pediatric MOG antibody-associated diseases
5. PRRT2 mutations in Japanese patients with benign infantile epilepsy and paroxysmal kinesigenic dyskinesia
6. Serial MRI findings of acute flaccid myelitis during an outbreak of enterovirus D68 infection in Japan
7. Neurodevelopmental Outcomes of High-Risk Preterm Infants: A Prospective Study in Japan
8. Leucine-rich alpha-2 glycoprotein in the cerebrospinal fluid is a potential inflammatory biomarker for meningitis
9. Clinical Features of Acute Flaccid Myelitis Temporally Associated With an Enterovirus D68 Outbreak : Results of a Nationwide Survey of Acute Flaccid Paralysis in Japan, August–December 2015
10. A male case with CDKL5-associated encephalopathy manifesting transient methylmalonic acidemia
11. Epidemiology of Acute Disseminated Encephalomyelitis
12. List of Contributors
13. Altered strategy in short-term memory for pictures in children with attention-deficit/hyperactivity disorder: A near-infrared spectroscopy study
14. Strategy in short-term memory for pictures in childhood: A near-infrared spectroscopy study
15. Clinical and MRI characteristics of acute encephalopathy in congenital adrenal hyperplasia
16. Clinical and electrophysiological features of acute flaccid myelitis: A national cohort study
17. Favorable outcomes of interferon-α and ribavirin treatment for a male with subacute sclerosing panencephalitis
18. De novo ATP1A3 variants cause polymicrogyria
19. Three-Year Longitudinal Motor Function and Disability Level of Acute Flaccid Myelitis
20. PD1 as a common candidate susceptibility gene of subacute sclerosing panencephalitis
21. Association of toll-like receptor 3 gene polymorphism with subacute sclerosing panencephalitis
22. Gene expression profiles in peripheral blood mononuclear cells from patients with subacute sclerosing panencephalitis using oligonucleotide microarrays
23. Founder effect of the C9 R95X mutation in Orientals
24. Parental age and child growth and development: Child health check-up data
25. Neurodevelopmental Outcomes of High-Risk Preterm Infants
26. Interleukin-10 is associated with resistance to febrile seizures: Genetic association and experimental animal studies
27. Genetic susceptibility to febrile seizures in Japanese, studies on TNFα, IL-6, IL-8, IL-1B, and IL-10 genes: O-023
28. Chapter 19 - Epidemiology of Acute Disseminated Encephalomyelitis
29. Rhombencephalitis and coxsackievirus A16
30. An acute encephalopathy with reduced diffusion in BRAF-associated cardio-facio-cutaneous syndrome
31. Vaccination-associated acute disseminated encephalomyelitis
32. A Nationwide Survey of Pediatric-onset Japanese Encephalitis in Japan
33. Additional file 1: of Sustained endocrine profiles of a girl with WAGR syndrome
34. Early-onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2
35. Sustained endocrine profiles of a girl with WAGR syndrome
36. Transient dysautonomia in an acute phase of encephalopathy with biphasic seizures and late reduced diffusion
37. Involuntary movements and coma as the prognostic marker for acute encephalopathy with biphasic seizures and late reduced diffusion
38. De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis
39. Nationwide Survey of Pediatric-onset Japanese Encephalitis in Japan.
40. Girl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes
41. Neuroendocrine phenotypes in a boy with 5q14 deletion syndrome implicate the regulatory roles of myocyte-specific enhancer factor 2C in the postnatal hypothalamus
42. A case of childhood stiff-person syndrome with striatal lesions: A possible entity distinct from the classical adult form
43. Alexander disease with mild dorsal brainstem atrophy and infantile spasms
44. Periodic Epileptiform Discharges in Children With Advanced Stages of Progressive Myoclonic Epilepsy
45. De NovoTruncating Mutation ofTRIM8Causes Early-Onset Epileptic Encephalopathy
46. Correction: Corrigendum: Hyperactive mTOR signals in the proopiomelanocortin-expressing hippocampal neurons cause age-dependent epilepsy and premature death in mice
47. Hyperactive mTOR signals in the proopiomelanocortin-expressing hippocampal neurons cause age-dependent epilepsy and premature death in mice
48. Analysis of Death Due to Infectious Diseases in Patients Hospitalized in the Pediatric Ward of a Single Japanese Tertiary Medical Facility
49. Early‐onset epileptic encephalopathy and severe developmental delay in an association with de novo double mutations in NF1 and MAGEL2.
50. Clinical Features of Acute Flaccid Myelitis Temporally Associated With an Enterovirus D68 Outbreak: Results of a Nationwide Survey of Acute Flaccid Paralysis in Japan, August-December 2015.
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