138 results on '"Sugai, Kenji"'
Search Results
2. Postoperative improvement of executive function and adaptive behavior in children with intractable epilepsy
3. The effect of the guidelines for management of febrile seizures 2015 on clinical practices: Nationwide survey in Japan
4. Disrupted cortico-ponto-cerebellar pathway in patients with hemimegalencephaly
5. Efficacy, safety, and pharmacokinetics of intravenous midazolam in Japanese children with status epilepticus
6. Urinary prostaglandin metabolites as Duchenne muscular dystrophy progression markers
7. New guidelines for management of febrile seizures in Japan
8. Long-term outcomes of steroid therapy for Duchenne muscular dystrophy in Japan
9. Surgical versus medical treatment for children with epileptic encephalopathy in infancy and early childhood: Results of an international multicenter cohort study in Far-East Asia (the FACE study)
10. The long-term health impact and potential predictors of cardiopulmonary arrest in patients with childhood-onset psychomotor impairments
11. Three cases of right frontal megalencephaly: Clinical characteristics and long-term outcome
12. Episodic tremors representing cortical myoclonus are characteristic in Angelman syndrome due to UBE3A mutations
13. Correlation of augmented startle reflex with brainstem electrophysiological responses in Tay–Sachs disease
14. Hypophosphatemia is a common complication in severely disabled individuals with neurological disorders and is caused by infection, refeeding and Fanconi syndrome
15. Evaluation of FDG-PET and ECD-SPECT in patients with subcortical band heterotopia
16. Surgical management of cortical dysplasia in infancy and early childhood
17. Clinical analysis of catastrophic epilepsy in infancy and early childhood: Results of the Far-East Asia Catastrophic Epilepsy (FACE) study group
18. Immunomodulatory therapy versus surgery for Rasmussen syndrome in early childhood
19. Unusual exocrine complication of pancreatitis in mitochondrial disease
20. Late-onset epilepsy in children with acute febrile encephalopathy with prolonged convulsions: A clinical and encephalographic study
21. Peripheral nerve abnormalities in pediatric patients with spinal muscular atrophy
22. Decreased resting energy expenditure in patients with Duchenne muscular dystrophy
23. Inflammatory changes in infantile-onset LMNA-associated myopathy
24. Effects of low-dose hydrochlorothiazide on urolithiasis and bone metabolism in severely disabled individuals: A pilot study
25. Evolution of hemiplegic attacks and epileptic seizures in alternating hemiplegia of childhood
26. Treatment of epilepsy in severely disabled children with bilateral brain malformations
27. Reassessment of phenytoin for treatment of late stage progressive myoclonus epilepsy complicated with status epilepticus
28. Activation of microglia/macrophages expressing phosphorylated S6 ribosomal protein in a case of hemimegalencephaly with progressive calcification and atrophy
29. KCNT1-positive epilepsy of infancy with migrating focal seizures successfully treated with nonnarcotic antitussive drugs after treatment failure with quinidine: A case report
30. Variant in the neuronal vesicular SNARE VAMP2 (synaptobrevin-2): First report in Japan
31. Effects of clonazepam on self-induced photoparoxysmal responses
32. MELAS phenotype associated with m.3302A>G mutation in mitochondrial tRNALeu(UUR) gene
33. Persistent verbal and behavioral deficits after resection of the left supplementary motor area in epilepsy surgery
34. MRI, MR spectroscopy, and diffusion tensor imaging findings in patient with static encephalopathy of childhood with neurodegeneration in adulthood (SENDA)
35. Two Japanese cases of epileptic encephalopathy associated with an FGF12 mutation
36. O-2-24. Multimodal evoked potential study following posterior quadrantectomy in children with intractable epilepsy
37. Epileptic apnea in a patient with inherited glycosylphosphatidylinositol anchor deficiency and PIGT mutations
38. Focal cortical myoclonus in rolandic cortical dysplasia presenting as hemifacial twitching
39. A pediatric patient with myopathy associated with antibodies to a signal recognition particle
40. A case of bulbar type cerebral palsy: Representative symptoms of dorsal brainstem syndrome
41. Muscle glycogen storage disease 0 presenting recurrent syncope with weakness and myalgia
42. A novel mutation in the LMNA gene causes congenital muscular dystrophy with dropped head and brain involvement
43. Concurrence of multiple types of eyelid synkinesia in a patient with congenital anomalies
44. Late-onset mental deterioration and fluctuating dystonia in a female patient with a truncating MECP2 mutation
45. Effects of acetazolamide on epileptic apnea in migrating partial seizures in infancy
46. CD4 +CD25 high regulatory T cell in childhood ocular myasthenia gravis
47. Polymicrogyria and infantile spasms in a patient with 1p36 deletion syndrome
48. Augmented startle responses in opsoclonus-myoclonus syndrome
49. Cardio-facio-cutaneous syndrome with infantile spasms and delayed myelination
50. Acute autonomic sensory and motor neuropathy associated with parvovirus B19 infection
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